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![]() Vol.3, No.1, 37-38 (2011) Health doi:10.4236/health.2011.31007 Copyright © 2011 SciRes. Openly accessible at htt p://www.sci rp.org/journal / H E A LTH/ A 29-year-old pregnant woman with a history of anthracycline-induced clinical heart failure Valentina Scheggi*, Fabio Mori Department of Cardiology, Azienda Ospedaliero-Unive rsit a ria Careggi, Firenze, Italy; *Corresponding Author: v[email protected] Received 11 November 2010; revised 2 November 2010; accepted 8 November 2011 ABSTRACT The number of women with heart disease who reach childbearing age in a good functional state increases continuously as advances in diagnosis and treatment improve overall health and prognosis. The cardiologist’s role is to give the woman an estimate of both maternal and fetal risk to allow her to make an informed deci- sion about embarking on a pregnancy, and to provide appropriate antenatal care. There are only a few data about the natural history of anthracycline-induced cardiomyopathy during preg- nancy; we report our experience of a 29-year- old pregnant woman with a history of anthracycline-induced clinical heart f ai l ure. Keywords: Anthracyclines; Heart Failure; Pregnancy; Cardiomyopathy 1. INTRODUCTION Heart disease is present in 0.5-1% of all pregnancies and accounts for about 10-15% of all maternal death. Management of these patients requires teamwork of ob- stetricians, neonato logists, cardiologists, anesthetists and sometimes cardiac surgeons but there are only a few data in the literature to guide clinicians in maternal and fetal care. We report the case of a pregnant woman with anth- racycline-induced cardiomyopathy and a review of the literature. 2. METHODS We evaluated a 29-year-old woman in the 5th week of pregnancy. During childhood she had osteosarcoma treated with anthracyclines and at the age of 2 5 years she presented anthracycline-induced NYHA class IV heart failure with markedly reduced systolic left ventricular function (EF 24%) and severe mitral regurgitation. She was treated with ACE-inhibitors, beta-blockers and di- uretics with good clinical result and improving systolic left ventricular function with EF until 47% and trivial mitral regurgitation. At the time of evaluation the pulse was 83 bpm, blood pressure was 90/60 mmHg, without signs of heart failure; the electrocardiogram was normal and p-BPN was 600 pg/ml. The ACE-inhibitor was discontinued and she was treated with bisoprolol and LMWH. Her clinical conditions and left systolic ventricular function continued to be stable and she vaginally deli- vered a healthy child at 35 weeks of pregnancy. The follow up after delivery was uneventful with sta- ble EF. 3. DISCUSSION Mortality among minimally symptomatic pregnant women with cardiac disease is about 1%, as among the healthy general population. In contrast, severely symp- tomatic women have been reported to experience a mor- tality risk up to 5-15%. Just a small number of parameters allow dichotomic classification into high-risk and low -risk patients. In a prospective multicentre study enrolling 562 women, Siu et al. [1] identified poor functional NYHA class or cyanosis, left ventricular systolic dysfunction (EF < 50%), and left heart obstruction as major deter- minants for mater nal cardiac complications. Neonatal complications (20% of pregnancies) were associated with poor functional class or cyanosis, left heart obstruction, anticoagulation, smoking, and multiple gestations. Vere na Stangl et al. [2] found that women at high-risk (as defined above) had a 6.1-fold higher maternal com- plication rate and a 6.1 times higher fetal/neonatal event rate; 64.7% of the high-risk women delivered prema- turely, compared to 16.4% in the low-ris k group. ![]() V. Scheggi et al. / Ntural Science 3 (2011) 37-38 Copyright © 2011 SciRes. Openly accessible at http:/ /www.scir p.org/journal/HEA LTH/ 38 In low-risk women, fetal complications were compa- rable to those reported for the general population but preterm birth rate was slightly higher. Thorne et al. [3] showed that the risk of maternal death is approximately 7% if the patient is in New York Heart Association (NYHA) functional class III or IV. Other adverse risk factors include ejection fraction < 20%, mitral regurgitation, right ventricular failure, atrial fibrillation, and systemic hypotension. The natural history of specific types of cardiomyopa- thy during pregnancy is unknown and there are only a few data about pregnant women with anthracycline-in- duced cardiomyopathy. Anthracycline-cardiotoxicity can become manifest as either clinical heart failure or asymptomatic cardiac dysfunction. Both can develop also years after the cessa- tion of treatment, as happened in our patient. Elvira C. van Dalen [4] evaluated the incidence of pe- ripartum anthracycline-induced clinical heart failure in a cohort of 53 women. This study demonstrates a low risk in childhood cancer survivors. It is worth noticing that 2 of the 53 women included in this study developed heart failure shortly after the end of anthracycline therapy and that neither of them developed any peripartum cardiac problems. About therapy, sodium and physical activity restric- tions, in association with drugs like digoxin and furose- mide, help control heart failure during pregnancy. Hydralazine, with or w ithout nitrates, is an alternative to angiotensin-converting enzyme inhibitors, that are associated with side effects. As anti-arrhythmics, amiodarone may be toxic but beta-blockers c a n be us ed safel y. Finally, patients with ventricular dysfunction must be anticoagulated with heparin at prophylactic doses to prevent thromboembolism. 4. CONCLUSION In summary, pregnancy outcome in women who re- ceived anthracyclines for malignancy in childhood is generally favorable. Th ose with left ventricular dysfunc- tion, as our patient, should be considered at increased risk but probably the most important prognostic f actor is the NYHA class. REFERENCES [1] Siu, S.C., Sermer, M., Colman, J.M., Alvarez, A.N., Mercier, L.-A., Morton, B.C., Kells, C.M., Bergin, M.L., Kiess, M.C., Marcotte, F., Taylor, D.A., Gordon, E.P., Spears, J.C., Tam, J.W., Amankwah, K.S., Smallhorn, J.F., Farine, D. and Sorensen, S. (2001) Prospective multicenter study of pregnancy outcomes in women with heart disease. Circulation, 104, 515-521. doi:10.1161/hc3001.093437 [2] Stangl, V., Schad, J., Gossing, G., Borge s, A., Baumann, G., Stangl, K. (2008) Maternal heart disease and preg- nancy outcome: A single-centre experience. European Journal of Heart Failure, 10, 855-860. doi:10.1016/j.ejheart.2008.07.017 [3] Thorne, S.A. (2004) Pregnancy in heart disease. Heart, 90, 450-456. doi:10.1136/hrt.2003.027888 [4] Dalen, E.C.V, Pal, H.J.H.V.D. , Bos, C.V. D. , Kok, W.E.M., Caron, H.N. and Kremer, L.C.M.. Clinical heart failure during pregnancy and delivery in a cohort of female childhood cancer survivors treated with anthra- cyclines (2006) European Journal of Cancer, 42, 2549- 2553. doi:10.1016/j.ejca.2006.04.014 |



