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متلازمة القولون المتهيج بين طلاب المدارس الثانوية : نسبة الانتشار والاسباب 2017 - 2018 == Irritable Bowel Syndrome Among High School Students : Prevalence and Determinants 2017 - 2018

Author name: هناء فريق هزاع
Supervisor name: فارس حسن اللامي
General topic: Medicine
Specific topic: Community Medicine
Degree: Master
Language: English
University location: Baghdad
First pages:
Abstract: الخلفية : ان متلازمة القولون المتهيج هي خلل وظيفي يصيب الامعاء الغليظة ويؤدي الى اعراض مزمنة في الجهاز الهضمي. وهو مرض واسع الانتشار يصيب كل الفئات العمرية لكنه اوسع انتشارا" بين فئة المراهقين والشباب.الهدف من الدراسة : هو معرفة نسبة انتشار المرض بين طلاب المدارس الثانوية وتحديد العوامل المؤثرة في زيادة نسبة انتشاره في محافظة بغداد 2017 - 2018 الاشخاص وطريقة العمل : هذه دراسة مقطعية اجريت على 12 مدرسة من المدارس الثانوية التابعة لمديريات تربية بغداد \ الكرخ. حيث تمت الدراسة عن طريق الاستبيان المباشرلاعراض المرض لجميع طلاب المرحلة السادسة في تلك المدارس , ذكورا"واناثا". وقد تم استبعاد الطلبة الذين يعانون من الاعراض التي تشير الى امراض اخرى قد تتداخل مع تشخيص المرض., وكذلك استبعاد الطلبة الذين سبق وان اجروا عملية سابقة او شخصوا باصابتهم بامراض اخرى في الجهاز الهضمي وقد تمت الدراسة بتطبيق نوعين مختلفين من الاستبيان, الاول لجمع المعلومات الاجتماعية والديموغرافية والعادات اليومية للطلبة, والاستبيان الثاني (Rome Criteria III) لتشخيص المرض ,ثم تصنيفه الى ثلاثة انواع (رابط الاسهال, رابط الامساك ,النوع المختلط) النتائج : شملت الدراسة 592 طالب وطالبة, وقد اظهرت الدراسة ان النسبة العامة لانتشارالمرض كانت 29,7% (فاصل الثقة 95% 29.4 - 30.1%) مع نسبة اعلى للانتشار بين الاناث عن الذكور بنسبة1 : 1.5 كما اظهرت الدراسة ان النوع المختلط من المرض هو النوع الاكثر شيوعا"(42.6%) يليه رابط الاسهال(33.5%), ثمرابط الامساك(23.9%). وكشف معامل الانحدار اللوجستي عوامل الخطورة التالية : الضغوط الحياتية) 3.93% (OR= والحساسية للاطعمة (2.89% OR=) والامراض المزمنة (2.22% (OR= والعامل الوراثي (2.04% OR=) والجنس (1.84% OR=) هي من اهم العوامل المؤثرة في زيادة نسبة انتشار المرض | Background : Irritable Bowel Syndrome (IBS) is a chronic functional gastrointestinal disorder. It's worldwide prevalent and causes a great challenge on the health system and patients' daily life activity. It affect all age groups but more common among adolescents and young age groups.Objectives : To estimate the prevalence and identify potential determinants of IBS among high school students in Baghdad, Iraq.Methods : This cross - sectional study was conducted on a cluster sample of 12 high schools in Baghdad. All students in the sixth grade were considered eligible. Students with "red flag" symptoms were excluded. Rome III criteria questionnaire was considered to define Irritable Bowel Syndrome. A self - administered questionnaire used to compile socio - demographics, personal habits and certain potential determinants.Statistical Analysis : Statistical Package for Social Sciences (SPSS) program, version 23 was used for data entry and analysis. The prevalence (and its 95% confidence interval) of Irritable Bowel Syndrome among high school students was calculated. Chi square and fisher's exact probability test were applied to test association of qualitative and categorical variables with IBS. Logistic regression analysis was used to identify the significant, independent and un - confounded risk factors.Result. Among 657 eligible high school students, 592 (90.1%) were enrolled. The prevalence of Irritable Bowel Syndrome was 29.7% (95% C.I. 29.4 - 30.1%). The most common type was mixed type (42.6%) followed by diarrhea - predominant (33.5%), then constipation - predominant (23.86%). Binary and logistic regression analyses revealed the following significant factors. Exposure to stressful life event (OR. 3.93; 95% CI. 2.64 - 4.85), food hypersensitivity (OR. 2.89; 95% CI. 1.59 - 3.27), chronic diseases (OR. 2.22; 95% CI. 1.24 - 3.95), family history of IBS (OR. 2.04;95% CI. 1.30 - 3.01) and female sex (OR. 1.84; 95% CI. 1.25 - 2.73). C - IBS was significantly more common among females (P=0.02) Conclusion : Irritable Bowel Syndrome is prevalent among high school students in Iraq, affected about one third of them. Stressful life events were the most important modified risk factor and it was the strongest factor affecting the prevalence of Irritable bowel syndrome. Food hypersensitivity, family history, chronic health problems and gender were the most important non - modified risk factors and Migraine was the most common comorbid chronic disease among students with Irritable Bowel Syndrome.

نتائج القسطرة القلبية لمرضى الذبحة القلبية المستقرة الذين لديهم تخطيط طبيعي او انسداد في الحزمة الكهربائية اليسرى او اليمنى == CORONARY ANGIOGRAPHIC FINDINGS IN PATIENTS WITH CHRONIC STABLE ANGINA AND NORMAL ECG, LBBB OR RBBB

Author name: زاهر عبد القادر حسين علي
Supervisor name: حسن علي الفرحان
General topic: Medicine
Specific topic: Diseases - Heart
Degree: Higher Diploma
Language: English
University location: Baghdad
First pages:
Abstract: الخلفية : الذبحة الصدرية المستقرة هي احد مظاهر الاصابة بامراض القلب في حوالي 20 الى 40٪ من المرضى ، والمريض النموذجي المصاب بالذبحة الصدرية يحدث في رجل اكبر من 50 عاما او امراة اكبر من 60 عاما من العمر ، والنتائج على مخطط القلب الكهربائي (ECG)قد يكون طبيعي في نصف المرضى الذين يعانون من الذبحة الصدرية المزمنة المستقرة. هدف الدراسة : لمعرفة نتائج القسطرة القلبية لمرضى الذبحة القلبية المستقرة الذين لديهم تخطيط طبيعي او انسداد في الحزمة الكهربائية اليسرى او اليمنى.المواد والعمل : اجريت دراسة مقطعية مستعرضة في المركز العراقي لامراض القلب. في الفترة من 15 يناير 2018 الى 15 يوليو 2018 والتي شملت المرضى الذين يعانون من الذبحة الصدرية المزمنة والمستقرة ولديهم تخطيط القلب كان طبيعيا او مع انسداد في الحزمة الكهربائية اليسرى او اليمنى. خضع جميع المرضى تخطيط صدى القلب, جميع المرضى قاموا بعمل تصوير الاوعية التاجية وتم اخذ البيانات من التقارير ، ثم التحليل الاحصائي.النتائج : في الدراسة الحالية ، كان متوسط عمر المرضى الذين كان تصوير الاوعية التاجية لهم غير طبيعي 57.7، وكان معظم المرضى من الذكور ، ومعظم المرضى كانوا من الذين يعانون من مرض السكري وكذلك معضم المرضى الذين لديهم تصوير الاوعية التاجية غير طبيعي كانوا لديهم علامات نموذجية لقصور الشرايين التاجية، والمرضى الذين كان لديهم تخطيط القلب طبيعيا كان لديهم انسداد في الشريان الايسر, 66 مريض من اجمالي 156 و72 في الشريان المحيطي و45 في الشريان الايمن, واما مرضى الحزمة الكهربائية اليسرى كان هناك 18مريض لدية انسداد في الشريان الايسرمن اصل 53, و14مريض لدية انسداد في الشريان المحيطي, و8 مرضى في الشريان الايمن. واما مرضى الحزمة الكهربائية اليمنى كان لديهم 6 مرضى مصابين بانسداد الشريان الايسر من اصل 41 و4 مرضى لديهم انسداد بالشريان المحيطي و6 بالشريان الايمن.في المرضى الذين كان لديهم تخطيط القلب طبيعيا كان لديهم 85 مريض لدية انسداد في شريان واحد و43 لديهم انسداد في شريانيين و17 لديهم انسداد في ثلاث شرايين.واما مرضى الحزمة الكهربائية اليسرى كان لديهم 37 مريض لدية انسداد في شريان واحد و13 مريض في شريانين ومريضان لديهم انسداد في ثلاث شرايين.والحزمة الكهربائية اليمنى 35 مريض لدية انسداد في شريان واحد و4 مرضى لديهم انسداد في شريانيين | Background : Stable angina is one of the manifestation of ischemic heart disease in about 20 to 40 % of patients, The typical patient with angina occurs in a man> 50 years or a women >60 years of age, Findings on the resting electrocardiogram (ECG) are normal in half of patients with chronic stable angina. (1)Aims of the study : To study the coronary angiographic findings in patients with chronic stable angina and normal ECG, LBBB or RBBB.Patients and methods : A cross sectional study conducted in the Iraqi center for heart diseases. In the period from 15 January 2018 to 15 July 2018 which included patients with chronic stable angina and had normal ECG or BBB either LBBB or RBBB. All patients underwent echocardiography, the ejection fraction and contractility of the heart had reported. A special form of questionnaire had been constructed by the researcher to comprise the required data. It include the general information such as : age, gender, as well as smoking habits and history of hypertension and diabetes and history of symptoms of chest pain either typical or atypical. All patients had done coronary angiography and data had been taken from reports, then statistical analysis done. Results : In the present study mean of age of the patients with abnormal coronary angiography was 57.5, most of the patients were male, and most of the patients with DM had abnormal coronary angiography and most of the typical symptoms had abnormal coronary angiography, patients with normal ECG had LAD lesion in 66 patients from total 156 and LCX 72 and RCA 45 and in patients with LBBB 18 had LAD, 14 LCX, 8 had RCA and in RBBB 6 had LAD, 4 had LCX, 6 had RCA, and most of lesion were critical then intermediate and less for subtotal and total.In patients with normal ECG 85 had one vessel 43 had two vessel 17 had three vessel and in LBBB 37 had one vessel 13 had two vessel and 2 had three vessel and in RBBB 35 had one vessel 4 had two vessel.Conclusions1 - The most predominant artery in patients with CSA and normal ECG is LCX then LAD.2 - Most of the lesion in CSA and normal ECG, LBBB, RBBB is critical then intermediate and less subtotal and total.3 - One or two even there vessel disease could occurs in patients with CSA and normal ECG/LBBB, RBBB, but most of the cases are with one then two vessel and less for three vessel.4 - In BBB no specific artery is related to BBB although predominance was for LAD.

سرطان الثدي عند النساء العراقيات من نوع HER2 +VE مع الفائدة من استخدام العقار المناعي Trastuzumzb بعد الانتكاسه السريريه لاستخدامه == Her2 positive Iraqi breast cancer women Use of trastuzumab beyond progression

Author name: وليد جاسم محمد
Supervisor name: منور عبد الاله النقاش
General topic: Medicine
Specific topic: Therapeutic Radiology
Degree: Higher Diploma
Language: English
University location: Baghdad
First pages:
Abstract: Background : Breast cancer is the most frequently diagnosed cancer and the leading cause of cancer death in women. Her 2 positive disease carries worse prognosis and anti her 2 therapy is required in addition to chemotherapy which increase the cost of management of those patients especially in metastatic settingObjectives : The aim of this study to assess Iraqi breast cancer patients with HER2/neu molecular profile. Evaluate the role of using Trastuzumab in metastatic HER2/neu positive breast cancer patients beyond progression after its use in first line by changing the chemotherapeutic agent only.Patients & Methods : This is a retrospective study which was conducted in oncology teaching hospital - medical City complex from 1st of July 2017 to 1st of December 2017, carried out on 253 breast cancer female patients diagnosed within the period 2010 - 2017 with different age groups. Their histopathological reports, immunohistochemistry (IHC) results including ER, PR, HER2/neu and CISH test when indicated in addition to their clinical profile were collected. The subgroup of patients (253) with her2 positive disease were identified. From which patients with metastatic disease were analyzed for the use of trastuzumab beyond progression.Results : The mean age ± SD was (51.7 ± 11.1) years in HER2/neu positive patients, while it was (51.4 ± 13.8) in metastatic HER2/neu patients. The prevalence of HER2/neu positive 16.656 %( 95% CI : 16.468_16.843%). The mean of number of trastuzumab cycles used in patient that not metastatic HER2/neu was (16.6 ±3.9) and at metastatic HER2/neu was (16.1 ± 6.9). Median time to progression was 16 (95% CI : 11.009 - 20.991) months, after 6 months 92.8% had progression - free and after 12 month 53.8% had progression - free.Conclusion : HER2/neu positive disease constitutes 16.656% of Iraqi patients with breast cancer. And the median age for metastasis was (51.4 ± 13.8).Also Trastuzumab use beyond progression had a clinically significant metastatic free survival benefit. The cumulative incidence of metastasis to different body organs was lung (89.8%), liver (57.6%), and bone (45.8%), brain (27.8%).

احداث الشريان التاجي بعد عام واحد من اعادة التوعية تجربة مركز واحدة == Coronary artery events one year after revascularization : a single center experience

Author name: مروان كامل عبود
Supervisor name: حسن يوسف النجار
General topic: Medicine
Specific topic: Diseases - Heart
Degree: Higher Diploma
Language: English
University location: Baghdad
First pages:
Abstract: associated with concerns about their potential adverse effects. In - stent restenosis and stent thrombosis definitely affect the PCI outcome. However, review of recent relevant studies suggests that stent - related problems may have been somewhat overestimated when compared to coronary artery disease (CAD) progression at non stented coronary segments as causative factors of adverse cardiac clinical events late post - PCI.Both stent - related problems and native CAD progression have to be equally addressed to optimize the PCI clinical benefitAim of the study : To study the major adverse cardiac events and one year outcome after PCI.Patients & Methods : This study is cross - sectional study of all patients who were referred to Iraqi Center for heart disease, for further evaluation of suspected coronary artery disease (CAD) for the period January to July 2018. The total number of patients was fifty (50).Results : The total No. of patients were 50, mean age was 59.1±11.3, (22%) were below age 45 and (78%) equal and above age 45 year.54% were male and (46%) were female. The frequency risk factors were DM (62%), HT (56%), Dyslipidemias (52%), Obesity (21%) and Smoking (21%). The most common clinical presentations were chronic stable angina (98%) of cases and one case (2%) acute coronary syndrome. The outcome of PCI after one year divided in to four groups, group A : patients with ISR (5/50) (10 %), group B : patients with new stenosis (8/50) (16 %),group C : patients combined lesions (16/50) (32%) and group D (21/50) (42%) cases were normal.Conclusion : After one year from PCI there was high frequency of recurrence of symptoms exceeding half of the patients, most of them due to development of new lesion.

