{"title":"Retrospective study of seven cases with acute Fatty liver of pregnancy.","authors":"Suchi Dwivedi, Ma Runmei","doi":"10.1155/2013/730569","DOIUrl":null,"url":null,"abstract":"<p><p>Objectives. Our aim is to explore the clinical outcome of patients with acute fatty liver of pregnancy (AFLP), and evaluate the effect of early diagnosis and treatment. Methods. Seven patients who were diagnosed with AFLP were retrospectively analyzed from February 2005 to January 2013. The clinical records of the patients with AFLP were reviewed for clinical features, laboratory examinations, and maternal and perinatal prognosis. Routine laboratory evaluation revealed hyperbilirubinemia, moderately elevated liver transaminase, but negative serum hepatitis virus in each patient. For additional evidence, 126 cases of AFLP were reviewed retrospectively from original articles researched in A Medline-based English and Chinese Knowledge Infrastructure between the same periods. Results. The initial symptoms of all the 7 cases with AFLP were gastrointestinal symptoms; anorexia, nausea, vomiting, and progressive jaundice. Complications revealed with renal insufficiency in all 7 patients. Hepatic failure, MODS, hypoglycemia and DIC were seen in 4 patients (57.1%). Hemorrhagic shock, ARDS, and hepatic encephalopathy were seen in 3 patients (42.8%). There was only one case of maternal death (14.2%), three cases of perinatal death (30%) and one postnatal death (10%). Conclusion. AFLP occurs in late pregnancy is a rare clinical syndrome occurs at about 36 weeks of gestation. Early diagnosis and prompt termination of pregnancy is the key of management with multidisciplinary collaboration, comprehensive treatment and effective prevention are helpful to improve prognosis of the cases with AFLP and perinatal death. </p>","PeriodicalId":73520,"journal":{"name":"ISRN obstetrics and gynecology","volume":"2013 ","pages":"730569"},"PeriodicalIF":0.0000,"publicationDate":"2013-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2013/730569","citationCount":"23","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ISRN obstetrics and gynecology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2013/730569","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2013/1/1 0:00:00","PubModel":"Print","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 23
Abstract
Objectives. Our aim is to explore the clinical outcome of patients with acute fatty liver of pregnancy (AFLP), and evaluate the effect of early diagnosis and treatment. Methods. Seven patients who were diagnosed with AFLP were retrospectively analyzed from February 2005 to January 2013. The clinical records of the patients with AFLP were reviewed for clinical features, laboratory examinations, and maternal and perinatal prognosis. Routine laboratory evaluation revealed hyperbilirubinemia, moderately elevated liver transaminase, but negative serum hepatitis virus in each patient. For additional evidence, 126 cases of AFLP were reviewed retrospectively from original articles researched in A Medline-based English and Chinese Knowledge Infrastructure between the same periods. Results. The initial symptoms of all the 7 cases with AFLP were gastrointestinal symptoms; anorexia, nausea, vomiting, and progressive jaundice. Complications revealed with renal insufficiency in all 7 patients. Hepatic failure, MODS, hypoglycemia and DIC were seen in 4 patients (57.1%). Hemorrhagic shock, ARDS, and hepatic encephalopathy were seen in 3 patients (42.8%). There was only one case of maternal death (14.2%), three cases of perinatal death (30%) and one postnatal death (10%). Conclusion. AFLP occurs in late pregnancy is a rare clinical syndrome occurs at about 36 weeks of gestation. Early diagnosis and prompt termination of pregnancy is the key of management with multidisciplinary collaboration, comprehensive treatment and effective prevention are helpful to improve prognosis of the cases with AFLP and perinatal death.
目标。我们的目的是探讨急性妊娠脂肪肝(AFLP)患者的临床预后,并评价早期诊断和治疗的效果。方法。回顾性分析2005年2月至2013年1月诊断为AFLP的7例患者。回顾了AFLP患者的临床记录,包括临床特征、实验室检查和母婴预后。实验室常规检查显示胆红素血症高,中度转氨酶升高,但血清肝炎病毒阴性。为了获得更多的证据,我们回顾性地回顾了126例AFLP病例,这些病例来自同一时期《基于medline的中英文知识基础设施》(A Medline-based English and Chinese Knowledge Infrastructure)的原始文章。结果。7例AFLP患者首发症状均为胃肠道症状;厌食,恶心,呕吐,进行性黄疸。7例患者均出现肾功能不全并发症。4例(57.1%)出现肝功能衰竭、MODS、低血糖和DIC。失血性休克、急性呼吸窘迫综合征、肝性脑病3例(42.8%)。只有1例产妇死亡(14.2%),3例围产期死亡(30%)和1例产后死亡(10%)。结论。AFLP发生在妊娠晚期,是一种罕见的临床综合征,发生在妊娠36周左右。早期诊断和及时终止妊娠是管理的关键,多学科合作,综合治疗和有效预防有助于改善AFLP患者的预后和围产期死亡。