Bahloul M, Dammak H, Khlaf-Bouaziz N, Trabelsi K, Khabir A, Ben Hamida C, Kallel H, Ksibi H, Chelly H, Chaari A, Rekik N, Bouaziz M
Service de réanimation médicale, CHU Habib-Bourguiba, route El Ain, 3029 Sfax, Tunisie.
Gynecol Obstet Fertil. 2006 Jul-Aug;34(7-8):597-606. doi: 10.1016/j.gyobfe.2006.05.013. Epub 2006 Jul 5.
To report the clinical experience, biochemical findings, complications and maternal outcome in patients with acute fatty liver of pregnancy (AFLP).
Retrospective study over a period of 11 years (1993-2003). The diagnosis of AFLP was confirmed by liver biopsy in 15 women. However, in 7 women a medical committee that took into account clinical symptoms, and laboratory findings assessed the diagnosis.
Were included in this study, 22 women with a mean age of 30+/-5.4 years. Only 22.7% of cases were primigravid. The mean gestational age was 36+/-2.76 weeks (range 31-41 weeks). The fetus was a male infant in 75% of cases. Ten women were admitted in the hospital without jaundice. However 15 women had developed an icterus since their hospital admission or during ICU stay. The mean SAPS II on the ICU admission was of 24.86+/-11.2 points. Biological disturbances observed were mainly: liver cytolysis in 91% of cases, a trend to hypoglycaemia in 86%, a hypoprotidemia in 66.7% and CIVD in 32%. During their ICU stay, 19 women (86.4%) developed one or several organ failures associated to the hepatic failure and 18 women required blood transfusion. After an average stay of 7.5 days, evolution was marked by the death of seven patients (31.8%). Factors correlated with a poor prognosis were: the delay of medical consultation, the development of jaundice, the development of encephalopathy, respiratory or a circulatory failure.
AFLP is a rare but life-threatening complication. Furthermore AFLP shares features with other more common and less perilous illnesses. An early diagnosis and appropriate therapy of this pathology should improve the poor prognosis in our country.
报告妊娠急性脂肪肝(AFLP)患者的临床经验、生化检查结果、并发症及母婴结局。
回顾性研究,为期11年(1993 - 2003年)。15名女性经肝活检确诊为AFLP。然而,7名女性由一个综合考虑临床症状和实验室检查结果的医学委员会评估诊断。
本研究纳入22名女性,平均年龄30±5.4岁。初产妇仅占22.7%。平均孕周为36±2.76周(范围31 - 41周)。75%的病例胎儿为男婴。10名女性入院时无黄疸。然而,15名女性在入院后或入住重症监护病房(ICU)期间出现黄疸。入住ICU时的平均简化急性生理学评分(SAPS II)为24.86±11.2分。观察到的生化紊乱主要有:91%的病例出现肝细胞溶解,86%有低血糖倾向,66.7%有低蛋白血症,32%有凝血因子缺乏。在ICU住院期间,19名女性(86.4%)出现与肝衰竭相关的一种或多种器官功能衰竭,18名女性需要输血。平均住院7.5天后,7名患者(31.8%)死亡。与预后不良相关的因素有:就诊延迟、黄疸出现、肝性脑病、呼吸或循环衰竭。
AFLP是一种罕见但危及生命的并发症。此外,AFLP与其他更常见、危险性较小的疾病有共同特征。对这种疾病进行早期诊断和适当治疗应能改善我国的不良预后情况。