مستوى فيتامين د والكالسيوم في مصل الدم لدى النساء الحوامل اللواتي يعانين من القئ المفرط الحملي في مستشفى بغداد التعليمي == Serum Vitamin D and Calcium levels in Pregnant Women with Hyperemesis Gravidarum at Baghdad Teaching Hospital

Author name: نور جليل جبار الصائغ
Supervisor name: علياء مكي حسن الصافي
General topic: Medicine
Specific topic: Community Medicine
Degree: Master
Language: English
University location: Baghdad
First pages:
Abstract: الخلفية : نقص فيتامين (د) ومستوى الكالسيوم في الدم له علاقة مع القيء المفرط الحملي. كان هدف الدراسة الحالي هو فحص مستويات فيتامين د والكالسيوم في مصل الدم لدى النساء الحوامل المصابات بالقيء المفرط الحملي وتاثيراته على صحة الانجاب لدى النساء الحوامل.طريقة البحث : هذه دراسة مقطعيه تشمل 97 مشاركة تشمل النساء الحوامل المصابات بالقيء المفرط الحملي تمت في مدينة الطب / بغداد / العراق. تم جمع البيانات من قبل الباحث بعد اعداد استبيان منظم لهذا الغرض بعد الحصول على الموافقة اللفظية من قبل المشمولين بالدراسة (عمر الامهات، الاقامة، الحالات الزوجية، الاقتصادية والاجتماعية، والتعليمية والمهنية، التاريخ الحملي السابق والحالي ومؤشر كتلة الجسم). اجريت التحاليل المختبرية بحساب نسبة فيتامين د والكالسيوم في مصل الدم.النتائج : ان اعمار النساء المشاركات بهذه الدراسة كان يتراوح بين 16 الى 41 عام، حيث ان 70% من المشاركات في هذه الدراسة كان متوسط اعمارهم يتراوح بين 25 الى 35 عام. ان اغلب المشاركات كانوا من متوسطي الدخل المعاشي (40%)، مستوى تعليم متوسط (54%)، ربات البيوت (77%) ونساء متعددات الولادات (1 الى 3 ولادات) (47%). حسب منظمة الصحة العالمية ان معدل الاسقاطات بين النساء للحوامل يمثل نسبة عالية تصل الى (25%) والنساء اللاتي يلدن ولادات ميتة ايضا يشكل نسبة مرتفعة (12%). كان مؤشر كتلة الجسم 56 ٪ من عينة الدراسة. فيما يتعلق بفقر الدم، كان معظم عينات الدراسة يعانين من فقر الدم (70 ٪) مع التاريخ الغذائي السيئ اثناء الحمل (61 ٪) وانخفاض التعرض للشمس (84 ٪). وجود فقر الدم (فيتامين د : ص = 1.0؛ الكالسيوم : ر = 1.0) والتاريخ الغذائي (فيتامين د : ص = 0.07، ع = 0.82؛ كالسيوم : ر = 1.0) اثناء الحمل، كان له ارتباط عالي غير مهم للانقسام من النساء مع نقص فيتامين (د) وانخفاض الكالسيوم في الدم.الاستنتاج : توصلت الدراسة الى ان نسبة عالية من النساء الحوامل اللواتي يعانين من القيء المفرط الحملي تعاني من نقص في فيتامين د ومستوى الكالسيوم في مصل الدم، وكشفت ايضا ان الامهات التي يعنين من نقص فيتامين د ومستوى الكالسيوم في مصل الدم اثناء الحمل واللواتي يعانين من القيء المفرط الحملي يرتبطان ارتباطا بشكل كبير مع ارتفاع خطر الاصابة بفقر الدم. ان خطر نقص في فيتامين د ومستوى الكالسيوم في مصل الدم النساء الحوامل اللواتي يعانين من القيء المفرط الحملي ارتفاع في النساء الحوامل اللواتي كن ربات البيوت وذوي الحالة الاجتماعية والاقتصادية المنخفضة وكذلك الاقل تعرض لاشعة الشمس، ومعدومة النشاط البدني، وكمية اقل من تناول المكملات التي تحتوي على فيتامين د ومكملات الكالسيوم | Background : Vitamin’D’deficiency has a close relation with hyperemesis’gravidarum and serum’calcium level.The current study objective was’to investigate the levels of vitamin D’and serum calcium in pregnant women’with hyperemesis gravedarum and their’effects on their obstetric health. Methodology : This is a’cross - sectional study including 97’pregnant woman with hyperemesis’gravedarum’conducted in’Baghdad Teaching Hospital from the period of seven month starting from November 2017 to May 2018. Data collection from direct interview for the pregnant women.The sociodemographic’data was collected by researcher following a’structured questionnaire about (maternal age, residency, marital, economic and social states, educational and occupation states, previous and current obstetrical history and body mass index were collected). Laboratory Investigations were’done to’estimation of vitamin D and serum calcium level. Results : The age of women included in the study ranged from 16 to 41 years and 70% of them were between 25 and 35 years. Most of the participants were medium socioeconomic state (40%), secondary educational level (54%), homemakers (77%), and multipara (1 - 3 para) (47%). History of miscarriage among pregnant females (23%) and history of fetal death was (12%). Body Mass Index was 56% of study sampl, which are obese women. Regarding the anemia, most of study sampl was anemic (70%) with bad dietary history during pregnancy (61%) and low sun exposure (84%). The presence of anemia (vitamin D : r=1.0; calcium : r=1.0) and dietary history (vitamin D : r=0.07, p= 0.82; calcium : r=1.0) during pregnancy, had non - significant high correlation to division of women with deficient Vitamin D and low serum calcium. Conclusion : The study findings that high percentage in pregnant women with Hyperemesis Gravidarum has deficiency in serum vitamin D and calcium level also revealed that’maternal vitamin D deficiency’and low serum calcium in pregnant women with Hyperemesis Gravedarum are’significantly associated with elevated’risk for anemia. The risk of’vitamin D deficiency and low’serum calcium was higher Hyperemesis Gravedarum pregnant women which were’housewives, and those with low’socioeconomic state and less exposure to’sunlight, no physical activity, and less’vitamin D and calcium supplement intake.

تقويم معدل الاستنبات ومستوى السايتوكينات في المريضات المصابات بالعقم الغير مفسر بعد الخضوع لخدش بطانة الرحم == Evaluation of Implantation Rate and Cytokines Level of unexplained Infertile Patients Undergoing Induced Endometrial Scratching

Author name: ايمان حسن فليح
Supervisor name: عفان عزت حسن | الفت محمد علي النقاش
General topic: Medicine
Specific topic: Obstetrics and Gynecology
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: العقم مشكلة عالمية تؤثر على الملايين من الازواج ،ان اقرب تعريف للعقم هو مرض يصيب الجهاز التناسلي ويؤدي الى الفشل في تحقيق الحمل السريري بعد مرور12 شهرا او اكثر من الجماع الجنسي غير المحمي.وقد اقترحت العديد من الدراسات وجود تاثير ايجابي في خدش بطانة الرحم المقصودة على معدل نجاح انغراس البيضة المخصبة، وخاصة في النساء اللاتي عانوا فشل متكرر او اجهاض متكرر او العقم بدون اسباب مبررة. احداث خدش في بطانة الرحم يعزز رد فعل التهابي وهو مفيد لتفضيل زرع الجنين. يتم تجنيد الخلايا القاتلة الطبيعية والبلاعم والخلايا الشجيرية في الموقع المصاب وكميات متزايدة من السايتوكينات وعوامل النمو والجاذبات الكيمياوية، مثل عامل النخر (TNF - α) وinterleukin - 6 (IL - 6) ، مما يعزز غرس ناجح.صممت الدراسة لتقصي تاثير خدش بطانة الرحم على افراز المصل والبطانة من TNF - α وIL - 6 ، وتاثيره على تعزيز عملية الزرع الناجحة. اجريت الدراسة في مستشفى العلوية التعليمي ومركزمتخصص لعلاج العقم في بغداد. سجلت هذه الدراسة مريضات يعانون من عقم غير مفسر لاكثر من سنة وبعمر اقل من 45 عاما. تم اجراء دراسة هرمونية اساسية ، وتم تقسيم عينة الدراسة كما هو محدد الى ثلاث مجموعات ، 31 (29.5 ٪) على الجماع العفوي الطبيعي ، 31 (29.5 ٪) للتلقيح داخل الرحم (IUI) و43 (41.0 ٪) للتخصيب الاصطناعي) الاخصاب خارج الجسم اوطفل الانبوب) ثم تعريض جميع المريضات الى خدش بطانة الرحم في اليوم 8 من الدورة الشهرية (الدورة التي سبقت دورة الاخصاب خارج الجسم اوطفل الانبوب في مجموعة الاخصاب الاصطناعي او طفل الانبوب) ، عن طريق استخدام الناظور الرحمي ، تم قياس TNF - α وIL - 6 في افرازات المصل والبطانة قبل وبعد الخدش.كانت معدلات الحمل 22 (33.33 ٪) ، 20 (30.30 ٪) ، و24 (36.4 ٪) عن مجموعة الجماع العفوي الطبيعي ، التلقيح داخل الرحم ، والتخصيب الاصطناعي، على التوالي ، وكانت حسابات الاختطار النسبي للحمل اعلى للمجموعة العفوية مع 1.194 RR ، 95٪ CI (0.892 - 1.1601) ، تليها مجموعة التلقيح داخل الرحم مع RR 1.038 ، 95٪ CI (0.757 - 1.423) ، وادنى في مجموعة التلقيح داخل الرحم ، مع RR 0.824 ، وCI 95٪ (0.600 - 1.131).من خلال قياس اثنين من اهم السيتوكينات في افرازات المصل والبطانة من المرضى المشاركين في هذه الدراسة قبل وبعد خدش بطانة الرحم ، وجد انه كان هناك فرق ذو دلالة احصائية (قيمة p <0.001) في TNF المصل والبطانة لانها كانت 3.84 ± 2.41 بيكوغرام / ديسيلتر ، و3.81 ± 2.30 بيكوغرام / ديسيلتر ، على التوالي ، وارتفعت الى 17.35 ± 6.39 بيكوغرام / ديسيلتر في المصل و22.84 ± 9.67 بيكوغرام / ديسيلتر في افرازات بطانة الرحم بعد خدش. كما اظهر IL6 اختلافا معنويا في المصل وفي افرازات بطانة الرحم ، حيث بلغ متوسط مستويات المصل IL6 4.27 ± 2.18 بيكوغرام / ديسيلتر قبل الخدش وارتفع الى 16.46 ± 4.27 بيكوغرام / ديسيلتر بعد الخدش ، في حين كان IL6 في افراز بطانة الرحم 3.86 ± 2.42 بيكوغرام / ديسيلتر قبل الخدش وزيادة الى 22.35 ± 9.14 بيكوغرام / ديسيلتر بعد الخدش.كان تاثير خدش بطانة الرحم على مؤشر النبض ذو دلالة احصائية مع فارق متوسط 0.893 ± 0.393 حيث كان 3.584 ± 0.373 قبل الخدش وانخفض الى 2.690 ± 0.357 بعد الخدش ، مع تغير متوسط النسبة بنسبة 24.54٪ ± 9.95٪.كانت هناك علاقة ارتباط معتدلة ذات دلالة احصائية مهمة بين تطور الحمل وارتفاع مستوى المصل والـ TNF ، وكانت اعلى في افرازات بطانة الرحم من TNF المصل ، ولكن بالنسبة لـ IL6 لم يكن هناك سوى علاقة ضعيفة ذات دلالة احصائية بين بطانة الرحم IL6 والحمل.وخلصت هذه الدراسة الى ان خدش بطانة الرحم يزيد معدل الحمل في جميع مجموعات الدراسة ولكن الحمل العفوي اكثر من التلقيح داخل الرحم، والاخير اكثر من التخصيب الاصطناعي. يسبب خدش بطانة الرحم زيادة كبيرة في تركيزات المصل وافرازات البطانة من TNF - α وIL - 6. وارتبط ارتفاع مستويات TNF - α وIL - 6 مع نتائج حمل افضل. ان خدش بطانة الرحم يقلل من معدل مؤشر المقاومة الشريانية للشريان الرحمي الذي يعني معدل تدفق افضل للدم وبالتالي تحسين نتيجة الحمل. | Infertility is a worldwide problem, affecting millions of couples, and never an old subject. Infertility is “a disease of the reproductive system defined by the failure to achieve a clinical pregnancy after 12 months or more of regular unprotected sexual intercourse. Several studies have suggested a favorable effect of endometrial injury on the implantation success rate, especially in women with recurrent implantation failure or recurrent abortion or unexplained infertility. When local injury - induced in endometrial tissue this enhance an inflammatory reaction which is useful for favors implantation of embryo. Natural killer cells, macrophages, and dendritic cells are recruited to the injured site and increased quantities of cytokines, growth factors, and chemokines like Tumor necrosis factor - alpha, and interleukin - 6, all are secreted, thus resulting in a successful implantation. This prospective interventional study was designed to evaluate the effect of endometrial scratch on serum and endometrial secretion of Tumor necrosis factor - alpha and interleukin - 6, and its effect on promoting successful implantation. The study was done in Al - Alwia Teaching Hospital and privet infertility treatment center in Baghdad from January 2016 till December 2017. This study enrolled 105 female patients with unexplained infertility for more than 1 year and with age under 45 years. Basic hormonal study was done, and study sample was divided as indicated into three groups, 31 (29.5%) for natural conception, 31 (29.5%) for intrauterine insemination and 43 (41.0%) for in vitro fertilization program ,then all patients undergone endometrial scratch, at day 8 of menstrual cycle (in in vitro fertilization program group the scratch of endometrium done in the cycle that preceded the in vitro fertilization procedure ), by using hysteroscopy. Tumor necrosis factor - alpha, and interleukin - 6 was measured in serum and endometrial secretions before and after scratch. pregnancy rates for three groups was 22 (33.33%), 20 (30.30%), and 24 (36.4%) for Natural, Intra Uterine Insemination and In Vitro Fertilization , respectively and when calculate the relative risk (beneficial risk) for pregnancy it reveal that the highest for Natural conception group with 1.194 RR, 95% confidence interval (0.892 - 1.1601), followed by Intra Uterine Insemination group with RR of 1.038, 95% confidence interval (0.757 - 1.423), and lowest in In Vitro Fertilization group, with RR of 0.824, and 95% confidence interval (0.600 - 1.131). By measuring two of the most important cytokines in serum and endometrial secretions of patients involved in this study both before and after endometrial scratch, it was found that there was a highly significant difference (p - value <0.001) in serum and endometrial Tumor necrosis factor - alpha, as were 3.84 ± 2.41 pg/dl, and 3.81 ±2.30 pg/dl, respectively, and increased to 17.35 ±6.39 pg/dl in serum and 22.84 ±9.67 pg/dl in endometrial secretions after scratch. Also interleukin - 6 showed highly significant difference in serum and in endometrial secretions, as the mean serum levels of IL6 was 4.27 ±2.18 pg/dl before scratch and increased to 16.46 ±4.27 pg/dl after scratch, while the interleukin - 6 in endometrial secretion was 3.86 ±2.42 pg/dl before scratch and increased to 22.35 ± 9.14 pg/dl after scratch. The effect of endometrial scratch on pulsatility index was statistically significant with a mean difference of 0.893 ±0.393 as it was 3.584 ± 0.373 before scratch and decreased to 2.690 ± 0.357 after scratch, with mean percent change of 24.54% ± 9.95% reduction. There was a moderate statistically significant positive correlation between developing pregnancy and higher serum and endometrial Tumor necrosis factor - alpha, and that it was higher in endometrial secretions than serum Tumor necrosis factor - alpha , but for interleukin - 6 there was only a weak statistically significant correlation between endometrial interleukin - 6 and pregnancy. This study concluded that endometrial scratch increase pregnancy rate in all study groups but Natural conception is more than Intra Uterine Insemination and Intra Uterine Insemination is more than In vitro Fertilization - Embryo Transfer. Endometrial scratch causes a significant increment in serum and endometrial concentration of Tumor necrosis factor - alpha and IL - 6. Higher levels of Tumor necrosis factor - alpha and interleukin - 6 were associated with better pregnancy outcomes. Endometrial scratch decrease pulsatility index which mean better blood flow rate and good pregnancy outcome.

