2006
DOI: 10.1097/01.crd.0000174805.68081.f7
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Peripartum Cardiomyopathy

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Cited by 51 publications
(125 citation statements)
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“…Indeed, for unknown reasons, a very small percentage of patients develop dilated cardiomyopathy after pregnancy, a condition designated "peripartum cardiomyopathy." 20 Some genetically manipulated mice recapitulate this association of pregnancy and heart failure, which mechanistically has been attributed to peripartal cardiomyocyte apoptosis. 21,22 However, the cellular and molecular events that cause human peripartum cardiomyopathy remain unknown at this time.…”
Section: Fuzzy-o-logical Hypertrophy?mentioning
confidence: 99%
“…Indeed, for unknown reasons, a very small percentage of patients develop dilated cardiomyopathy after pregnancy, a condition designated "peripartum cardiomyopathy." 20 Some genetically manipulated mice recapitulate this association of pregnancy and heart failure, which mechanistically has been attributed to peripartal cardiomyocyte apoptosis. 21,22 However, the cellular and molecular events that cause human peripartum cardiomyopathy remain unknown at this time.…”
Section: Fuzzy-o-logical Hypertrophy?mentioning
confidence: 99%
“…20 The current recommendation is light exercise such as walking. 4,10 Ideal medications intrapartum include hydralazine, nitrates, digoxin, and diuretics. Angiotensinconverting enzyme inhibitors are contraindicated during pregnancy because of their teratogenicity, but these medications are the mainstay of treatment of PPCM after delivery for afterload reduction.…”
Section: Decompensated Heart Failurementioning
confidence: 99%
“…Many etiological processes have been suggested: viral myocarditis, abnormal immune response to pregnancy, maladaptive response to hemodynamic stresses of pregnancy, stress-activated cytokines, excessive prolactin excretion, and prolonged tocolysis. 4,10,17,18 Also, a familial predisposition to PPCM has been reported. [19][20][21] Although underlying genetic variants common to dilated cardiomyopathies are being proposed, 22 a genetic basis specific to PPCM has not been systematically studied.…”
mentioning
confidence: 99%
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“…Ancak ortaya göğüs ağrısı, öksürük, halsizlik, dispne, ortopne, pretibiyal ödem, el ve ayakta terleme gibi semptomlarla birlikte seyreden ve klinik bulguları konjestif kalp yetmezliği ile benzerlik gösteren ortak bir klinik tablo ortaya çıkmaktadır. 5 Olgumuzda, gebelik öncesinde ve peripartum dönemde herhangi bir kardiyak patoloji mevcut olmayıp PPCM için risk faktörü olduğu düşünülen ikiz gebelik ve HELLP sendromu ile sonuçlanan preeklampsi tablosu ve postoperatif dönemde gelişen akut kalp yetmezliği tablosu mevcuttu. Ani gelişen konjestif kalp yetmezliği klinik tablosu sonrası çekilen akciğer grafisinde akciğer ödemi tespit edilmesi, BT ile perikardiyal ve plevral efüzyon saptanması ve sonrasında uygulanan TTE sonucunda LVEF'nin <%30 olması ile hastaya PPCM tanısı konuldu.…”
Section: Olgu Sunumuunclassified