Comparing acute fatty liver of pregnancy from hemolysis, elevated liver enzymes, and low platelets syndrome

John J. Byrne, Angela Seasely, David B. Nelson, Donald D. Mcintire, F. Gary Cunningham

Producción científica: Articlerevisión exhaustiva

10 Citas (Scopus)

Resumen

Acute fatty liver of pregnancy (AFLP) and hemolysis, elevated liver enzymes, and low platelets (HELLP) syndrome are both associated with significant maternal and perinatal morbidity and mortality. Because of the overlap of several clinical and laboratory findings differentiation can sometimes be difficult. Both disorders have been of interest for more than 100 years, however they were not completely characterized until the early 1980s. It was not until the 1980s that AFLP and HELLP syndrome, and more specifically their clinical, laboratory, and pathologic findings, were further differentiated in the literature. More recently, the pathophysiologic mechanisms have been elucidated. In this review, we outline the similarities and differences in the clinical presentation, laboratory findings, maternal and perinatal outcomes, and clinical recovery for women diagnosed with these two syndromes. From our observations, we suggest that levels of fibrinogen, creatinine, cholesterol, and total bilirubin be used to assist with differentiating AFLP from HELLP syndrome upon admission in women presenting with either suspected disease. The rationale for identifying the specific conditions is that clinical consequences for recovery vary considerably. Specifically, AFLP is associated with significantly more hepatic and renal dysfunction as well as coagulopathy. Fortunately, both conditions can be managed with supportive measures with overall improved perinatal outcomes including morbidity and mortality.

Idioma originalEnglish (US)
Páginas (desde-hasta)1352-1362
Número de páginas11
PublicaciónJournal of Maternal-Fetal and Neonatal Medicine
Volumen35
N.º7
DOI
EstadoPublished - 2022
Publicado de forma externa

ASJC Scopus subject areas

  • Obstetrics and Gynecology
  • Pediatrics, Perinatology, and Child Health

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