مجموعة التباين الوراثي احادي القاعدة للتلومريز, XPC وXRCC7 المتغيرة جينيا في المرضى المدخنين العراقيين المصابين بورم المثانة == Single Nucleotide Polymorphism (SNP) Panel for Telomerase, XPC, and XRCC7 Genes Variants in Iraqi Smoker Patients with Bladder Tumor

Author name: صالح علي محمود
Supervisor name: هدف ظافر الياسين | اسامة سليمان الناصري
General topic: Medicine
Specific topic: Clinical Biochemistry
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: سرطان المثانة هو واحد من اكثر الاورام الخبيثة شيوعا في المسالك البولية. يعتبر استهلاك التبغ لفترات طويلة احد العوامل الرئيسية المسببة لتطور سرطان المثانة ، والتي تسبب تلف الحمض النووي. ولذلك ، فان مسار اصلاح الحمض النووي هو من اهم النظم التي تحافظ على سلامة الجينات ومنع التسرطن. وكان الهدف من هذه الدراسة هو معرفة تاثير التباين الوراثي احادي القاعدة لثلاثة جينات مسؤولة عن اصلاح الحمض النووي TEP1 / rs2228041 , XPC / rs2228000) و( XRCC7 7003908 على الخطر بالاصابة بهذا المرض.الاهداف : ان الهدف الرئيسي من هذه الدراسة هو محاولة ايجاد علاقة بين التباين الوراثي احادي القاعدة الموجودة في ثلاثة جينات مختلفة مسؤولة عن اصلاح الحمض النووي والتحقق من تاثير تدخين التبغ على التباين الوراثي الموجود في جنات اصلاح الحمض النووي البشري TEP1 / rs2228041 ) ، XPC / rs2228000 و(XRCC7 7003908 في المرضى الذين يعانون من سرطان المثانة في وتاثيرها على تطور ومرحلة المرض.المرضى وطرق العمل : اشتملت هذه الدراسة على مجموع من 62 مريض مشخص بسرطان المثانة و38 شخص من الاصحاء مطابقين لهم بالعمر والجنس. تم جمع هذه العينات في الفترة من فبراير الى سبتمبر لسنة 2017 في دراسة مقارنة لمجموعه المرضى والاصحاء التي اجريت في قسم الكيمياء الحيوية في كلية الطب بجامعة بغداد.تم الكشف عن النمط الجيني لل TEP1 / rs2228041 (C> T) وXPC rs2228000 (C> T) باستخدام تفاعل البلمرة المتسلسل وطريقة سانجر في ايجاد تسلسل الحمض النووي.بينما كشف عن النمط الجيني للتباين الوراثي XRCC7 (T> G) باستخدام تفاعل البلمرة المتسلسل والمتحدد بطول القطعة المتباينة الشكل, (PCR - RFLP) وتاكيده تسلسل الحمض النووي باستخدام طريقة سانجر. تم حساب نسبة الارجحية (OR) ومجال الثقة 95 ٪ (CI) كمقياس للتاثير المشترك للتدخين السجائر ، والجينات اصلاح الحمض النووي المتباينة الشكل على خطر الاصابة بسرطان المثانة وتطوره ومراحلهه.النتائج : في هذه الدراسة ، اظهر الاليل T المتباين الشكل للجين TEP1 rs222804 علاقة معنوية في زيادة خطر الاصابة بسرطان المثانة (OR = 4.7, *p=0.04). ايضا ، اظهر الاليل T وجود علاقة معنوية في زيادة خطر الاصابة بسرطان المثانة بين الافراد المدخنين (OR =7.02, *p=0.01)علاوة على ذلك ، اظهر الاليل T علاقة معنوية لمرحلة T2 لسرطان المثانة ((OR=13.2, **p=0.001 اظهر النمط الوراثي المغاير الزيجة من XPC rs2228000 (C> T) زيادة كبيرة في خطر الاصابة بسرطان المثانة (OR=2.75, *p value<0.05). كذلك ، قد وجدت الدراسة ان المرضى الذين يعانون من الاليل متعدد الاشكال للنمط الجيني T قد زاد بشكل كبير من خطر الاصابة بسرطان المثانة (OR= 2.7; *p = 0.02).احصائيا, وجدت زيادة معنوية كبيرة في خطر الاصابة بسرطان المثانة عند الاشخاص المدخنين الحاملين للاليل T (OR= 4.3; **p = 0.004).علاوة على ذلك ، لوحظ ايضا ان الطرز الوراثية للاليل T ترتبط بزيادة ملحوظة في خطر T1 (OR= 3.9 **p = 0.005).في الدراسة الحالية ,ان خطر الاصابة بسرطان المثانة قد ازداد بشكل كبير لدى الاشخاص الحاملين للجين متعدد الاشكال متماثل الزيجة الوراثية (للنمط الجيني GG) (OR= 4.0; *p = 0.03) في حين ان النسبة بهذا الخطر قد قلت لدى الاشخاص الذين لديهم جين من النوع الطبيعي (للنمط الجيني TT). ايضا ، زيادة خطر الاصابة بسرطان المثانة زيادة كبيرة احصائيا بين الافراد الحاملين للاليل G(OR= 5.5; ***p = 0.0001). كما لوحظ ان النمط الوراثي للاليل G مرتبط بزيادة كبيرة بخطر الاصابة بالمرحلة T2 لسرطان المثانة (OR= 3.7; **p = 0.001) ، وايضا Ta (OR= 3.5; **p = 0.003).استنتاجتوحي الدراسة الحالية ان وجود الانماط الجينية المتباينة الاشكال لجينات اصلاح الحمض النووري للمروثات يمكن ان يزيد من خطر الاصابة بسرطان المثانة ويؤثر ايضا على تطور ومراحل المرض في حين ان النمط الجيني الطبيعي يمكن ان يقلل من خطر الاصابة بسرطان المثانة وزيادة معدل البقاء على قيد الحياة لمرضى سرطان المثانة. علاوة على ذلك ، يمكن لهذه الاشكال الجينية ان تكون اداة مفيدة لمعالجة المرض للافراد الذين لديهم مقاومة لعلاج السرطان. | XPC Xeroderma pigmentosum CXPG Xeroderma pigmentosum G AbstractBackgroundBladder cancer is one of the most common malignancies of the urinary tract. Prolonged tobacco consumption constitutes the major etiological factors for bladder cancer development, which induce DNA damage. Therefore, DNA repair pathway is a crucial system in maintaining genomic integrity and preventing carcinogenesis. The present work was aimed to predict the consequence of three polymorphisms of the DNA repair genes (TEP1/rs2228041, XPC/rs2228000, and XRCC7 7003908) on the disease predisposition.ObjectivesThe main objective of this study is attempted to find the association between SNPs in different DNA repair pathway and investigating the influence of active tobacco smoking on human DNA repair gene polymorphisms (TEP1/rs2228041, XPC/rs2228000 and XRCC7 7003908) in patients with bladder cancer in and the impact of these polymorphism on the staging and development of the disease.Subjects and MethodsA total of 62 of histo - pathologically confirmed diagnosed bladder cancer patients, and 38 age - matched healthy controls were involved in the study. All were recruited from February to September 2017 in a case - control study conducted at the Department of Biochemistry - College of Medicine University of Baghdad. Genotyping of the TEP1/rs2228041 (C>T) and XPC rs2228000 (C>T) was evaluated using polymerase chain reaction and fully genotyped by Sanger sequencing method. Genotyping of the XRCC7 polymorphism (T>G) was evaluated using a polymerase chain reaction - restricted fragment length polymorphism (PCR - RFLP) and confirmed by Sanger sequencing method. The odds ratio (OR) and 95% confidence interval (CI) were calculated as a measure of the combined effect of cigarette smoking, and DNA Repair Genes Polymorphisms on bladder cancer risk, staging.ResultsIn this study, the polymorphic T allele of the TEP1 rs222804 polymorphism showed a significant association in increase bladder cancer risk OR = 4.7, p=0.04. Also, the T allele showed a significant association in increase bladder cancer risk among smoker individuals OR= 7.02, p=0.01. Furthermore, the T allele showed a significant association for the T2 stage of bladder cancer (OR=13.2, p=0.001). Heterozygous genotype of the XPC rs2228000 (C>T) showed a significant increase in bladder cancer risk OR =2.75, p value<0.05. Also, the study found that patients with the polymorphic allele (T genotype) have significantly increased the risk of bladder cancer (OR= 2.7; p = 0.02). A statistically highly significant increased in bladder cancer risk was found in the smoker individuals who carrying T Allele (OR= 4.3; p = 0.004). Moreover, T Allele genotypes were also observed to be associated with a significantly increased risk of T1 (OR= 3.9; p = 0.005). In the current study, individuals with the homo polymorphic gene (GG genotype) have significantly increased the risk of bladder cancer (OR= 4.0; p = 0.03), while subjects having the homo wild - type gene (TT genotype) could decrease the risk of bladder cancer. Also, a statistically highly significant increased bladder cancer risk in the smoker individuals who carrying G Allele (OR= 5.5; p = 0.0001). G Allele genotypes were also observed to be associated with a significantly increased risk of T2 (OR= 3.7; p = 0.001), and for Ta (OR= 3.5; p = 0.003).ConclusionThe present study suggested that having polymorphic genotypes of DNA repair gene polymorphisms (TEP1/rs2228041, XPC/rs2228000 and XRCC7 7003908) could increase the risk of bladder cancer and also affect the development and staging of the disease while having the wild type genotypes could decrease the risk of bladder cancer and increase the survival rate of bladder cancer patients. Furthermore, these gene polymorphisms could be a useful tool to tackle these emerging problems and is an attractive target for individual anticancer treatment.

اتجاه مرض التهاب السحايا للاطفال دون سن 51 عام في مستشفى حماية الطفل التعليمي ومستشفى الطفل المركزي التعليمي قبل وبعد ادخال اللقاح المستدمية النزلية نوع ب في البرنامج الوطني للقاح الاطفال من 2011 - الى 2014 == Trend of Meningitis in children below 15 years old in Welfare Teaching children Hospital and Central Children Teaching Hospital before and after introduction of Haemophillus influenza type b vaccine From 2011 To 2014

Author name: ميس حسن جاسب
Supervisor name: نادية عزيز ناصر
General topic: Medicine
Specific topic: Family Medicine
Degree: Higher Diploma
Language: English
University location: Baghdad
First pages:
Abstract: Meningitis is serious threat to children health (esp. bacterial) particularly in developing countries. Early diagnosis and management may prevent children from death and serious complication ObjectivesTo determine type of meningitis and characteristic and outcome in children below 15 years old in a period before and after introduction of Haemophillus influenza type b (2011 - 2012 - 2013 - 2013(.Method A retrospective cross sectional study of children below 15 years old diagnosed with acute meningitis who were admitted to welfare children teaching hospital and central children teaching hospital in Baghdad for year : 2011 - 2012 - 2013 - 2014. Statistical analysis done by using SPSS version 23.ResultIn 290 patients, The mean age of children with meningitis was 32.46 month (2.6year). Bacterial meningitis was 25.2%, probable meningitis was 26.6%, and viral meningitis was 45.2%. The most frequent type of bacteria in 73 patient was streptococcal Pneumonia 47.9% followed by Neisseria meningitis 24.7% followed by E coli 9.6% then haemophillus influenza 6.8%. There was significant statistical association between type of meningitis with residence area. Case fatality rate was 4.8%, case fatality rate from bacterial meningitis was 10.9%, case fatality from streptococcal pneumonia was 11.4% and from Neisseria meningitis was 22.2%.Conclusion and recommendation Meningitis is more frequent in age below one year. Streptococcal pneumonia was the most frequent bacterial pathogen. The study recommend more study about misuse antibiotic.

