PENANGANAN TERKINI PREEKLAMSIA dr. Yusri SpOG. MKes
INTRODUCTION
EARLY ONSET PREECLAMPSIA
The Diff Differenc erences es are: Biochemical Markers Clinical Manifestation Maternal and Fetal Outcome Progn Pr ognosis osis and Com Compli plicati cation on
LATE ONSET PREECLAMPSIA
RISK FACTOR OVERLAP
EARLY-ONSET
LATE-ONSET
Fetus/ Placental Factor
Maternal Constitution
PregnancySpecific Changes
PREECLAMPSIA
De Decid cidua uall Im Immu mun n Ad Adap apta tati tion on Pr Proc oces esss
Pathophysiology In normal placental development, invasive cytotrophoblasts of fetal or origin igin invade the maternal spiral arteries, transforming them from small-caliber resistance vessels to high-caliber capacitance vessels capable of providing placental perfusion adequate to sustain the growing fetus. During the process of vascular invasion, the cytotrophoblasts differentiate from an epithelial phenotype to an endothelial phenotype, a process referred referred to as pseudovasculogenesis or vascular mimicry (top). “
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In preeclampsia, preeclampsia, cytotrophoblasts cytotrophoblasts fail to adopt an invasive endothelial phenotype. Instead, invasion of the spiral arteries is shallow, and they remain small caliber, resistance vessels (bottom).
Path Pa thop ophy hysi siol olog ogy y of L ate-Onse nset t PE Predisposed Predispo sed mater maternal nal constitution reflecting microvascu micr ovascular lar disea disease se as occurs with long-term:
Norm No rmal al pl plac acen enta ta
Angiogenesis hypertension diabetes
Endothelial Dysfunction
obesity
hyperlipidemia hyperhomosisteinemi maternal
genetic
metabolic
Preeclampsia
dysbalance
Pathophysiology of L ate-Ons nse et PE Late-onset PE is associated with the maternal pathway, but that its its association with the plac placental ental pathwa pathway y is weak or non-existent.
The two-stage theory may thus be irrelevant for the pathophysiology of late-onset late-onset PE
Pathophysiology of L ate-Onse nsett PE A weak or non-existent association between a dysfunctional/ hypoxic placenta (“the placental pathway”) and late-onset PE is supported by following findings:
Late-onset PE was not associated with small for gestational agee / IUG ag UGR R
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