Abstract
Background:
Peripartum cardiomyopathy is an idiopathic disorder defined by the occurrence of acute heart failure during late pregnancy or post-partum period in the absence of any other definable cause. Its clinical course is variable and severe cases might require heart transplantation.
Objective:
To investigate long-term outcomes after heart transplantation (HT) for peripartum cardiomyopathy (PPCM).
Methods:
Out of a single-center series of 1938 HT, 14 HT were performed for PPCM. We evaluated clinical characteristics, transplant-related complications, and long-term outcomes, in comparison with 28 sex-matched controls. Primary endpoint was death from any cause; secondary endpoints were transplant-related complications (rejection, infection, cardiac allograft vasculopathy). A value of p < 0.05 was considered of statistical significance.
Results:
PPCM patients and matched controls were comparable for most variables (all p values > 0.05), except for a higher use of inotropes at the time of HT in PPCM group (p = 0.03). During a median follow-up of 7.7 years, 16 patients died, 3 (21.5%) in PPCM group and 13 (46.5%) in control group. Mortality was significantly lower in PPCM group (p = 0.03). No significant difference was found in terms of transplant-related complications (p > 0.05).
Conclusions:
Long-term outcomes following HT for PPCM are favorable. Heart transplantation is a valuable option for PPCM patients who did not recover significantly under medical treatment.
Keywords:
Heart Failure; Cardiomyopathies / mortality; Peripartum Period; Heart Transplantation; Graft Rejection. / mortality
Resumo
Fundamento:
A cardiomiopatia periparto é uma doença idiopática definida pela ocorrência de insuficiência cardíaca aguda durante a gravidez tardia ou pós-parto na ausência de qualquer outra causa definível. Seu curso clínico é variável e casos graves podem exigir transplante. cardíaco.
Objetivo:
Pesquisar os resultados a longo prazo após transplante cardíaco (TC) por cardiomiopatia periparto (CMPP).
Métodos:
De uma única série central de 1938 TC, 14 TC foram realizados por CMPP. Foram avaliadas características clínicas, complicações relacionadas ao transplante e resultados a longo prazo, em comparação com 28 controles pareados por gênero. O principal critério de avaliação foi a morte por qualquer causa; os critérios secundários foram complicações relacionadas ao transplante (rejeição, infecção, vasculopatia do aloenxerto cardíaco). Um valor de p < 0,05 foi considerado estatisticamente significante.
Resultados:
As pacientes com CMPP e controles pareados foram comparáveis para a maioria das variáveis (todos os valores de p > 0,05), exceto para um maior uso de inotrópicos no momento do TC no grupo CMPP (p = 0,03). Durante um seguimento médio de 7,7 anos, 16 pacientes morreram, 3 (21,5%) no grupo CMPP e 13 (46,5%) no grupo controle. A mortalidade foi significativamente menor no grupo CMPP (p = 0,03). Não foram encontradas diferenças significativas em termos de complicações relacionadas ao transplante (p> 0,05).
Conclusões:
Os resultados a longo prazo após TC para CMPP são favoráveis. O transplante cardíaco é uma opção valiosa para pacientes com CMPP que não se recuperaram significativamente sob tratamento médico.
Palavras-chave:
Insuficiência Cardíaca; Cardiomiopatias / mortalidade; Período Periparto; Transplante de Coração; Rejeição de Enxerto / mortalidade
Introduction
Peripartum cardiomyopathy (PPCM) is defined by the occurrence of acute heart failure (HF) during late pregnancy or post-partum period in the absence of any other definable cause or prior heart disease. Diagnostic criteria have recently been revised by the ESC Working Group on PPCM.11 Sliwa K, Hilfiker-Kleiner D, Petrie MC, Mebazaa A, Pieske B, Buchmann E, et al. Heart Failure Association of the European Society of Cardiology Working Group on Peripartum Cardiomyopathy. Current state of knowledge on aetiology, diagnosis, management, and therapy of peripartum cardiomyopathy: a position statement from the Heart Failure Association of the European Society of Cardiology Working Group on peripartum cardiomyopathy. Eur J Heart Fail. 2010;12(8):767-78. doi: 10.1093/eurjhf/hfq120.
https://doi.org/10.1093/eurjhf/hfq120...