مستوى الكالبروتيكتين بروتين (S - 100) في مصل الدم للمرضى المصابين بالتهاب الفقار المقسط في العراق وعلاقته بالعلاج, نشاط المرض وتنميط.HLA == The Serum Level of Calprotectin (S - 100 protein) in Iraqi Patients with Ankylosing Spondylitis and its Relation with Treatment, Disease Activity and HLA Typing

Author name: خالد محمد عبد الواحد
Supervisor name: جاسم محمد كرحوت | محمد هادي العصامي
General topic: Medicine
Specific topic: Microbiology - Immunology
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: لقد اجريت هذه الدراسة في الفترة ما بين تشرين الاول عام 2016 وتشرين الاول عام 2017 على 90 شخصا تم تشخيص 60 منهم على انهم مصابين بالتهاب الفقار المقسط (مجموعة المرضى) وكان 30 منهم يتناولون العلاج التقليدي (الستيرويد و/او العقاقير السامة للخلايا) الذين كانوا يحضرون للعيادة الخارجية للمفاصل بمستشفى بغداد التعليمي في حين كان هناك 30 مريضا اخرين يتلقون العلاج البيولوجي Inliximab infusion)) وهم يحضرون ردهة العلاج البيولوجي وكان هناك ايضا 30 اخرون من مجموعة الاصحاء. تم جمع عينات الدم من المرضى والاصحاء لتقييم الكالبروتيكتين(Calprotectin) (Matrix(metalloproteinase - 3) في مصل الدم وتم الكشف عنها بواسطة مقايسة الممتز المناعي المرتبط بالانزيم ELISA)). تم قياس hs - CRP بواسطة nephlometer كما تم فحص HLA B - 27 بواسطة التفاعل المتسلسل للبوليميريز في الوقت الحقيقي RT - PCR)). كان مجموع مرضى الدراسة الحالية 60 مريضا، كان متوسط اعمارهم 40.05 ± 8.02 سنة ، وكانت نسبة الذكور سائدة اكثر من الاناث في نسبة (M : F 11 : 1). لقد اوضحت الدراسة الحالية ان مستويات الكالبروتيكتين في المصل كانت اعلى في مجموعة المرضى (89.23 ± 73.97) من مجموعة الاصحاء (54.94 ± 20.51) وكان هذا الفرق ذو دلالة احصائية (P= 0.0148) ، وكان اعلى ايضا في المرضى الذين عولجوا بالعلاج التقليدي مقارنة بالمرضى الذين عولجوا بالعلاج البيولوجي (infliximab infusion) وكان الفرق ذو دلالة احصائية (P = 0.0013) بينما لم يكن هناك فرقا احصائيا بين المرضى الذين كان BASDAI وBASFI < 4.0 وغيرهم من المرضى الذين كان BASDAI و4.0 ≤ BASFI ولا بين المرضى الذين HLA B - 27 ايجابية وغيرها سلبية. لقد كان متوسط مستوى المصل من مركب Metalloproteinase - 3 من المرضى اعلى من مجموعة الاصحاء وكان ذو دلالة احصائية عالية (P= 0.0093)وكان اعلى ايضا في المرضى الذين عولجوا بالعلاج التقليدي ، مقارنة بالمرضى في العلاج البيولوجي (infliximab infusion) والفرق كان ذو دلالة احصائية (P value = 0.0235). وفيما يتعلق باختبار hs - CRP الذي كشف ان متوسط مستوى hs - CRP في المصل للمرضى كان اعلى من مجموعة الاصحاء وكان ذو دلالة احصائية عالية (P= 0.0001) وكان اعلى ايضا في المرضى الذين عولجوا بالعلاج التقليدي ، مقارنة بالمرضى الذين كانوا يتلقون العلاج البيولوجي (infliximab infusion) وكان هذا الفرق ذو دلالة احصائية(P = 0.0235). لقد اظهرت الدراسة الحالية ان HLA B - 27 كان ايجابيا في 34 مريضا (56.7 ٪) ، ولم يكن موجبا في اي شخص من مجموعة الاصحاء وكان هذا الفرق ذو دلالة احصائية عالية (P < 0.0001) وكان هناك فرق كبير من hs - CRP بين مجموعات HLA B - 27 الايجابية والسلبية (P= 0.0437) ولم يتم الكشف عن اختلافات اخرى (ESR ، Calprotectin ، MMP - 3 ، BASDAI ، BASFI) بين مجموعة المرضى HLA B - 27 الايجابية والسلبية. فيما يتعلق بالعلاقة بين ESR وCalprotectin وMMP - 3 وhs - CRP في كلا المجموعتين من المرضى. كان هناك ارتباط مباشر كبير بين hs - CRP وESR (P value = 0.005) ولم يلاحظ اي ارتباط بين المعلمات الاخرى في كلتا المجموعتين من المرضى.لقد اوضحت الدراسة ان الكالبروتيكتين في المصل كان اعلى في مجموعة المرضى من مجموعة الاصحاء وكان اعلى في المرضى الذين يتلقون العلاج التقليدي مقارنة بالمرضى المعالجين بالعلاج البيولوجي ولم تكن هناك علاقة بين مستوى الكالبروتيكتين في المصل ونشاط المرض ولا بوجود HLA B - 27 . | patients were diagnosed as established ankylosing spondylitis patients, thirty (30) patients of them were on conventional treatment (steroid and/or cytotoxic drugs) who were attending the Rheumatology Outpatient Clinic of Baghdad Teaching Hospital, while the other thirty (30) patients were on biological treatment (infliximab infusion) attending biological therapy room and other thirty (30) were apparently healthy control group. Blood samples were collected from patients and controls to assess Serum calprotectin and matrix metalloproteinase - 3 which were detected by enzyme linked immunosorbent assay, the high sensitivity C - Reactive Protein was measured by nephelometer,, wherease Human Leucocyte Antigen B - 27 has been done by real time polymerase chain reaction. Out of 60 patients study group included in the current study, their mean age was 40.05 ± 8.02 years, the males were predominant than females in a ratio (M : F 11 : 1). The current study revealed that serum level of calprotectin is higher in patient group (89.23±73.97) than control group (54.94±20.51) and this difference is statistically significant (P - value =0.0148), and also is higher in patients treated with conventional treatment, than in patients treated with biological treatment (infliximab infusion) and the difference is statistically significant (P - value =0.0013) while the difference is not statistically significant between patients whose Bath Ankylosing Spondylitis Disease Activity Index and Bath Ankylosing Spondylitis Functional Index < 4.0 and other patients whose Bath Ankylosing Spondylitis Disease Activity Index and Bath Ankylosing Spondylitis Functional Index ≥ 4.0 nor between patients whose Human Leucocyte Antigen B - 27 positive and others negative. Mean serum level of matrix metalloproteinase - 3 of patients is higher than control group and is highly statistically significant (P - Value 0.0093) and also higher in patients treated with conventional treatment, than in patients on biological treatment (infliximab infusion) and the difference is statistically significant (P - value =0.0235). Regarding high sensitivity C - Reactive Protein test which revealed that mean serum level of high sensitivity C - Reactive Protein of patient higher than control group and is highly statistically significant (P - Value =0.0001) and also higher in patients treated with conventional treatment, than in patients on biological treatment (infliximab infusion) and this difference is statistically significant (P - value = 0.0235). The current study showed that Human Leucocyte Antigen B - 27 was positive in 34 (56.7 %) patients, and in no subject ( 0 %) from control group and this difference is highly statistically significant (P - Value < 0.0001) and there is a significant difference of high sensitivity C - Reactive Protein between positive and negative Human Leucocyte Antigen B - 27 groups (P - value =0.0437) and no other differences detected of (Erythrocyte Sedimentation Rate, Calprotectin, matrix metalloproteinase - 3, Bath Ankylosing Spondylitis Disease Activity Index, Bath Ankylosing Spondylitis Functional Index) between positive and negative Human Leucocyte Antigen B - 27 patients group. Regarding the correlation between Erythrocyte Sedimentation Rate, Calprotectin, matrix metalloproteinase - 3 and high sensitivity C - Reactive Protein in both patients groups; there is a significant direct correlation between high sensitivity C - Reactive Protein and Erythrocyte Sedimentation Rate (P - value=0.005) and no correlation is observed between the other parameters in both patients groups. The study had showed that serum Calprotectin is higher in patients group than control group and also higher in patients on conventional treatment than in patients on biological treatment, and there is no relation between serum calprotectin level and disease activity nor Human Leucocyte Antigen B - 27 typing

تقييم وظائف البطين الايمن لمرضى العيب الاذيني للقلب قبل وبعد القسطرة العلاجية بواسطة تتبع ضربات القلب == Evaluation of RV functions in ASD patients pre & post transcatheter occlusion by speckle tracking

Author name: فينوس عبد الواحد علوان
Supervisor name: علاء عبد الحسين الانباري
General topic: Medicine
Specific topic: Diseases - Heart
Degree: Higher Diploma
Language: English
University location: Baghdad
Key words:
  • Atrial septal defect
  • Speckle tracking defect
  • Right ventricular function
First pages:
Abstract: Background : The atrial septal defect is a common congenital heart disease. Speckle tracking echocardiography is non - invasive diagnostic technique used in assessment of myocardial function. Aim of study : To evaluate the feasibility and reproducibility of right ventricular 2D Strain assessed by speckle tracking in patients undergoing atrial septal defect transcatheter occlusion compared with conventional markers before and after transcatheter occlusion.Patients and methods : A prospective follow up study conducted in Ibn AL - Bitar Specialized Center for Cardiac Surgery in Baghdad during the period from 1st of July, 2017 to 30th of June, 2018 on sample of 30 patients with atrial septal defect and sample of 30 healthy controls. All patients were investigated with echocardiography and speckle tracking one month before transcatheter occlusion and one month after the transcatheter occlusion.Results : Post transcatheter occlusion, there was a significant decrease in mean right ventricular end diastolic dimension (p<0.001) and a significant decrease in mean of tricuspid annular plain systolic excursion (p<0.001). There was a significant increase in global strain speckle tracking echocardiography mean post transcatheter occlusion (p<0.001). The global strain speckle tracking echocardiography mean was significantly higher among controls and atrial septal defect patients in post occlusion while lower among patients in pre - occlusion (p<0.001) with no significant difference in global strain mean between controls and patients in post occlusion (p=0.1). Conclusions : The speckle tracking echocardiography is a valuable diagnostic technique for evaluation of right ventricular function before and after transcatheter occlusion of atrial septal defect in adults

قياس الفعالية الانزيمية وتحديد الطفرات الجينية لانزيم الثايوبيورين الناقل لمجموع المثيل في عينة من الاطفال العراقيين المصابين بسرطان الدم اللمفاوي الحاد == Thiopurine S - Methyltransferase Phenotype and Genotype in a Sample of Iraqi Children with Acute Lymphoblastic Leukemia

Author name: نوار سمير محمد
Supervisor name: منال كمال رشيد | حسنين حبيب غالي
General topic: Medicine
Specific topic: Clinical Biochemistry
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: Background : The most common childhood cancer is acute lymphoblastic leukemia which is only treated with chemotherapy alone.All modern protocols of acute lymphoblastic leukemia treatment used thiopurine drugs as an essential anti - cancer drug which used for a long period of time. The 6 - Mercaptopurine is an anti - cancer drug widely used for treating acute lymphoblastic leukemia patients. The patients with low Thiopurine S - Methyltransferase enzyme activity is with an increased risk of developing drug toxicity and consequently unsuccessful acute lymphoblastic leukemia outcome and even death.Thiopurine S - Methyltransferase is one of the main enzymes involved in 6 - mercaptopurine metabolism, and the low activity of this enzyme is strongly correlated to the Thiopurine S - Methyltransferase genetic polymorphism.Aim : Find out the three most common Thiopurine S - Methyltransferase enzyme polymorphism TPMT*3A, TPMT*3B and TPMT*3C in Iraqi pediatric patients with acute lymphoblastic leukemia, and its frequencies. Analyses of Thiopurine S - Methyltransferase activity in the serum of those patients, and compare the results with other population. Methods : This is a cross - sectional study included eighty - one (81) Iraqi pediatric patients with acute lymphoblastic leukemia during the maintenance phase of their UKALL protocol treatment, receiving 6 - Mercaptopurine drug with age range from 1.83 (1year and 10 months) to 16.25 (16 years and 3 months). Thiopurine S - Methyltransferase activity was measured in the patients’ serum by Enzyme - Linked Immunosorbent Assay technique and three of Thiopurine SMethyltransferase genetic polymorphisms were detected by allelespecific multiplex - PCR analysis after DNA extraction from the whole blood. Liver Function Tests were measured by calorimetric method; Alanine Aminotransferase, Aspartate Aminotransferase, Alkaline Phosphatase and Total Serum Bilirubin in addition to Complete BloodCount measured by automated hematology system. Results : There was significant difference in the mean of Thiopurine S - Methyltransferase activity between pediatric patients carrying the wild - type allele TPMT*1 (n=49), with allele frequencies of 60.4% and pediatric patients (n=32) carrying the mutant alleles (TPMT*3A or TPMT*3C) with allele frequencies of 81.2% and 18.7% respectively. The TPMT*3B allele was not detected in this group. The P - value was highly significant (P<0.000**).Conclusion : This study is the first to analyze Thiopurine SMethyltransferase mutant gene frequency in a sample of the Iraqi population, and it revealed the presence of TPMT*3A and TPMT*3C genetic polymorphism but not a TPMT*3B mutant allele. Thiopurine S - Methyltransferase activity was low in the patients with mutant gene as compared with the wild - type allele patients. Finally, genotype and phenotype of Thiopurine S - Methyltransferase enzyme is an essential predictor to reduce the cytotoxic effects of the anticancer drug and successful acute lymphoblastic leukemia treatment.

