Peripartum Kardiyomiyopatide Klinik Karar Süreci: Olgu Temelli Yaklaşım

Yazarlar

Selda Murat

Özet

Peripartum kardiyomiyopati, gebeliğin son döneminde veya doğum sonrası aylarda ortaya çıkan, etiyolojisi açıklanamayan sol ventrikül sistolik disfonksiyonu ile karakterize, nadir ancak potansiyel olarak yaşamı tehdit eden bir kardiyomiyopatidir ve fizyolojik postpartum semptomlarla örtüşmesi nedeniyle tanı sıklıkla gecikmektedir. Bu olgu sunumunda, doğumdan üç ay sonra dispne, ortopne ve periferik ödem yakınmaları ile başvuran 22 yaşındaki bir kadın hastada peripartum kardiyomiyopati tanı ve yönetimi sunulmaktadır. Transtorasik ekokardiyografide ileri derecede sol ventrikül sistolik disfonksiyonu ve apikal intrakaviter trombüs saptanmış, klinik ve diğer tanısal değerlendirmelerle sekonder nedenler dışlanmıştır. Hastaya intravenöz diüretik tedavi ile birlikte kılavuz temelli kalp yetersizliği tedavisi başlanmış ve trombüs varlığı nedeniyle antikoagülan tedavi uygulanmıştır. Tedavi sürecinde semptomlarda belirgin gerileme sağlanarak hasta klinik olarak stabil durumda taburcu edilmiştir. Bu olgu, postpartum dönemde gelişen kalp yetersizliği semptomlarının dikkatle değerlendirilmesi ve erken kardiyak görüntülemenin tanı ve tedavi açısından kritik önemini vurgulamaktadır.

Peripartum cardiomyopathy is a rare but potentially life-threatening cardiomyopathy characterized by unexplained left ventricular systolic dysfunction occurring in the last months of pregnancy or during the postpartum period. Because its clinical manifestations may overlap with physiological postpartum symptoms, diagnosis is frequently delayed. In this case report, we present the diagnostic and therapeutic management of a 22-year-old woman admitted with dyspnea, orthopnea, and peripheral edema three months after delivery. Transthoracic echocardiography demonstrated severe left ventricular systolic dysfunction accompanied by an apical intracavitary thrombus, while secondary causes of cardiomyopathy were excluded through clinical and diagnostic evaluation. The patient was treated with intravenous diuretic therapy and guideline-directed heart failure treatment, and anticoagulant therapy was initiated because of the presence of left ventricular thrombus. Significant symptomatic improvement was achieved during hospitalization, and the patient was discharged in clinically stable condition. This case highlights the importance of careful evaluation of postpartum heart failure symptoms and emphasizes the critical role of early cardiac imaging in the diagnosis and management of peripartum cardiomyopathy.

Referanslar

De Backer J, Haugaa KH, Hasselberg NE, de Hosson M, Brida M, Castelletti S, et al; ESC Scientific Document Group. 2025 ESC Guidelines for the management of cardiovascular disease and pregnancy. Eur Heart J. 2025 Nov 14;46(43):4462-4568. doi: 10.1093/eurheartj/ehaf193. Erratum in: Eur Heart J. 2026 Feb 18;47(7):812.

Bauersachs J, König T, van der Meer P, Petrie MC, Hilfiker-Kleiner D, Mbakwem A, et al. Pathophysiology, diagnosis and management of peripartum cardiomyopathy: a position statement from the Heart Failure Association of the European Society of Cardiology study group on peripartum cardiomyopathy. Eur J Heart Fail 2019;21: 827–43.

Arany Z. Peripartum cardiomyopathy. N Engl J Med 2024;390:154–64.

Ware JS, Li J, Mazaika E, Yasso CM, DeSouza T, Cappola TP, et al. Shared genetic predisposition in peripartum and dilated cardiomyopathies. N Engl J Med 2016;374: 233–41.

Goli R, Li J, Brandimarto J, Levine LD, Riis V, McAfee Q, et al. Genetic and phenotypic landscape of peripartum cardiomyopathy. Circulation 2021;143:1852–62.

Mielniczuk LM, Williams K, Davis DR, Tang AS, Lemery R, Green MS, et al. Frequency of peripartum cardiomyopathy. Am J Cardiol 2006;97(12):1765–8.

Brar SS, Khan SS, Sandhu GK, Jorgensen MB, Parikh N, Hsu JW, et al. Incidence, mortality, and racial differences in peripartum cardiomyopathy. Am J Cardiol 2007;100(2): 302–4.