Disease incidence shows ethnic variations, with a greater prevalence among African women.22 Fett JD, Christie LG, Carraway RD, Murphy JG. Five-year prospective study of the incidence and prognosis of peripartum cardiomyopathy at a single institution. Mayo Clin Proc. 2005;80(12):1602-6. doi: 10.4065/80.12.1602.
https://doi.org/10.4065/80.12.1602...
A deleterious combination of “anti angiogenic signaling excess” and “oxidative stress-prolactin axis” toward the end of pregnancy is suggested as key element in the pathophysiology of the disease.33 Hilfiker-Kleiner D, Sliwa K. Pathophysiology and epidemiology of peripartum cardiomyopathy. Nat Rev Cardiol. 2014;11(6):364-70. doi: 10.1038/nrcardio.2014.37.
https://doi.org/10.1038/nrcardio.2014.37...
Beside conventional treatment of HF,44 Ponikowski P, Voors AA, Anker SD, Bueno H, Cleland JG, Coats AJ, et al; Authors/Task Force Members. 2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: The Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC). Developed with the special contribution of the Heart Failure Association (HFA) of the ESC. Eur J Heart Fail. 2016;18(8):891-975. doi: 10.1002/ejhf.592.
https://doi.org/10.1002/ejhf.592...
targeted therapies including pharmacological prolactin blockade are being investigated.55 Sliwa K, Blauwet L, Tibazarwa K, Libhaber E, Smedema JP, Becker A, et al. Evaluation of bromocriptine in the treatment of acute severe peripartum cardiomyopathy: a proof-of-concept pilot study. Circulation. 2010;121(13):1465-73. doi: 10.1161/CIRCULATIONAHA.109.901496.
https://doi.org/10.1161/CIRCULATIONAHA.1...
Although half of patients will fully recover left ventricular systolic function, the clinical course of PPCM is highly variable.66 McNamara DM, Elkayam U, Alharethi R, Damp J, Hsich E, Ewald G, et al; IPAC Investigators. Clinical outcomes for peripartum cardiomyopathy in North America: results of the IPAC Study (Investigations of Pregnancy-Associated Cardiomyopathy). J Am Coll Cardiol. 2015;66(8):905-14. doi: 10.1016/j.jacc.2015.06.1309.
https://doi.org/10.1016/j.jacc.2015.06.1...
,77 Goland S, Bitar F, Modi K, Safirstein J, Ro A, Mirocha J, et al. Evaluation of the clinical relevance of baseline left ventricular ejection fraction as a predictor of recovery or persistence of severe dysfunction in women in the United States with peripartum cardiomyopathy. J Card Fail. 2011;17(5):426-30. doi: 10.1016/j.cardfail.2011.01.007.
https://doi.org/10.1016/j.cardfail.2011....
Data from the Investigations of Pregnancy-Associated Cardiomyopathy (IPAC) recently assessed a 6% rate of death, heart transplantation, and left ventricular assist device (LVAD) implantation at 1 year in PPCM patients and more than 20% rate of persistent left ventricular (LV) dysfunction.66 McNamara DM, Elkayam U, Alharethi R, Damp J, Hsich E, Ewald G, et al; IPAC Investigators. Clinical outcomes for peripartum cardiomyopathy in North America: results of the IPAC Study (Investigations of Pregnancy-Associated Cardiomyopathy). J Am Coll Cardiol. 2015;66(8):905-14. doi: 10.1016/j.jacc.2015.06.1309.
https://doi.org/10.1016/j.jacc.2015.06.1...
Baseline LVEF < 30%, baseline LV end-diastolic diameter (LVEDD) > 60mm, black ethnicity and post-partum diagnosis were correlated with poor prognosis.66 McNamara DM, Elkayam U, Alharethi R, Damp J, Hsich E, Ewald G, et al; IPAC Investigators. Clinical outcomes for peripartum cardiomyopathy in North America: results of the IPAC Study (Investigations of Pregnancy-Associated Cardiomyopathy). J Am Coll Cardiol. 2015;66(8):905-14. doi: 10.1016/j.jacc.2015.06.1309.
https://doi.org/10.1016/j.jacc.2015.06.1...