تركيزات البلازما والاداة المساعدة للتشخيص لعامل النمو البطاني الوعائي (VEGF) ، مصفوفة ميتالوبروتيناز - 2 (MMP - 2) ، مثبطات الانسجة لمركب الميتالوبروتيناز - 2 (TIMP - 2) والمستعمرة الضخمة (M - CSF) في النساء اللواتي يعانين من ورم الثدي : دراسة مقارنة مع م == Plasma Concentrations and Diagnostic Utility of Vascular Endothelial Growth Factor (VEGF), Matrix Metalloproteinase - 2 (MMP - 2), Tissue Inhibitors of Metalloproteinase - 2 (TIMP - 2), and Macrophage Colony Stimulating Factor (M - CSF) in Women with Brea

Author name: اسيل نبيل كامل
Supervisor name: باسل عويد محمد صالح | كفاح حمدان
General topic: Medicine
Specific topic: Clinical Biochemistry
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: سرطان الثدي هو الورم الخبيث الاكثر شيوعا في النساءويعتبرالسبب الرئيسي الثاني لوفاة مرضى السرطان في العالم. تعتبر الوقاية والكشف المبكر هوالطريقة الاكثر فعالية لمكافحة السرطان. خلال العقد الماضي ، جذبت الكثير من علامات البيوكيميائية لسرطان الثدي انتباه العديد من الباحثين. هذه العلامات يمكن استخدامها في مراقبة العلاج ، والتنبؤ بدرجة اصابة الانسجة ، وسلوك الورم ، ومدى انتشاره ، واحتمالية اصابةالعقد الليمفاوية. من بين هذه الواصمات الحيوية ، عامل نمو بطانة الاوعية الدموية (VEGF) ، خلايا البلعوم المحفزة للحفظ (M - CSF)، ومصفوفة الميتالوبروتنيز MMP - 2))، ومثبطات الانسجة لمركب الميتالوبروتينيز(TIMP - 2). تشير الدلائل المتزايدة الى ان قياس VEGF هو افضل مرشح لتشخيص سرطان الثدي (افضل من مستضد السرطانCA 15 - 3 ) خاصة في المرحلتين الاولى والثانية وكذلك في التمايز بين الورم الخبيث وورم الثدي الحميد. اظهرت الدراسات ان قياس VEGF لا سيما مع CA 15 - 3 ، اعلى فائدة وقوة تشخيصية في الكشف عن سرطان الثدي.وفي الاونة الاخيرة ، تم التوصل في البحوث الحديثة الى ان TIMP - 2 قد يكون ذو فائدة في التشخيص المبكر لسرطان الثدي في مراحله الاولى زتهدف هذه الدراسة الى : 1) قياس تركيزات البلازما لبعض المرقمات الحيوية الجديدة بما في ذلك : عامل نمو بطانة الاوعية الدموية (VEGF) ، ومصفوفة الميتالوبروتينيز ((MMP - 2 ، ومثبط الانسجة لمركب الميتالوبروتينيز ((TIMP - 2 ، وعامل تحفيز مستعمرة البلعم (M - CSF) بالاضافة الى مثبط السرطان 15 - 3 ( CA15 - 3) في النساء المرضى الذين يعانون من ورم الثدي بالمقارنة مع النساء الاصحاء.2) التحقيق في الاداة التشخيصية لكل من المرقم الحيوي المقاس (وبالاقتران مع بعضها البعض) في الكشف عن ورم الثدي و(3) مقارنة النتائج مع معلمات الهستوباثولوجي ( العمر, الجنس , الحالة الزوجية , سن الياس حجم الورم , مرحلة الورم السرطاني , مستقبل الاستروجين , مستقبل الروجيستيرون ومستقبلات 2 Her)المواد وطرق العمل : اشتملت الدراسة على 88 امراة عراقية تم تقسيمهم الى ثلاثة مجاميع : 38 امراة مصابة بسرطان الثدي (Group I, BC) ، 25 امراة مصابات بورم الثدي الحميد الغدي الليفي Fibroadenoma (FA) (Group II, FA benign ) اللواتي تم تشخيصهن من قبل مجموعة اخصائي الاورام و25 امراة سليمة (كمجموعة ضابطة). تم تشخيص ورم الثدي من قبل مجموعة من الاخصائيين في الاورام. حيث تم التشخيص بناء فحوصات تجرى على عينة تؤخذ من خزعة نسيجية من ورم الثدي او بعد استئصال الثدي. تم تنفيذ اجراءات التدريج العلاجي على اساس فحوصات الجسم والدم ، والتصوير الشعاعي للثدي ، وفحص الثدي بالموجات فوق الصوتية ، والاشعة السينية للصدر حسب توفرها وضرورتها. تم اجراء تصنيف الاورام وتدريجها اعتمادا على معايير الاتحاد الدولي لمكافحة سرطان الاورام - (UICC - TNM) واللجنة الامريكية المشتركة لمرحلة مكافحة السرطان. تم تقسيم النساء المصابات بسرطان الثدي الى مجموعات فرعية على اساس مراحل السرطان ؛ المجموعة (ا) : تشمل 12 امراة في المرحلة الاولى (T1N0M0) ، حيث حجم الورم <2 سم ، المجموعة ب : 14 امراة في المرحلة الثانية (T2N0M0 ، T2N1M0 ، T3N0M0) ، حجم الورم (2 - 5) سم ومجموعة C : تشمل 12 امراة في المرحلة الثالثة (T2N2M0 ، T3N1M0 ، T3N2M0 وT4N2M0) ، كما كان لديهم حجم الورم > 5 سم. في هذه الدراسة تم استبعاد النساء المصابات بسرطان الثدي في المرحلة المتقدمة (المرحلة الرابعة) ، والنساء اللواتي يعانين من المرض سابقا او اللواتي يعانين من انواع اخرى من السرطانات؛ السرطانات التناسلية الانثوية (سرطان المبيض ، سرطان عنق الرحم ، سرطان الرحم) ، اورام الكلى ، القولون والمستقيم ، البنكرياس ، الرئة والراس والعنق. ايضا ، تم استبعاد المدخنين والنساء اللواتي يتناولن المشروبات الكحولية من هذه الدراسة. تم سحب عينة الدم من كل امراة لقياس VEGF ، M - CSF ،TIMP - 2,MMP - 2 و3 CA15 - . ايضا تم قياس مصل 25 هيدروكسي فيتامين D (25OHD) ومعلمات الدهون بما في ذلك الكولسترول الكلي (TC) ، والدهون الثلاثية (TG) ، والكوليسترول الدهني عالي الكثافة (HDL - C) ، والكولسترول الدهني منخفض الكثافة (LDL - C) فقط في المجموعة الاولى والمجموعة الثانية | Breast cancer (BC) is the most common malignancy in women and the second leading cause of their death from cancer in the world. The most effective way to combat cancer is its prevention and early detection. During the last decade, biochemical markers of breast cancer have attracted the attention of many researchers. Among these biomarkers, the interest points to Vascular Endothelial Growth Factor (VEGF), Macrophage Colony Stimulating Factor (M - CSF), Matrix Metalloproteinase - 2 (MMP - 2), Tissue Inhibitors of Metalloproteinase - 2 (TIMP - 2). Growing evidence indicates that measurement of VEGF maybe the best candidate for BC diagnosis (better than CA 15 - 3) especially in stages I and II as well as in the differentiation between BC and benign breast tumor. More recently it has been reported that TIMP - 2 maybe useful in early diagnosis of BC and differentiation of breast cancer stages. The aim of this study are to : (1) Measure the plasma concentrations of some of new biomarkers including : Vascular Endothelial Growth Factor (VEGF), Matrix Metalloproteinase - 2 (MMP - 2), Tissue Inhibitor of Metalloproteinase - 2 (TIMP - 2) and Macrophage - Colony Stimulating Factor (M - CSF) in addition to CA 15 - 3 in women patients with breast tumor in compare son with healthy control women, (2) Investigate the diagnostic utility of each of the measured biomarker (and in combination with each other) in detection of breast tumor and (3) Correlate the findings with the clinicopathological parameters (age, menopause, marital status, stages, tumor size, Estrogen Receptor (ER), Progesterone Receptor (PR) and Her - 2/neu receptor) in those patients.Subjects and Methods : Eighty - eight Iraqi women were enrolled in the study; 38 women with primary breast cancer (BC, Group I), 25 women with Fibroadenoma (FA) benign breast tumor (FA, Group II) and 25 apparently healthy women (served as control group). The diagnosis of breast tumor was achieved by the Oncology group. Histopathology investigations were performed by Consultant Histopathologic based on tissue biopsy of mammary tumor or after mastectomy. Tumor classification and staging were performed depending on criteria of International Union against Cancer Tumor - Node - Metastasis (UICC - TNM) classification and the American Joint Committee on Cancer Staging. Accordingly, women with breast cancer were classified into subgroups based on the stage of their BC; Group A : 12 women with stage I, Group B : 14 women with stage II, and Group C : 12 women with stage III. Exclusion criterion includes those women with breast cancer of advanced stage (stage IV), a previous history of multiple type of cancers; female reproductive tract cancers (ovarian, cervical and endometrial cancers), renal, colorectal, pancreatic, lung, head and neck tumors. Blood sample was aspirated from each woman for the measurement of plasma VEGF, M - CSF, MMP - 2, TIMP - 2 and serum CA15 - 3 by using enzyme linked immunosorbent assay (ELISA). Also, serum vitamin D3 was measured in group I only using ELISA and serum lipid profile parameters were measured in group I and group II. Results : The mean (±SD) values of plasma levels of VEGF (p<0.001), MMP - 2 (p< 0.001), TIMP - 2 (p < 0.001), M - CSF (p < 0.05), and CA 15 - 3 (p<0.001) of group I was significantly higher compared to that of group II and controls. However, the mean value of plasma MMP - 2 was the only measured biochemical marker which was significantly increased in group II compared to controls (p<0.001). Regarding the BC stages, the mean values of all the measured biochemical markers were significantly higher in stage III than in stage I and stage II (p<0.001). Interestingly, the mean (± SD) value of plasma TIMP - 2 levels was the only biochemical marker of the measured ones which was significantly increased in stage II than in stage I (p=0.001). The cut - point value of plasma VEGF (>55.73 pg/ml) or TIMP - 2 (>102 ng/ml) (for both, AUC=1.0) was the excellent test in differentiating women with stage I of BC from healthy women. While that of VEGF (>55.73 pg/ml), TIMP - 2 (>102 pg/ml) or CA15 - 3 (>10.82 u/ml) (for all, AUC=1.0) was considered as the best test in discriminating the BC stage II from healthy women. While, the cut - point value of plasma TIMP - 2 (>142 ng/ml) which has the highest (AUC=1.0) considered as the excellent test in differentiating BC stage I from women with fibroadenoma benign tumor (FA). While that of VEGF (>88.67 pg/ml) or TIMP - 2 (>254 ng/ml) which has the highest (for each, AUC=0.991) was considered as the best test in discriminating the BC stage II from FA. In addition, the plasma measurement of VEGF has the superior diagnostic utility in differentiation of FA women and healthy control women (p<0.001, AUC=0.998).Conclusion : Measurement of plasma VEGF (cutoff >55.22pg/ml) or TIMP - 2 (cutoff >102 ng/ml) is the best biochemical marker in diagnosis of stage I or stage II BC and differentiates them from healthy women; they have more diagnostic utility than CA 15 - 3. Also, measurement of TIMP (cutoff > 142 ng/ml) has the excellent diagnostic utility in diagnosis and differentiation of stage I BC from benign tumor fibroadenoma (FA). Moreover, TIMP - 2 (cutoff > 254 ng/ml) or VEGF (cutoff > 88.67 pg/ml) has the superior diagnostic utility over that of CA 15 - 3 in diagnosis and differentiation of stage II BC from FA. Plasma measurement of TIMP - 2 was the best biochemical marker in studying early progression of BC; it can differentiate stage II from stage I BC. Furthermore, plasma measurement of VEGF was found to be the excellent parameter in differentiation between women with FA from healthy ones.

دراسة الوظائف الانقباضية والارتخائية للبطينين الايون والايسر لدى مرض ارتفاع ضغط الدم بواسطة التصوير بالدوبلر النسيجي لصدى القلب == Right Ventricular versus Left Ventricular Systolic and Diastolic Parameters using Tissue Doppler Echocardiography in Hypertensive patients

Author name: مصطفى عبد الامير حسين زاهد
Supervisor name: حسن علي الفرحان
General topic: Medicine
Specific topic: Echocardiography
Degree: Higher Diploma
Language: English
University location: Baghdad
First pages:
Abstract: Background : Hypertension is a heterogeneous disorder with a number of well defined as well as putative etiologies. It is a major risk factor for stroke and cardiovascular diseases, and is thus associated with significant morbidity and mortality.Arterial systemic hypertension may determine impairment of both left ventricular diastolic and systolic function, due to increased afterload but also to changes of left ventricular geometry and structure producing left ventricular remodelling and hypertrophy.Also the right ventricle might be involved in this process by structural and functional abnormalities. Right ventricular chamber diastolic dysfunction has been shown in uncomplicated arterial hypertension [30, 41, 42, 43]. To date, little information is available about functional changes of right ventricular walls in arterial systemic hypertension. This issue is crucial to better understanding of the mechanisms underlying right ventricular involvement in the hypertensive heart. Pulsed tissue Doppler has been used to analyze myocardial left ventricular wall motion abnormalities in several cardiac pathologies [45 - 50] and also appears suitable for assessing changes of right ventricular longitudinal function due to arterial hypertension.Aims : This study evaluates Right & Left ventricular functional and morphological changes in treated hypertensive patients using selected conventional and Tissue Doppler Echocardiographic methods, and Studies the relationship between changes in both Right & Left Ventricles of heart. Finally to determine the relationship between onset of disease and echocardiographic changes.Methods and Results : We selected one hundred and two treated hypertensive patients and 100 healthy age - and gender - matched controls, both study groups underwent echocardiographic examination using 2D, M Mode, Pulsed Doppler and Tissue Doppler imaging.Examination involved left ventricular septal and posterior wall thicknesses, internal dimensions, left atrial area, ejection fraction and LV mass, also Tissue Doppler derived waves' velocities S' , e', a' and e'\a' ratio. Right ventricular internal basal diastolic dimension, free wall thickness in diastole, right atrial area, TAPSE, PASP, fractional area change(FAC), PW tricuspid inflow waves' velocities e, a, and e\a ratio, Tissue Doppler derived myocardial performance index (MPI), S', e', a', and e'\a' ratio.Hypertensive patients had Higher than controls in : Left Ventricular walls' thicknesses, end diastolic dimension, LV mass, left atrial area, peak velocity S', a', Right Ventricular free wall thickness, Tricuspid inflow TV a wave velocity, right atrial area, PASP, TDI S' and a' waves velocities.Lower Values than controls in Left Ventricular TDI peak velocity of e' wave and e'\a' ratio, Right ventricular Tricuspid inflow PW e wave velocity, e\a ratio, internal diastolic dimension, TDI e' and e'\a' ratio.The systolic function of both ventricles was not reduced.The diastolic function of both left and right ventricles were impaired, the Tissue Doppler derived e'\a' ratios were strongly correlated in both ventricles.There was a strong correlation between LVH and both Tissue Doppler derived RV & LV diastolic dysfunction.By studying correlation of echocardiographic finding with disease duration there was a strong relationship with both LVH and RV tissue Doppler diastolic dysfunction.Conclusion : Systemic arterial hypertension causes morphological and functional changes in both ventricles, initially systolic function of LV and RV are not affected; diastolic dysfunction in LV is considered as one of the earliest functional changes, studying RV revealed diastolic dysfunction which was strongly correlated with LV diastolic dysfunction by using Tissue Doppler imaging, also with LVH were highly correlated with disease duration.

