INTENSIVE CARE ADMISSION IN PATIENTS WITH HELLP SYNDROME IN A TERTIARY REFERRAL HOSPITAL
نویسندگان
چکیده
منابع مشابه
Intensive care admission in patients with hellp syndrome in a tertiary referral hospital.
Results Maternal mortality rate was 14% and perinatal death occurred in 24 of 81 fetuses and newborn (30%). The most common cause of maternal complications was disseminated intravascular coagulation in 22 patients (29%), acute renal failure in 19 patients (25%), and postpartum hemorrhage in 16 patients (21%). Compared with surviving women, non-surviving women had higher mean values for internat...
متن کاملMaternal outcome in HELLP syndrome requiring intensive care management in a Turkish hospital.
CONTEXT AND OBJECTIVE Despite the development of tertiary care facilities, intensive care and advanced blood banking techniques, pregnancy-related hypertensive disorders are the main cause of maternal mortality in most countries. Our purpose was to determine maternal outcome in pregnancies complicated by HELLP syndrome (hemolysis, elevated liver enzymes and low platelet count) that required int...
متن کاملIntensive care management of the HELLP syndrome.
In 1982 Weinstein reported a syndrome in pregnancy characterized by haemolysis, elevated liver enzymes and low patelet count, the HELLP syndrome, and described it as a severe consequence of pre-eclampsia.' Patients may present with a wide variety of signs and symptoms but evidence ofpre-eclampsia may not be present.2 Multisystem failure may occur due to widespread microcirculatory dysfunction. ...
متن کاملAnalysis of Patients with Hemoptysis in a Tertiary Referral Hospital
BACKGROUND This study attempted to investigate the main causes of hemoptysis, the type of examinations used for diagnosis, the treatment modalities and outcomes. METHODS A retrospective study was conducted on the medical records of 221 patients admitted to the Chonnam National University Hospital, between January 2005 and February 2010, with hemoptysis. RESULTS Bronchiectasis (32.6%), activ...
متن کاملRobinow Syndrome: a Rare Case Report from a Tertiary Care Hospital in Eastern India
Background Robinow syndrome is a rare congenital disorder with phenotypically heterogeneous abnormalities. Two modes of inheritances are known for this syndrome namely autosomal recessive and autosomal dominant. Case Report We describe here an eighteen-month-old child who had mesomelic short stature, abnormal facial features, clinodactyly, micropenis and vertebral changes which were further sup...
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ژورنال
عنوان ژورنال: Intensive Care Medicine Experimental
سال: 2015
ISSN: 2197-425X
DOI: 10.1186/2197-425x-3-s1-a909