Up to 10% of PPCM patients will require heart transplantation according to literature data.66 McNamara DM, Elkayam U, Alharethi R, Damp J, Hsich E, Ewald G, et al; IPAC Investigators. Clinical outcomes for peripartum cardiomyopathy in North America: results of the IPAC Study (Investigations of Pregnancy-Associated Cardiomyopathy). J Am Coll Cardiol. 2015;66(8):905-14. doi: 10.1016/j.jacc.2015.06.1309.
https://doi.org/10.1016/j.jacc.2015.06.1...
,88 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. doi: 10.1016/j.amjcard.2006.01.039.
https://doi.org/10.1016/j.amjcard.2006.0...
9 Duran N, Günes H, Duran I, Biteker M, Ozkan M. Predictors of prognosis in patients with peripartum cardiomyopathy. Int J Gynaecol Obstet. 2008;101(2):137-40. doi: 10.1016/j.ijgo.2007.11.007.
https://doi.org/10.1016/j.ijgo.2007.11.0...
-1010 Amos AM, Jaber WA, Russell SD. Improved outcomes in peripartum cardiomyopathy with contemporary. Am Heart J. 2006;152(3):509-13. doi: 10.1016/j.ahj.2006.02.008.
https://doi.org/10.1016/j.ahj.2006.02.00...
Post-transplant prognosis for PPCM patients is at present still contradictory.1111 Rickenbacher PR, Rizeq MN, Hunt SA, Billingham ME, Fowler MB. Long-term outcome after heart transplantation for peripartum cardiomyopathy. Am Heart J. 1994;127(5):1318-23. PMID: 8172060.
12 Keogh A, Macdonald P, Spratt P, Marshman D, Larbalestier R, Kaan A. Outcome in peripartum cardiomyopathy after heart transplantation. J Heart Lung Transplant. 1994;13(2):202-7. PMID: 8031800.
13 Rasmusson K, Brunisholz K, Budge D, Horne BD, Alharethi R, Folsom J, et al. Peripartum cardiomyopathy: post-transplant outcomes from the United Network for Organ Sharing Database. J Heart Lung Transplant. 2012;31(2):180-6. doi: 10.1016/j.healun.2011.11.018.
https://doi.org/10.1016/j.healun.2011.11...
-1414 Rasmusson KD, Stehlik J, Brown RN, Renlund DG, Wagoner LE, Torre-Amione G, et al; Cardiac Transplant Research Database Group. Long-term outcomes of cardiac transplantation for peri-partum cardiomyopathy: a multiinstitutional analysis. J Heart Lung Transplant. 2007;26(11):1097-104. doi: 10.1016/j.healun.2007.08.002.
https://doi.org/10.1016/j.healun.2007.08...
A higher incidence of rejection has been reported, particularly during the first year following transplantation, along with a lower graft survival.1313 Rasmusson K, Brunisholz K, Budge D, Horne BD, Alharethi R, Folsom J, et al. Peripartum cardiomyopathy: post-transplant outcomes from the United Network for Organ Sharing Database. J Heart Lung Transplant. 2012;31(2):180-6. doi: 10.1016/j.healun.2011.11.018.
https://doi.org/10.1016/j.healun.2011.11...
,1414 Rasmusson KD, Stehlik J, Brown RN, Renlund DG, Wagoner LE, Torre-Amione G, et al; Cardiac Transplant Research Database Group. Long-term outcomes of cardiac transplantation for peri-partum cardiomyopathy: a multiinstitutional analysis. J Heart Lung Transplant. 2007;26(11):1097-104. doi: 10.1016/j.healun.2007.08.002.
https://doi.org/10.1016/j.healun.2007.08...
Heart transplantation (HT) is however considered as a valuable option for PPCM patients presenting with HF unresponsive to maximal conventional treatment. The aim of this study is to compare all-cause mortality and transplant-related complications after HT for PPCM.
Methods
This is a retrospective single-center non-interventional study. Primary endpoint was all-cause mortality following heart transplantation (HT). Secondary endpoint was outcomes after HT including transplant-related complications (rejection, infection, cardiac allograft vasculopathy). All patients had single-center management with a consistent approach at both surgical and medical levels.