تفاعل انزيم البلمرة المتسلسل النسخي العكسي ذي الوقت الواقعي كاداة تشخيصية جزيئية في التحري عن الجينات المدمجة الشائعة في عينة من الاطفال العراقيين المصابين بابيضاض الدم اللمفاوي الحاد == Real time reverse transcriptase polymerase chain reaction as diagnostic molecular tool in screening of common fusion genes in sample of Iraqi children with acute lymphoblastic leukemia

Author name: اريج عماد كاظم
Supervisor name: بان عباس عبد المجيد | سلمى عباس الحداد
General topic: Medicine
Specific topic: Diseases - Blood
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: ابيضاض الدم الليمفاوي الحاد عند الاطفال هو مرض متنوع له اصناف وراثية متعددة تستجيب بصورة مختلفة للعلاج الكيميائي. توجد الكثير من التغايرات الكروموسومية المؤدية الى انتاج جينات مدمجة مصاحبة لحدوث هذا المرض.اهداف الدراسة : لدراسة تعبير الجينات المدمجة الشائعة في ابيضاض الدم اللمفاوي الحاد عند الاطفال باستخدام تقنية تفاعل البلمرة المتسلسل ذي الزمن الواقعي وربط نتائج هذه الدراسة مع مختلف المؤشرات السريرية والمختبرية ثم تقييم هذا التعبير بعد العلاج الاولي.المرضى, المواد وطرق العمل : اجريت هذه الدراسة المستقبلية للحالات والشواهد باستخدام تقنية تفاعل البلمرة المتسلسل ذي الزمن الواقعي لدراسة تعبير الجينات المدمجة MLL - AF4 ,BCR - ABL1 ,E2A - PBX1 ,TEL - AML1 وSIL - TAL1 في ناضح نقي العظم ل 48 مريض بابيضاض الدم اللمفاوي الحاد قبل العلاج مع 46 شخوص ضابطة, تم جمعها من مستشفى حماية الطفل التعليمي / دائرة مدينة الطب للفترة من 1 تموز 2013 الى 31 حزيران 2014. استعمل جين GAPDH كجين مراقب داخلي لدراسة تعبير الجينات المذكورة بعد العلاج.النتائج : من اصل 48 مريض بابيضاض الدم اللمفاوي الحاد, كان هناك 21 ذكرا" و27 انثى مع نسبة ذكور الى الاناث 0.78 : 1 . تراوحت اعمارهم بين 2 شهر الى 13 عام مع متوسط عمر 5 اعوام . تراوحت اعمار 26 مريضا" بين 1 - 5 سنوات. اظهر الفحص الجزيئي الكشف عن نسخ الجينات المدمجة TEL - AML1، E2A - PBX1 وp190 1BCR - ABL في 20.8%, 16.7% و2.1% من المرضى، على التوالي، بينما لم يتم الكشف عن نسخ p210 1BCR - ABL ، MLL - AF4 وSIL - TAL1. بالاضافة الى ذلك، اظهر احد المرضى تعبير نسخي لكل من TEL - AML1 وE2A - PBX1 في الوقت نفسه. وجدت التعابير الجينية بعد بدء العلاج في 2 مرضى من اصل 12 مريض.الاستنتاجات : ان تقنية تفاعل البلمرة المتسلسل ذي الزمن الواقعي طريقة جزيئية دقيقة وقابلة للتطبيق في تصنيف ابيضاض الدم اللمفاوي الحاد في الاطفال. ان نتائج التصنيف الجزيئي للاطفال العراقيين المصابين بابيضاض الدم اللمفاوي الحاد مشابهة نوعا" ما للتقارير العالمية جاعلة TEL - AML1 الجين المدمج الاكثر انتشارا". | Pediatric acute lymphoblastic leukemia is a heterogeneous disease with various genetic subtypes that respond differently to treatment. Many chromosomal aberrations with resultant fusion genes are known to be associated with the disease.Objectives : To study the expression of common fusion genes in pediatric acute lymphoblastic leukemia using a quantitative real time polymerase chain reaction technique, correlate results with different clinical and laboratory findings and evaluate these expressions after initial treatment.Subjects, materials and methods : A case - control prospective study was conducted using qPCR technique to study the expression of TEL - AML1, E2A - PBX1, BCR - ABL1, MLL - AF4 and SIL - TAL1 fusion genes in bone marrow aspirates of 48 untreated acute lymphoblastic leukemia pediatric patients and 46 control subjects, were recruited at the Children Welfare teaching hospital / Medical City directorate for the period from 1st of July 2013 to 31st of June 2014. Post - induction transcripts’ evaluation for 12 ALL patients was done by comparative quantification method using GAPDH as a reference gene.Results : Out of 48 acute lymphoblastic leukemia patients, 21 were males and 27 were females with a male to female ratio of 0.78 : 1. Age ranged from (2 months to 13 years) with 26 patients aged between 1 - 5 years whereas the median age was 5 years. The mean age was 5.9 years + standard error of 0.51 years. Molecular screening demonstrated detection of TEL - AML1, E2A - PBX1 and BCR - ABL1 p190 transcripts in 20.8%, 16.7% and 2.1% of patients, respectively. BCR - ABL1 p210, MLL - AF4 and SIL - TAL1 transcripts were not expressed. One patient expressed both TEL - AML1 and E2A - PBX1 transcripts. Post induction transcripts were detected in 2 out of 12 patients.Conclusions : Real time PCR technique is an applicable molecular method in classifying and predicting prognosis in pediatric ALL. The molecular classification of Iraqi children with ALL is mostly similar to reports worldwide making TEL - AML1 fusion gene the most prevalent type

الاهمية السريرية لدراسة كهروفسلجـة القلب لدى مرضى التسارع الاذيني الانتيابي حول العقدة الاذينية البطينية == CLINICAL IMPORTANCE OF CARDIAC ELECTROPHYSIOLOGICAL STUDY IN PATEINTS WITH ATRIOVENTRICULAR NODAL REENTRANT TACHYCARDIA

Author name: امـين عبد الحسن مانع العـلواني
General topic: Medicine
Specific topic: Diseases - Heart
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: تعتبردراسة كهروفسلجة القلب من الفحوصات القسطارية الضرورية لدى المرضى المصابيين بالتسارع الاذيني الانتيابي والذي يحدث بسسب ظاهرة عودة الدخول الكهربائي حول العقده الاذينية البطينية. تهدف هذه الدراسة الى معرفة الاهمية السريرية لكهروفسلجة القلب في تقييم مرضى التسارع الاذيني الانتيابي حول العقده الاذينيه . لقد خضعوا جميع المرضى الى اجراء قسطرة كهربائية القلب وخلال هذه العملية تتم دراسة كهروفسلجة القلب حيث تم مراقبة التوصيل الكهربائي بين حزمة هز والبطينين وتثبيت سرعة التيار الكهربائي بين الاذين والبطين اثناء التسارع الانتيابي. وشملت هذه الدراسةتسعة وثلاثون مريض من كلا الجنسين وباعمار مختلفة. ومن خلال دراسة كهروفسلجة القلب لديهم تم تقسيمهم الى مجموعتيين المجموعه النموذجية الاكثر انتشارا حسب قياسات المسافة بين البطين والاذين اثناء التسارع الاذيني الانتيابي والتي تكون اقل من 60 مل/ثانيه. وكان عددهم ثلاثة وثلاثون مريض. والمجوعة الثانية وهي اللانموذجية والاقل شيوعا وكان عددهم ستة مرضى. والمسافة بين البطين والاذين اثناء التسارع الانتيابي اكثر من 60 مل/الثانيه. اظهرت النتائج الى ان اكثر من نصف المرضى تكون العقده الاذينيه الحبيبه ذات فيزيولجية ثنائية الذراع (البطيئ والسريع) 62% وهو الغالب في العادة، ولكن من خلال هذه الدراسة وجدت نسبة تكاد تكون عالية 38% نسبيا بين هولاء المرضى حيث كانت العقدة الاذينية البطينية ثلاثية او رباعية الذراع حيث يشترك اكثر من ذراع بطيئ في التسارع الانتيابي. بعد الاعتماد على نتائج الدراسة وتحديد نوع التسارع الاذيني الانتيابي يتم كوي الحزمه الكهربائية في الذراع البطيئ بعد تحديد مكان الذراع بالاعتماد على التشريح والموقع اثناء الدراسة. مع الاخذ بنظر الاعتبار ان جميع المرضى تم كوي الذراع لهم وبشكل ناجح ولكن القسم الاكبر 59% تم قطع الذراع بشكل تام حيث لاثوجد اي اشارات لكهروفسلجة القلب بعد الكوي والقسم الاخر تم كوي الذراع بشكل غير كامل او تغير في التركيب التشريحي للذراع وكانوا 41% من المرضى بالاعتماد على وجود بعض المواصفات من البداية من دون رجوع التسارع الاذيني الانتيابي بعد الكوي خلال تحفيز القلب بعد الكوي. وتم الاستنتاج من خلال الدراسة ان النساء يعانون بنسبة اكبر من تسارع فوق الاذيني المنتظم مقارنة بالرجال. مع وجود نسبة ليست بالقليلة والتي تصل الى ثمانية وثلاثون بالمئة من المرضى تكون فيها فزيولوجية العقده الاذينيه ثلاثية او رباعية الذراع مقارنة بالفيزيولوجية ثنائية الذراع وهو الشائع بالعادة. | AV nodal reentrant tachycardia (AVNRT) considered as the most common regular supraventricular arrhythmia in humans. It originates from a location within the heart above the bundle of His. It is more common in women than men. It represents an important cause of palpitations and to lesser extent, dizzy spells and syncope. An invasive electrophysiological study is a helpful procedure in the classification of AVNRT into common (typical) and uncommon (atypical) types. This study aims to : (1) Assess the role of electrophysiological study in the classification of AVNRT. (2) Explore the presence of multiple pathways in respect to the usual dual AV nodal pathways. And (3) Used EP study as predictor for successful ablation of the slow pathway. This study was conducted on Thirty nine (39) patients of either sex with paroxysmal supraventricular tachycardia corresponding to an AVNRT referred for catheter ablation. Each subject was submitted for history taking, examination, ECG, Echo study and basic invasive cardiac electrophysiological procedure that include right - sided cardiac catheterization through the femoral veins and programmed pacing was performed after localization of the catheters in the heart using the standard stimulation protocol to induce the tachycardia. In addition, His bundle study which involve measurement of atrial - His (AH) interval, Ventricular - atrial time (VA) as a baseline and after tachycardia induction, demonstration of the AH jump and/or echo beat (ectopic) pre and post ablation of the slow pathway using radiofrequency energy. However this study was conducted in Leipzig Heart Center/Germany from January 2013 to February 2014. The result of this study reveals that 33 (84.6%) of the patients developed typical AVNRT and 6 (15.4%) with atypical AVNRT. 25 patients (64.1%) were females (23 (92%) typical type and 2 (8%) atypical type) and 14 patients (35.9%) were males (10 (71.4%) typical type and 4 (28.6%) atypical type). Among the patients group with typical AVNRT the 91.7% discovered to have two AV nodal pathways and 84.6% with three pathways in respect to 8.3% with two AV nodal pathway and 15.4% with three pathways within the patients group with atypical AVNRT. Accordingly, 38.5% of all patients in this study discovered to have multiple pathways. Concerning ablation and modification of the slow pathway, complete ablation is achieved in 59% while modification of the pathways was noticed in 41%. In conclusion, this study concludes that an invasive electrophysiological study is a safe and reliable method for identification of patients with high risk of tachyarrhythmias. Moreover, most of the female patients discovered to have typical AVNRT. Unusually, higher percent of patients developed multiple pathways (more than two pathways) with respect to the usual dual pathways. The disappearance of post ablation EP data (AH jump and/or echo beat) reflect successful complete slow pathways ablation whereas the appearance of these data considered being a modification of the slow pathway

الدور الحتمل لكشف المستضد كالتومانان في مجال التشخيص المختبري من الرشاشيات الهوائية في مرضى نقص المانعة == The possible role of galactomannan antigen detection in laboratory diagnosis of invasive Aspergillosis in immunocompromised patients

Author name: رواء علي محمد
Supervisor name: وفاق محمود الوتار | علي محمد جواد
General topic: Medicine
Specific topic: Microbiology
Degree: Master
Language: English
University location: Baghdad
First pages:
Abstract: This study was conducted to detect the invasive aspergillosis inimmunocompromised patients with rapid diagnostic method (ELISA).This study was conducted on 50 immunocompromised patients, theywere the attendants of Hematology / Oncology Department of BaghdadTeaching Hospital, pediatric oncology wards. The patients presented withfever which is not responding to antibiotics along with cough and sputumand abnormality on chest x - ray . And 11 healthy Iraqi individuals wereincluded in this study. from March 2013 till October 2013.Sputum and serum. initially direct microscopical examination donefor each sample and stained with gram stain. Sputum was immediatelycultured on Sabouraud dextrose agar (SAB) and Brain heart infusion agar(BHI) labeled with same code number of that sputum. Wet preparationwas down from colonies on Sabouraud dextrose agar plate or Brain heartinfution agar for isolation and identification of species of growingmould.This study showed that female to male ratio among patients studygroup was (1.2 : 1) .The age of the patients ranged from from 2 to 70 years with a meanage (31.8 ± 0.8) years. For the control the age ranged from 11 to 60 yearswith a mean age (31.1 ± 0.1) years. The peak mean age group (10 - 20)years with (5.1 ± 0.1).This study showed that 33( 66%) of patients were havingneutropenia which it is highly significant = 11.58 when the P value(P<0.01) , 10 ( 20% ) of patients were having neutrophilia and 7 (14%)of patients were having normal blood film results.IIThis study showed that sputum culture for Aspergillus positive in 18cases and it was negative in 17 patients, it was not done in 15 casesbecause some are from patients were sputum sampling was difficult to beobtained (pediatric), or have no sputum . And the Aspergillus speciesisolated from this culture showed that Aspergillus fumigatus is the most common species isolated from sputum culture 11 (61.1%) of positive culture results.The results showed high significant of AML diseases which composed 18 of 50 (36%) of patients , and most of the patients 24 of 50 (48%) of patients were on amphotericin B treatment.The results of the detection of galactomannan antigen detected by ELISA showed that the difference between the mean cutoff value of the patients and the control group was statistically significant (T = 0.135 and P value <0.05). In patient study group the ELISA test was positive in 39 of 50 (78% ) which it is highly significant when compared with noncancerous control group who were all negative 11 of 11 (100%) at p - value <0.001.Finally this study showed that (28 of 50) 56% of patients were dead because they are have invasive pulmonary aspergillosis (IPA) which is serious and potentially fatal disease that might kill the patients if any delay occurs in lab. diagnosis. So early diagnosis of invasive pulmonary aspergillosis may give higher cure rates.

