{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,6]],"date-time":"2026-04-06T16:31:22Z","timestamp":1775493082961,"version":"3.50.1"},"reference-count":32,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2014,2,26]],"date-time":"2014-02-26T00:00:00Z","timestamp":1393372800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Obstet and Gynaecol"],"published-print":{"date-parts":[[2014,4]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Aims<\/jats:title><jats:p>Hemolysis, elevated liver enzymes and low platelet count (<jats:styled-content style=\"fixed-case\">HELLP<\/jats:styled-content>) syndrome, in its complete form, is associated with increased risk of maternal mortality and increased rate of serious obstetric complications, such as acute renal failure, hepatic failure, abruptio placentae, pulmonary edema, sepsis, hemorrhage and disseminated intravascular coagulopathy. To compare maternal and perinatal outcomes, we investigated the subsequent pregnancy outcomes and long\u2010term complications of women with partial <jats:styled-content style=\"fixed-case\">HELLP<\/jats:styled-content> (<jats:styled-content style=\"fixed-case\">pHELLP<\/jats:styled-content>) and complete <jats:styled-content style=\"fixed-case\">HELLP<\/jats:styled-content> (<jats:styled-content style=\"fixed-case\">cHELLP<\/jats:styled-content>) syndromes.<\/jats:p><\/jats:sec><jats:sec><jats:title>Material and Methods<\/jats:title><jats:p>In this retrospective study, patients complicated with <jats:styled-content style=\"fixed-case\">HELLP<\/jats:styled-content> between the years 2002 and 2007 were analyzed. <jats:styled-content style=\"fixed-case\">cHELLP<\/jats:styled-content> syndrome was defined by the presence of all of the three laboratory criteria according to the <jats:styled-content style=\"fixed-case\">T<\/jats:styled-content>ennessee <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>lassification <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>ystem. <jats:styled-content style=\"fixed-case\">pHELLP<\/jats:styled-content> syndrome was defined by the presence of one or two features of <jats:styled-content style=\"fixed-case\">HELLP<\/jats:styled-content>, but not the complete form.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Sixty\u2010four patients had <jats:styled-content style=\"fixed-case\">cHELLP<\/jats:styled-content> syndrome and 67 had <jats:styled-content style=\"fixed-case\">pHELLP<\/jats:styled-content> syndrome. Maternal complications and neonatal outcomes of the indexed pregnancies were similar. The rate of blood product transfusion was significantly higher in the <jats:styled-content style=\"fixed-case\">cHELLP<\/jats:styled-content> group (<jats:italic>P<\/jats:italic>\u2009&lt;\u20090.0001). Twenty\u2010eight patients within the <jats:styled-content style=\"fixed-case\">cHELLP<\/jats:styled-content> group and 26 within the <jats:styled-content style=\"fixed-case\">pHELLP<\/jats:styled-content> group had subsequent pregnancies with a mean interpregnancy interval of 2.9\u2009\u00b1\u20091.5 years and 2.4\u2009\u00b1\u20091.1 years, respectively. Elective termination of pregnancy (dilatation and curettage) was more frequent in the <jats:styled-content style=\"fixed-case\">cHELLP<\/jats:styled-content> group. Pre\u2010eclampsia recurrence was higher in the <jats:styled-content style=\"fixed-case\">pHELLP<\/jats:styled-content> group than in the <jats:styled-content style=\"fixed-case\">cHELLP<\/jats:styled-content> group (7.1% vs 34.6%).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Partial and complete <jats:styled-content style=\"fixed-case\">HELLP<\/jats:styled-content> syndrome are not distinct groups based on neonatal, long\u2010term and subsequent pregnancy outcomes. They probably represent a continuum in the natural evolution of the same disease.<\/jats:p><\/jats:sec>","DOI":"10.1111\/jog.12295","type":"journal-article","created":{"date-parts":[[2014,2,26]],"date-time":"2014-02-26T02:26:46Z","timestamp":1393381606000},"page":"932-940","source":"Crossref","is-referenced-by-count":26,"title":["Partial <scp>HELLP<\/scp> syndrome: Maternal, perinatal, subsequent pregnancy and long\u2010term maternal outcomes"],"prefix":"10.1111","volume":"40","author":[{"given":"Serdar","family":"Aydin","sequence":"first","affiliation":[{"name":"Obstetrics and Gynaecology Istanbul Kanuni Sultan Suleyman Research and Teaching Hospital  \u0130stanbul Turkey"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F\u0131rat","family":"Ersan","sequence":"additional","affiliation":[{"name":"Obstetrics and Gynaecology Istanbul Kanuni Sultan Suleyman Research and Teaching Hospital  \u0130stanbul 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