Patient population
A total of 1938 patients from whom 368 females were transplanted for severe HF in our institution. Fourteen patients met diagnosis criteria of PPCM. All our PPCM cases were ascertained with the most recent definition of the disease.11 Sliwa K, Hilfiker-Kleiner D, Petrie MC, Mebazaa A, Pieske B, Buchmann E, et al. Heart Failure Association of the European Society of Cardiology Working Group on Peripartum Cardiomyopathy. Current state of knowledge on aetiology, diagnosis, management, and therapy of peripartum cardiomyopathy: a position statement from the Heart Failure Association of the European Society of Cardiology Working Group on peripartum cardiomyopathy. Eur J Heart Fail. 2010;12(8):767-78. doi: 10.1093/eurjhf/hfq120.
https://doi.org/10.1093/eurjhf/hfq120...
An extensive work-up was performed retrospectively for each patient to exclude other causes of HF. Twenty-eight age-matched female patients who underwent HT during the same period for other causes served as controls. Each PPCM patient was matched to two female control patients depending on their age at the time of transplantation (± 5 years) and on the era of transplantation (± 6 months). Survival was assessed until last follow-up. Demographics, pre- and post-transplant data were retrospectively collected from our institution’s computerized medical charts. Information on follow-up was obtained retrospectively by direct patient interview for those who were still alive at the time of data collection. As this was an observational study, our institutional ethics board was not involved.
Post-transplant course
All patients had a similar post-transplant follow-up protocol. Endomyocardial biopsies were routinely performed during the first two years following HT, then, less frequently (every 6 months for years 2 to 5, then every year beyond 5th year), unless clinical indication. Coronary angiography was first performed at one-year post transplant then every two years if normal. We considered arbitrarily graft rejection as present or non-present, regardless of its type (antibody-mediated or cell-mediated rejection) and severity. The diagnosis of cell mediated rejection was based on Stanford grading system until 1990,1515 Billingham ME. Dilemma of variety of histopathologic grading systems for acute cardiac allograft rejection by endomyocardial biopsy. J Heart Transplant. 1990;9(3 Pt 2):272-6. PMID: 2355282. then, on the International Society for Heart and Lung Transplantation nomenclature (ISHLT;1616 Stewart S, Winters GL, Fishbein MC, Tazelaar HD, Kobashigawa J, Abrams J, et al. Revision of the 1990 working formulation for the standardization of nomenclature in the diagnosis of heart rejection. J Heart Lung Transplant. 2005;24(11):1710- 20. doi: 10.1016/j.healun.2005.03.019.
https://doi.org/10.1016/j.healun.2005.03...
). The ISHLT Guidelines on Antibodies-mediated rejection (AMR) were used for the definition of AMR rejections.1717 Kobashigawa J, Crespo-Leiro MG, Ensminger SM, Reichenspurner H, Angelini A, Berry G, et al; Consensus Conference Participants. Consensus Conference Participants. Report from a consensus conference on antibody-mediated rejection in heart transplantation. J Heart Lung Transplant. 2011;30(3):252-69. doi: 10.1016/j.healun.2010.11.003.
https://doi.org/10.1016/j.healun.2010.11...
,1818 Berry GJ, Burke MM, Andersen C, Bruneval P, Fedrigo M, Fishbein MC, et al. The 2013 International Society for Heart and Lung Transplantation Working Formulation for the standardization of nomenclature in the pathologic diagnosis of antibody-mediated rejection in heart transplantation. J Heart Lung Transplant. 2013;32(12):1147-62. doi: 10.1016/j.healun.2013.08.011.
https://doi.org/10.1016/j.healun.2013.08...
We considered rejection as “characterized” in the following situations: All cell-mediated rejections of grade > or = to 1A/1R; All proven antibodies mediated rejection regardless of grade; All symptomatic rejections i.e. with hemodynamic compromise or LV dysfunction.1919 Stobierska-Dzierzek B, Awad H, Michler RE. The evolving management of acute right-sided heart failure in cardiac transplant recipients. J Am Coll Cardiol. 2001;38(4):923-31. PMID: 11583860. All characterized rejections triggered therapeutic interventions.
