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Accuracy of ultrasound in the diagnosis of lateral and posterior invasion in patients with placenta accreta spectrum disorders / Rana Ahmed Mohamed Elbarmelgy ; Supervised Abdalla Yehia Elkateb , Ahmed Mahmoud Hussein , Mohamed Faisal Ebrahim

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Rana Ahmed Mohamed Elbarmelgy , 2021Description: 91 P . : charts , facsmilies ; 25cmOther title:
  • دقة الموجات فوق الصوتية فى تشخيص اختراق المشيمة لجدارى الرحم الجانبى و الخلفى فى حالات المشيمة الملتصقة [Added title page title]
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Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Gynecology and Obstetrics Summary: Objectives: Standardized ultrasound imaging protocols have been developed for the prenatal diagnosis of placenta accreta spectrum disorders (PAS). The aim of this study was to prospectively investigate a cohort of patients at high-risk of PAS using ultrasound signs for the diagnosis of posterior and lateral accreta placentation and evaluate their effectiveness by comparing them with guided microscopic examination. Methods: A cohort of 90 consecutive patients diagnosed as PAS by prenatal ultrasound examination, who were candidates for either cesarean hysterectomy or conservative management, were investigated prospectively using the standardized description of ultrasound signs of PAS proposed by the European Working Group on abnormally invasive placenta (EW-AIP), used -when relevant-to detect posterior and lateral PAS. In all cases, the ultrasound diagnosis of posterior or lateral adhesion/invasion was compared to results of histopathological examination. Guided histologic sampling was used to target abnormally adherent/invasive areas Results: All patients had a history of 1 or more prior cesarean deliveries (CDs) and presented with a low-lying/placenta previa. The overall performance of ultrasound in the antenatal detection of lateral accreta placentation in our cohort was as follows: sensitivity, 73.58 (95% CI, 59.67 to 84.74) %; specificity, 97.30 (95% CI, 85.84 to 99.93) %; positive likelihood ratio (LR+), 27.23 (95% CI, 3.91 to 189.47); negative likelihood ratio (LR{u2013}), 0.27 (95% CI, 0.17 to 0.43) and diagnostic accuracy, 83.33% (74.00 to 90.36%)
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Item type Current library Home library Call number Copy number Status Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.15.Ph.D.2021.Ra.A (Browse shelf(Opens below)) Not for loan 01010110083679000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.15.Ph.D.2021.Ra.A (Browse shelf(Opens below)) 83679.CD Not for loan 01020110083679000

Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Gynecology and Obstetrics

Objectives: Standardized ultrasound imaging protocols have been developed for the prenatal diagnosis of placenta accreta spectrum disorders (PAS). The aim of this study was to prospectively investigate a cohort of patients at high-risk of PAS using ultrasound signs for the diagnosis of posterior and lateral accreta placentation and evaluate their effectiveness by comparing them with guided microscopic examination. Methods: A cohort of 90 consecutive patients diagnosed as PAS by prenatal ultrasound examination, who were candidates for either cesarean hysterectomy or conservative management, were investigated prospectively using the standardized description of ultrasound signs of PAS proposed by the European Working Group on abnormally invasive placenta (EW-AIP), used -when relevant-to detect posterior and lateral PAS. In all cases, the ultrasound diagnosis of posterior or lateral adhesion/invasion was compared to results of histopathological examination. Guided histologic sampling was used to target abnormally adherent/invasive areas Results: All patients had a history of 1 or more prior cesarean deliveries (CDs) and presented with a low-lying/placenta previa. The overall performance of ultrasound in the antenatal detection of lateral accreta placentation in our cohort was as follows: sensitivity, 73.58 (95% CI, 59.67 to 84.74) %; specificity, 97.30 (95% CI, 85.84 to 99.93) %; positive likelihood ratio (LR+), 27.23 (95% CI, 3.91 to 189.47); negative likelihood ratio (LR{u2013}), 0.27 (95% CI, 0.17 to 0.43) and diagnostic accuracy, 83.33% (74.00 to 90.36%)

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