دراسة التعبير الوراثي للجينات P53, KRAS, c - MYC & Her - 2/neu وانواع الرنا المايكريوية miR - 21, 34a, 92 & 98 على عينات ماخوذة من الغسول القصبي والانصباب الجنبي لمرضى مصابين بسرطان الرئة ومرضى مصابين بامراض رئوية مزمنة غير سرطانية == Expression of P53, KRAS, c - MYC, Her - 2/neu genes and microRNAs 21, 34a, 92 & 98 in cancerous and non - cancerous bronchial wash and pleural aspirate

Author name: حسين عبادي الجبوري
Supervisor name: بان عباس عبد المجيد | عدنان الجبوري
General topic: Medicine
Specific topic: Diseases
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: Background : Lung cancer is the leading cause of death from cancer in men all over the world. Most of newly diagnosed cases were in advanced stage and beyond radical treatment due to late appearance of worrying symptoms and absence of effective screening method for high risk groups. Nowadays, depending on recent advances in molecular studies researches are directed toward finding molecular markers for diagnostic, therapeutic and prognostic purposes. Aim of study : To investigate the possibility of using expression of P53, KRAS, Her - 2/neu, c - MYC and microRNAs 21, 34a, 92, and 98 as a molecular biomarkers for detection of lung cancer in samples of bronchial wash and pleural fluid. Material and Methods : A prospective case control study on a total of 120 samples, sixty bronchial washes and sixty pleural effusions. The samples were taken from patients recruited at the Thoracic Surgical Unit in the Specialized Surgery Hospital/ Medical City during the period from March 2012 to April 2014. The work was performed in the Department of pathology and forensic Medicine, Baghdad college of Medicine. The specimens were thirty bronchial wash and thirty pleural fluid samples positive for lung cancer cells by cytopathology, and similar number of negative samples. Studied genes were amplified using qRT - Realtime PCR. Housekeeping genes for normalization of mRNAs was GAPDH and RNU - 48 for microRNAs. Expression was calculated using equation; Expression = (2 - ΔΔCt). Results : Results of Ct values for each marker were obtained from Max Pro 5000 Agilent Technology PCR software and raw and standardized Ct values were analysed using SPSS - 22 software. The mean, standard deviation, t - test, ANOVA test and LSD (least significant difference) were obtained before and after normalization. A statistically significant differences in the expressions of p53, KRAS, c - MYC, Her - 2/neu and microRNAs, 21, 34a, 92, & 98 genes were found between positive and negative (control) samples with a significant p - values of <0.05. Conclusion : According to this study a conclusion could be reached; the study of expression profiles of mRNAs of P53, KRAS, c - MYC, Her - 2/neu and microRNAs 21, 34a, 92 and 98 genes can be used as a biomarker in the detection of lung cancer, differentiating subtypes, and screening of high risk groups

استخدام الصبغة المناعية p16INK4a والتهجين الموقعي وتاثيرها على فحوصات عنق الرحم الصحيحة والملتبسة == The Use of p16INK4a and In Situ Hybridization and Their Impact on the Healthy and Equivocal Pap Smears of the Cervix

Author name: ثناء جميل الخشالي
Supervisor name: ندى صالح امين | هدى مهدي الخطيب
General topic: Medicine
Degree: Doctorate
Language: English
University location: Baghdad
First pages:
Abstract: Throughout the past thirty years, the perception of cervicalcarcinoma has shifted from that of a mysteriously fatal disease, to one ofthe sexually transmitted, human papillomavirus (HPV) related infection.HPV DNA has been found in almost all cervical invasive and preinvasivecervical neoplasms.Conventional Pap smear, which was established in the early sixtiesreduced effectively the morbidity and mortality related to cervical cancer.Given the lower sensitivity of the Pap cytology test, new diagnosticparameters have been established. The histological features ofpreinvasive cervical neoplasia (CIN1, CIN2, and CIN3) are wellunderstood. However, misinterpretation of the morphological criteriacould lead to significant variability.The aim of this study is to identify women with equivocal and normalPap smear who are at risk for developing cervical cancer through the useof p16INK4a immunostaining and human papillomavirus (HPV) DNAtesting using in situ hybridization (ISH).Materials and MethodsIn order to identify human papillomavirus infection in minorcytological and histological abnormalities, biopsies collected from 60women 25 - 66 years of age with normal cervices and Pap smears (groupI), abnormal cervices and Pap smears (group II) and with cervicalcarcinoma (groupIII) referred to the Colposcopy Clinic in BaghdadTeaching Hospital - Medical City Complex, during the period from June2013 through July 2014. Cytology samples collected with ThinPrep forIVliquid base cytology (LBC), punch biopsy for histopathology formalinfixed and paraffin embedded. In situ hybridization (ISH) and p16INK4aimmunohistochemistry in addition to routine hematoxylin and eosin(H&E) stain were used to evaluate the histological specimens.ResultsThe age, age of marriage and parity of the three groups werestudied in relation to each of ISH and p16INK4a reactions. Agedistribution was highly significant among all age groups; in both ISH andp16 test results GI &GII (p=0.00), GI & GIII (p=0.00), GII &GIII(p=0.00) in both ISH and p16 test results. The age of marriage was notsignificant among the groups in both ISH and p16; GI & GII p (0.93), GI&GIII (0.12), GII &GIII (0.30). The effect of parity was insignificantamong all groups; GI & GII = (p = 0.66), GI & GIII (p = 0.82), GII &GIII (p = 0.79) in both ISH and p16 test resultsp16INK4a immunoreaction : Among group I there was a negativereaction in all the specimens collected. In specimens from group II, therewas a very mild or focal p16INK4a immunoreaction in one specimen(5%), a moderate immunoreactivity in 9 specimens (45%), and a highpositive reactivity in 10 specimens (50%) (p=0.000). Group III showedvery high immunoreaction in all the specimens collected.In situ hybridization (ISH) in group I was mild positive in 4specimens (20%) which showed diffuse signal pattern. A mild positivereaction with diffuse nuclear staining was noticed in 4 (20%) of thecervical specimens. Moderate positive reaction with diffuse staining ofthe nucleus was observed in 8 (40%) of the specimens. The remaining 8(40%) of the specimens showed both diffuse and punctate staining of theVnuclei. Among group III specimens, the nuclei in the epithelial cellsshowed both punctate and diffuse signal patterns.Chi square was done to compare results concerning ISH & variousgroups was highly significant (p= 0.00) ConclusionHPV infection is prevalent and can be missed by the conventional Pap smear. The severity of the disease was directly proportional with the age of women in this study. p16 overexpression was correlated with the positivity of ISH. This may support the use of either, or both, tests to improve the accuracy of cervical intraepithelial neoplasia (CIN) diagnosis, and help in the triage of women with equivocal lesions.

التقييم السريري ورصد قياس التاكسج خلال الليل للمرضى المعرضين لخطر توقف التنفس الانسدادي اثناء النوم == Clinical Evaluation and Overnight Oximetry Monitoring of High Risk Patients for Obstructive Sleep Apnea

Author name: محمد شاكر حسن
Supervisor name: قاسم محمد سلطان
General topic: Medicine
Specific topic: Diseases - Thoracic
Degree: Higher Diploma
Language: English
University location: Baghdad
First pages:
Abstract: Obstructive sleep apnea OSA is a condition of sleep related pharyngeal collapse, in which recurrent episodes of upper airway occlusion occur during sleep causing diminution (hypopnea) or cessation of airflow (apnea) in the pharynx provoking arousals and sleep fragmentation , resulting in daytime sleepiness. Aim of study : To evaluate patients at high risk of OSA, by clinical parameters and overnight oximetry monitoring.Patients and Method : Cross sectional study of 20 patients, 12 male and 8 female with high probability of OSA, attended to respiratory clinic in Baghdad teaching hospital suffering from excessive daytime sleepiness, they were clinically evaluated plus using overnight oximetry as an objective testing method.Results : 20 patients only complete the study, 12 male (60%), 8 female (40%), 4 patients >60 years old (20%), 9 patients 40 - 59 (45%), and 7 patients 20 - 40 (35%), smokers were 11 (55%), patients with hypertension were 8 (40%) all of them with regular anti - hypertensive drugs , 2 (10%) patients were hypothyroidism according to thyroid function test .DI show significant correlation with AHI, BMI, Baseline SPO2 and gender, while no significant correlation with age.AHI show significant correlation with baseline SPO 2 and gender, and no correlation with BMI and age.Conclusion : Desaturation index assessed by nocturnal pulse oximetry maintain its utility as a screening method in the recognition of obstructive sleep apnea in morbidly obese patients with high clinical pretest suspicion, DI > 4% when combined with appropriate clinical evaluation, could be used as an initial diagnostic test for OSA.Obesity is a major risk factor and almost all suspected patients with OSA are obese.

الاعراض السميه في الجهاز الهضمي نتيجة للعلاج الشعاعي الجذري في منطقة الحوض, الانواع, الشده والتواتر == Acute Gastrointestinal radiation toxicities in pelvic radiation therapy; types, grade and frequency

Author name: هديل ماجد علي رشيد
Supervisor name: خضير جاسم صبيح الرواق
General topic: Medicine
Specific topic: Therapeutic Radiology
Degree: Higher Diploma
Language: English
University location: Baghdad
Key words:
  • acute toxicities
  • radiation therapy
  • pelvic organ cancer.
First pages:
Abstract: نوعية الحياة للناجين من السرطان قد تتضرربصورة مباشرة بسمية الامعاء؛ نتيجة للعلاج بالاشعاع في منطقة الحوض. 12000 مريض في المملكة المتحدة يعالج سنويا بالعلاج الاشعاعي الجذري لانواع الامراض السرطانية في منطقة الحوض؛ وهذا ينطوي على مخاطر كبيرة للاثار الجانبية للانسجة المحيطة العادي. الغرض من الدراسة الهدف من هذه الدراسة هو تحديد تواتر وانواع السمية المعدية المعوية الحادة في العلاج الاشعاعي الجذري لمنطقة الحوض في بلدنا وذلك ليمكننا من اجراء مقارنة مع الغرب في هذا الصدد, بطريقة تساعدنا في تطوير الاستراتيجيات الملائمة للوقاية والعلاج. المنهجية البحث عباره عن دراسه تحليليه مستقبليه, تم اجراءها في مركز العلاج النووي والعلاج الشعاعي/ مستشفى الاورام التعليمي في مجمع مدينة الطب في بغداد, من الاول من شهر كانون الثاني ولغاية الثلاثين من شهر نيسان لسنة 2016. الدراسه شملت 53 مريضا مؤكد بالزرع النسيجي مصابين بسرطان المثانة, الرحم، وسرطان عنق الرحم، والمستقيم، وسرطان البروستاتا، يتم علاجهم بالعلاج الاشعاعي الجذرية، التحقوا جميعا بالدراسة بعد موافقة عن علم وفقا لمعايير اشتمال واستبعاد. تم تقييم المرضى للتردد، وانواع ودرجة السمية المعدية المعوية الحادة وفقا لتصنيف معايير اثار الجانبية على اساس المنظمة الاوربية للبحوث والعلاج ولجنة معايير السمية مشتركة، في بداية، خلال وفي نهاية العلاج الشعاعي. وقد تم تحليل البيانات بواسطة برنامج البرمجيات "الحزمة الاحصائية" للعلوم الاجتماعية, اصدار 20).النتيجة من اصل 53 مريضا، 60.37% (n = 32) كانت انثى و39.62% (n = 21) من الذكور. سرطان بطانة الرحم تمثل 30.18% (n = 16) من الحالات، كانت سرطانات عنق الرحم 24.52% (ن = 13)، سرطان المستقيم 11.32% (n = 6)، سرطان المثانة 24.52% (ن = 13) وسرطان البروستاتا 9.43% (ن = 5) من مجموع الحالات. الاسهال لوحظ في 27 من اصل 53 مريضا(50.9%), 15 مريض كان يعاني من الالم (28.3%) بينما الامساك والغثيان والقي مثلوا (22.6%). كان معظم السميه متمثل بالمرحله الاولى ووجد فقط مريضان بوضع المرحله الثالثه (الاسهال 4.7%). الاستنتاج تواتر وشدة السمية الحادة في الجهاز الهضمي كانت ترتبط بزيادة جرعة الاشعاع، جنبا الى جنب مع استخدام العلاج الكيميائي, والتداخل الجراحي | Background : quality of life of cancer survivors is adversely impacted by bowel toxicity; result from pelvic radiation therapy. In the UK, 12000 patients are treated with radical radiation therapy for pelvic cancer, mostly with curative intent; this carries a considerable risk for normal surrounding tissues side effects.Objective : the aim of this study was to determine the frequency and types of acute gastrointestinal toxicity in radical pelvic radiation therapy in our patients so that a comparison could be made with the West in this aspect which would help us in developing appropriate strategies for its prevention and better management. Patients and Methods : a prospective analytic study was carried out in Radiotherapy department / Oncology teaching hospital / Medical city complex, from the 2nd of January to the 30th of April 2016.A total of 53 patients with histologically confirmed uterine, cervical, rectal, urinary bladder or prostatic cancer, treated by radical radiation therapy, were enrolled in the study after informed consent according to inclusion and exclusion criteria. Patients were assessed for the frequency, types and grade of acute gastrointestinal toxicities according to grading criteria of side effect based on RTOG (Radiation Therapy Oncology Group) /EORTC (European Organization for Research and Treatment) and CTC (Common Toxicities Criteria), at the start, during and at the end of the treatment. The data was analyzed by the Statistical Package for Social Sciences (SPSS, version 20) software.Result : Diarrhea occur in 27 out of 53 patients (50.9%), 15 patients had pain (28.3%) while constipation and nausea and vomiting were 22.6% (n=12/53) each. The majority had grade 1 toxicities and only 2 patients developed grade 3 diarrhea (4.7%).Conclusion : The frequency and severity of acute gastrointestinal radiation toxicities were associated with increase dose of radiation therapy, combined with the used of chemotherapy therapy and the presence of surgery.Background : quality of life of cancer survivors is adversely impacted by bowel toxicity; result from pelvic radiation therapy. In the UK, 12000 patients are treated with radical radiation therapy for pelvic cancer, mostly with curative intent; this carries a considerable risk for normal surrounding tissues side effects.Objective : the aim of this study was to determine the frequency and types of acute gastrointestinal toxicity in radical pelvic radiation therapy in our patients so that a comparison could be made with the West in this aspect which would help us in developing appropriate strategies for its prevention and better management. Patients and Methods : a prospective analytic study was carried out in Radiotherapy department / Oncology teaching hospital / Medical city complex, from the 2nd of January to the 30th of April 2016.A total of 53 patients with histologically confirmed uterine, cervical, rectal, urinary bladder or prostatic cancer, treated by radical radiation therapy, were enrolled in the study after informed consent according to inclusion and exclusion criteria. Patients were assessed for the frequency, types and grade of acute gastrointestinal toxicities according to grading criteria of side effect based on RTOG (Radiation Therapy Oncology Group) /EORTC (European Organization for Research and Treatment) and CTC (Common Toxicities Criteria), at the start, during and at the end of the treatment. The data was analyzed by the Statistical Package for Social Sciences (SPSS, version 20) software.Result : Diarrhea occur in 27 out of 53 patients (50.9%), 15 patients had pain (28.3%) while constipation and nausea and vomiting were 22.6% (n=12/53) each. The majority had grade 1 toxicities and only 2 patients developed grade 3 diarrhea (4.7%).Conclusion : The frequency and severity of acute gastrointestinal radiation toxicities were associated with increase dose of radiation therapy, combined with the used of chemotherapy therapy and the presence of surgery.