Karaye KM, Ishaq NA, Sa’idu H, Balarabe SA, Talle MA, Isa MS, et al. Incidence, clinical characteristics, and risk factors of peripartum cardiomyopathy in Nigeria: results from the PEACE registry. ESC Heart Fail 2020;7(1):235–43.

Patten IS, Rana S, Shahul S, Rowe GC, Jang C, Liu L, et al. Cardiac angiogenic imbalance leads to peripartum cardiomyopathy. Nature 2012;485:333–8.

Ricke-Hoch M, Pfeffer TJ, Hilfiker-Kleiner D. Peripartum cardiomyopathy: basic mechanisms and hope for new therapies. Cardiovasc Res 2020;116:520–31.

Sliwa K, Hilfiker-Kleiner D, Damasceno A, Al Farhan H, Goland S, Johnson MR, et al. Peripartum cardiomyopathy. Lancet. 2025 Nov 22;406(10518):2483-2493.

Sigauke FR, Ntsinjana H, Tsabedze N. Peripartum cardiomyopathy: a comprehensive and contemporary review. Heart Fail Rev. 2024 Nov;29(6):1261-1278.

Sliwa K, Bauersachs J, Arany Z, Spracklen TF, Hilfiker-Kleiner D. Peripartum cardiomyopathy: from genetics to management. Eur Heart J 2021;42:3094–102.

Xu H, Zhao L, Fu H, Xu R, Xie L, Zhang K, et al. Prognostic Value of Cardiac MRI Late Gadolinium Enhancement in Patients with Peripartum Cardiomyopathy: A Retrospective Study. Curr Probl Cardiol. 2023;48(4):101587.

Schelbert EB, Elkayam U, Cooper LT, Givertz MM, Alexis JD, Briller J, et al. Myocardial damage detected by late gadolinium enhancement cardiac magnetic resonance is uncommon in peripartum cardiomyopathy. J Am Heart Assoc 2017;6:e005472.

Heidenreich PA, Bozkurt B, Aguilar D, Allen LA, Byun JJ, Colvin MM, et al. 2022 AHA/ACC/HFSA Guideline for the Management of Heart Failure: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. J Am Coll Cardiol. 2022;79(17):e263-e421. doi: 10.1016/j.jacc.2021.12.012. Epub 2022 Apr 1. Erratum in: J Am Coll Cardiol. 2023;81(15):1551.

Davis MB, Arany Z, McNamara DM, et al. Peripartum cardiomyopathy: JACC state-of-the-art review. J Am Coll Cardiol. 2020;75:207–221.

McDonagh TA, Metra M, Adamo M, Gardner RS, Baumbach A, Böhm M, et al. ESC Scientific Document Group. 2023 Focused Update of the 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure. Eur Heart J. 2023;44(37):3627-3639. doi: 10.1093/eurheartj/ehad195. Erratum in: Eur Heart J. 2024;45(1):53.

Lin Y, Zhang H, Zhao S, Chen L, Li J, Wang X, et al. The efficacy and safety of the combined therapy of sodium-glucose co-transporter-2 inhibitors and angiotensin receptorneprilysin inhibitor in patients with heart failure with reduced ejection fraction: a meta-analysis of the EMPEROR-reduced and DAPA-HF sub-analysis. Front Cardiovasc Med 2022;9:882089.

Piotrkowicz E, Skrzypczyk P, Prejbisz A, Dobrowolski P, Gawlak M, Kosiński P. Safety and Risks of Antihypertensive Medications During Breastfeeding: A Review of Current Guidelines. J Clin Med. 2025 May 26;14(11):3722.

Hilfiker-Kleiner D, Haghikia A, Berliner D, Vogel-Claussen J, Schwab J, Franke A, et al. Bromocriptine for the treatment of peripartum cardiomyopathy: a multicentre randomized study. Eur Heart J 2017;38:2671–2679.

Jha N, Jha AK. Peripartum cardiomyopathy. Heart Fail Rev. 2021;26(4):781-797.

Chaudhari K, Choudhary M, Chaudhari K, Verma N, Kumar S, Madaan S, et al. Advancement in Current Therapeutic Modalities in Postpartum Cardiomyopathy. Cureus. 2022;14(3):e22813.

Sliwa K, Petrie MC, van der Meer P, Mebazaa A, Hilfiker-Kleiner D, Jackson AM, et al. Clinical presentation, management, and 6-month outcomes in women with peripartum cardiomyopathy: an ESC EORP registry. Eur Heart J 2020;41:3787–97.

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5 Ağustos 2026

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