معرفة , اتجاه وسلوك النساء الحوامل عن فقر الدم خلال الحمل في مستشفي بغداد التعليمي 2016 == Knowledge, Attitudes and Practice of Pregnant Women about Anemia during Pregnancy in Baghdad Teaching Hospital - 2016

Author name: رؤى صفاء سعيد
Supervisor name: علياء مكي حسن الصافي
General topic: Medicine
Specific topic: Family Medicine
Degree: Higher Diploma
Language: English
University location: Baghdad
First pages:
Abstract: Back ground : Anemia constitutes a public health problem worldwide, in both developed and developing countries.Aims : 1) assess the level of knowledge, attitude and practice of pregnant women about anemia 2) assess the association between knowledge of pregnant women and their socio - demographic variances 3) assess the association between the practice of pregnant women and their socio - demographic variances. Methods : The study was cross - sectional, carried out in among pregnant Baghdad Teaching Hospital, from 25th February to 28th April, 2016. A total of 300 pregnant women participated in the study. The tool of study was questionnaire. Chi - square test was used to test the statistical significance (p - value< 0.05).Results : The study revealed 63.3% of pregnant women had good knowledge, positive attitude found in 65.3% and health practice in 59.3% among pregnant women regarding anemia, the study show association between the knowledge of the pregnant woman and educational level of her and her husband, also there is association between the practice of pregnant woman and her occupation.Conclusion : A noticeable general good level of knowledge , attitude and practice among pregnant women regarding anemia during pregnancy ,level of knowledge in pregnant woman associated with the educational level of her and her husband and healthy practice increase in employed pregnant woman.Recommendations : Raise the level of knowledge and practice for prevention, learn pregnant women healthy dietary habit and encourage pregnant women to early registration in primary health care center.

تقييم مرضى توسع القصبات من الناحية السريرية والاشعاعية == Bronchiectasis Clinical and Radiological Assessment

Author name: لمى جواد كاظم
Supervisor name: مصطفى نعمة عبد علي
General topic: Medicine
Specific topic: Diseases - Thoracic
Degree: Higher Diploma
Language: English
University location: Baghdad
First pages:
Abstract: BACKGROUND : Bronchiectasis is relatively common disease in developing countries, HRCT is the method of choice for the morphologic evaluation of patients with bronchiectasis.OBJECTIVE : To assess the clinical profile of patients with bronchiectasis and evaluate the clinical relevance of high - resolution CT findings in patients with bronchiectasis by using a quantitative high - resolution CT to assess extent of bronchiectasis, severity of disease, bronchial wall thickening, and presence of smallairway abnormalities and mosaic pattern. METHODS : A cross sectional study of 50 consecutive patients with bronchiectasis in respiratory department of Baghdad teaching hospital between 1st of September 2015 and end of April 2016, clinical features of bronchiectasis and results of HRCT were assessed and correlated. RESULTS : Mean age of participants (70% males, 30% females) was 53.44 ± 9.6 years and 52% of them were lifetime non - smokers. Most common identified causes of bronchiectasis were tuberculosis (48%), pneumonia (18.4%) and cystic fibrosis (4%).The predominant symptoms were productive cough (82%), dyspnea (94%), fever (74%) and chest pain (72%). The most common findings on chest examination were crackles (86%) and wheeze (74%). Types of bronchiectasis in HRCT were cystic in 62%, varicose in 32%, tubular 6%, Involvement was multilober in 46%, diffuse in 18%and right upper lobe in 18%. Of 50 patients, 92% have bronchial wall thickening, whereas 62% show small air way abnormalities, 56%have mosaic pattern. Patients with cystic disease have significant association with productive cough with large amount of sputum, hemoptysis, Crackle and Clubbing (p < 0.05), patients with small air way abnormalities in HRCT have significant correlation with chest pain, dyspnea and amount of sputum (p < 0.05). Patient with diffuse lobe distribution on HRCT have daily significant quantities of sputum production (P < 0.05), while multilober distribution have a significant association with dyspnea and wheeze (P < 0.05).CONCLUSION : Clinical finding in patients with bronchiectasis have significant correlation with HRCT chest finding which be used for monitoring activity of disease.Key words : bronchiectasis, HRCT, amount of sputum , bronchial wall thickening, mosaic pattern. Lobes distribution

المضاعفات الرئوية بعد عمليات البطن الجراحية في الردهات الجراحية لمستشفى بغداد التعليمي == Post - abdominal surgery respiratory complications at surgical wards of Baghdad teaching hospital

Author name: رغيد حازم فاضل
Supervisor name: مصطفى نعمة عبد علي
General topic: Medicine
Specific topic: Diseases - Thoracic
Degree: Higher Diploma
Language: English
University location: Baghdad
First pages:
Abstract: Background : Postoperative pulmonary complications (PPCs) followingabdominal surgery are frequent and associated with increased morbidity andmortality, and hospital length of stay.Study objective : The aim of the study was to identify pulmonarycomplications following abdominal surgical procedures and to identifyperioperative risk factors associated with the development of thesecomplications.Patients and Methods : this is a hospitalized - based cross - sectional study. Arandomly selected sample of 52 patients who developed pulmonarysymptom(s) following abdominal surgical procedures at surgical wards ofBaghdad teaching hospital from November 2015 to June 2016. Perioperativedata were collected through interview and char review, and their associationwith the occurrence of PPCs were analyzed. Cross tabulation and Chi - squaretest were used to analyze the discrete variables and their relationship to the PPCs while one way ANOVA was used to analyze the continuous variables and their relationship to the PPCs.Results : The following PPCs were identified : 33 pneumonia, 5 acute respiratory failure, 4 basal atelectasis, 3 pleural effusion, 3 pulmonary embolism, 3 exacerbation of COPD or asthma and 1 pulmonary edema.Perioperative risk factors associated with development of PPCs were identified : current smoking history (p value = 0.042), preexisting comorbid disease (p value = 0.001), emergency surgery (p value = 0.045), upper abdominal (p value = 0.012) or both upper/lower abdominal incisions (p value = 0.026), duration of surgery ≥ 3 hours (p value = 0.049) and NG tube placement postoperatively (p value = 0.043). Conclusions : The most common PPC following abdominal surgery is pneumonia. There is no significant difference between laparoscopy and laparotomy in term of PPCs following abdominal surgery. Six perioperative risk factors associated with the occurrence of PPCs following abdominal surgery were identified which are current smoking history, preexisting comorbid diseases, emergency surgery, upper abdominal or both upper/lower abdominal incisions, duration of surgery more than or equal to three hours and NG tube placement postoperatively.

تقييم استخدام مضادات التخثر الوقائي لمنع الجلطات الدموية الوريدية في المرضى البالغين الراقدين في مستشفى بغداد التعليمي == Assessment of Prophylactic anticoagulant use for prevention of venous thromboembolism in adult inpatients at Baghdad teaching hospital

Author name: عمار محمد عبد الرضا
Supervisor name: عبد الله جنجر الفرطوسي
General topic: Medicine
Specific topic: Diseases - Thoracic
Degree: Higher Diploma
Language: English
University location: Baghdad
First pages:
Abstract: Deep venous thrombosis is one of the most problems that faces hospitalized patients and if does not treated or prevented well may lead to pulmonary embolism and it ’s complications and as a consequence increase cost effectiveness, the duration of admission and mortality.Aim of study : Evaluate the use of prophylactic anticoagulants for prevention of DVT and PE in various medical, surgical, and gynecological wards.Patients and methods : Cross sectional study of 374 patients who are indicated for VTE prophylaxis admitted to medical, surgical and gynecological wards in Baghdad teaching hospital and were assessed wither they took VTE prophylaxis or not , had any contraindications and if they developed DVT and PE during admission.Results : 374 patients involved in the study, 152 males (41%) and 222 females (59%).195 patients (52%) received VTE prophylaxis and the rest 179 patients (48%) did not received it and from the latter only 25 patients (14%) had contraindications that prevent the use of VTE prophylactic.Only 4 patients developed DVT and 1 patient developed PE in those who received VTE prophylaxis compared to 13 patients developed DVT and 7 patients developed PE in those who did not received VTE prophylaxis.There was inverse relationship between receiving VTE prophylaxis and development of DVT and PE.Conclusion : The study reveals that there was an underuse of prophylactic anticoagulants for patients who are indicated for VTE prophylaxis in medical, surgical and gynecological wards

انتشار ومتنبات الاكتئاب لدى عينة من المرضى المصابين بداء الذاب الحمامي المجموعي == Prevalence and Predictors of Depression in a Sample of patients with Systemic Lupus Erythematosus

Author name: زهراء عدنان
Supervisor name: فائق ايشو كوريال | مشتاق طالب هاشم
General topic: Medicine
Specific topic: Diseases - Joints
Degree: Higher Diploma
Language: English
University location: Baghdad
First pages:
Abstract: المرضى والطرائق : شملت الدراسة المقطعية (60) مريضا مصابا بداء الذاب الحمامي المجموعي تم تشخيصهم حسب المعاييرالمطورة التشخيصية بواسطة الكلية الامريكية لامراض الرثية.تم جمع بيانات المرضى الديموغرافية والسريرية بما في ذلك العمر والجنس ومعيار كتلة الجسم وحالة التدخين والحالة الزوجية والحالة الوضيفية واعراض سابقة لشمول الجهاز العصبي المركزي ومدة المرض وفاعلية المرض بواسطة مقياس فاعلية المرض لداء الذاب الحمامي ,الادوية المستخدمة وتحاليل الدم وشاكلة الاضداد. تم تحري جميع المرضى بواسطة المعايير التشخيصية لنوبة الاكتئاب الرئيسية د س م 5 . النتائج : نسبة انتشار الاكتئاب كانت (31.7%),نسبة الاكتاب الحاد لوحظت في (13.3%) من الحالات بينما كانت نسبة الاكتئاب المتوسط الشدة (8.3%).علاوة على ذالك الحالات الفعالة حسب مقياس فاعلية المرض لداء الذاب الحمامي12< مثلت اعلى نسب الاكتئاب(40%).مقارنتا ب(20%) لحالات المرض الخفيفة الى متوسطة الشدة.لا توجد هناك اهمية اواحصائية معتد بها للفرق في معدل فاعلية المرض لداء الذاب الحمامي بين الفئات شديدة الاكتئاب) .(p>0.05المستوى التعليمي كانت له علاقة عكسية مع الاكتئاب معتد بها احصائيا,مرضى داء الذاب الحمامي من غير تعليم رسمي كانت لهم اعلى نسب الاكتئاب (85.7%)مقارنتا لمعدل مابين (21.7%و29.4%)لمن مستوى تعليمهم اعلى.خطورة الاصابة بالاكتئاب لم تكن مختلفة في حالة وجود اوغياب اعراض تخص شمولية الجهاز العصبي المركزي بالمرض(33.3%و3.35)على التوالي.العمر والجنس والحالة الزوجية والحالة الوظيفية لايوجد لهراابط ملحوظ او معتد احصائيا مع الاكتئاب.الادوية التي سبق للمريض تعاطيها والتي تشمل اي من البريدنيزولون ,هايدروكسي كلوروكوين,سايكلوفوسفامايد ,ازاثيوبرين ,مايكوفينوليت موفتيل ,ميثوتريكسيت ,كلوروكوين ,لا توجد لها اهمية او رابط احصائي معتد مع الاكتئاب.لا توجد اهمية ملحوضة او معتدة احصائيا لتاثير وجود نتيجة ايجابية لاضداد النوى ,اضداد دي ان اي ذو الطاقين وعوز المتممة (ج3و /او ج 4)على نسبة الاصابة بالاكتاب. الاستنتاجات : نسبة الاكتئاب لدى المرضى المصابين بداء الذاب الحمامي المجموعي شائعة نسبيا.وتزداد مع زيادة فعالية المرض. المستوى التعليمي كانت له علاقة عكسية مع الاكتئاب معتد بها احصائيا. | Background : Systemic lupus erythematosus (SLE) is a multi - systemic auto immune inflammatory disease in which genetic and environmental factors implicated in its pathogenesis. Depression is a potentially life - threatening disorder that affects hundreds of millions of people all over the world. The World Health Organization has ranked depression the 4th leading cause of disability worldwide.Objectives : The aim of this study was to evaluate the prevalence and predictors of depression in a sample of Iraqi patients with SLE if present. Patients and methods : This cross - sectional study involved 60 patients with SLE diagnosed according to revised American College of Rheumatology (ACR) classification criteria. Demographics and clinical data were collected including age, sex, BMI, smoking status, marital status, unemployment, educational status, crowding index, history of CNS involvement and disease duration. Disease activity for SLE was assessed with the SLE Disease Activity Index (SLEDAI). Medications used, blood investigations and autoantibody profile were collected, all subjects were screened for depression by using the Diagnostic and statistical manual of mental disorders - 5 ( DSM5) diagnostic criteria of depression.Results : The prevalence of depression was (31.7%). A severe form of depression was observed in 13.3% of SLE cases, while a mild degree of depression was elicited in 8.3% of the cases. Furthermore, cases with a severe form of disease evaluated by SLEDAI score >12 had an obviously higher rate of depression (40%) compared to 20% among those with mild or moderate disease. There was no important or statistically significant difference in median SLEDAI score between depression severity categories (p more than 0.05). Educational level had a statistically significant negative association with depression, SLE cases with no formal education had the highest rate of depression (85.7%) compared to a rate between 21.7% and 29.4% for higher level of educational attainment. The risk of having depression was not different in the presence or absence of central nervous system (CNS) involvement (33.3% and 31.3% respectively), age, gender, marital status and employment status had no obvious or statistically significant association with depression. The history of using each of prednisolone, hydroxychloroquine, cyclophosphamide, azathioprine, mycophenylate, methotrexate and chloroquine had no important or statistically significant association with depression. Also the presence of antinuclear antibodies and anti - double stranded Deoxyribo nucleic acid (DNA) antibodies and the decrease in complement (C3 and/or C4) had no important or statistically significant effect on the presence of depression.Conclusions : The prevalence of depression in SLE patients was relatively high. SLE disease severity increase depression rate. Educational level had statistically negative association with depression
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