Cardiac Allograft Vasculopathy (CAV) was considered in the setting of any angiographic evidence of coronary artery stenosis regardless of the need of specific treatment.2020 Mehra MR, Crespo-Leiro MG, Dipchand A, Ensminger SM, Hiemann NE, Kobashigawa JA, et al. International Society for Heart and Lung Transplantation working formulation of a standardized nomenclature for cardiac allograft vasculopathy-2010. J Heart Lung Transplant. 2010;29(7):717-27. doi: 10.1016/j.healun.2010.05.017. Erratum in: J Heart Lung Transplant. 2011;30(3):360.
https://doi.org/10.1016/j.healun.2010.05...
Infections were defined as any episode requiring hospitalization or intravenous treatment, including cytomegalovirus (CMV) infections.
Immunosuppressive therapy and rejection treatments varied over time. Induction therapy involved intravenous methylprednisolone, and rabbit anti-thymocyte globulin from 1986 to 2000; and antithymocyte globulin or Basiliximab since 2000. Long-term prophylactic immunosuppressive therapy was based on calcineurin inhibitors (mostly cyclosporine), azathioprine and long-term oral corticosteroids from 1986 to 2000; and calcineurin inhibitors (cyclosporine or tacrolimus), mycophenolate mofetil and oral corticosteroids since 2000. Everolimus was not routinely used upon the study population. Of note, none of the patients in PPCM group received Bromocriptine.
Statistical considerations and analysis
Data are presented as the mean ± standard deviation, unless otherwise specified. Comparisons between groups for continuous variables were performed using the Student t-test or the Mann Whitney U test as appropriate. The chi-square or the Fisher exact tests were used for categorical variables as appropriate. The duration of follow up was computed using reverse the Kaplan Meier method. Survival was defined as being alive at the cut-off date for our study without the need of a retransplantation. Kaplan-Meier survival curves were constructed for the two groups and compared using the log rank test. A value of p < 0.05 was considered of statistical significance. All analyses were conducted with the use of SPSS 18.0 software (Chicago, Illinois).
Results
Pre-transplant characteristics
Pre-transplant characteristics are summarized in Tables 1 and 2. Patients in control group were transplanted for: idiopathic dilated (n = 10, 36%), ischemic (n = 8, 28.5%), congenital (n = 1, 3.5%), restrictive (n = 2, 7.1%), valvular (n = 2, 7.1%), and anthracyclines-induced (n = 3, 10.7%) cardiomyopathies or myocarditis (n = 2, 7.1%). There were significantly more patients requiring inotropes in PPCM group (n= 9, 64% in PPCM patients vs. n = 8, 28% in controls, p = 0.03). Patients requiring hemodynamic support were indiscriminately those recently diagnosed with PPCM and readily presenting with cardiogenic shock (n = 4/9), but also those with long time known PPCM and gradually progressing to end-stage heart failure (n = 5/9). Conversely, in control group, patients requiring inotropic support were more often those who were recently (< 1year) diagnosed with HF.
We found no significant difference considering African descent; the time spent on the transplant waiting list; right ventricular dysfunction; and HF severity at the time of diagnosis. No significant difference in HF treatment was noticed particularly in terms of ACE inhibitors or beta-blockers administration, and cardiac resynchronization therapy (CRT) / internal cardioverter defibrillator (ICD) implantation rates.
Regarding mechanical circulatory support (MCS) indication, no significant difference was observed. In PPCM group, one patient underwent intra-aortic balloon counterpulsation (IABP), two peripheral Extra-Corporeal Membrane Oxygenation (ECMO), one long-term Ventricular Assist Devices, and one CardioWest Total Artificial Heart implantation. In control group, two patients underwent IABP, seven peripheral or central ECMO, and two long term VADs.
Graft Characteristics and Immunosuppressive treatments
Graft characteristics were similar in the two groups. Mean ischemic time duration was 159 ± 12 minutes in PPCM group vs. 178 ± 13 minutes in control group. Mean age donor was 45 years for PPCM recipients and 46 years for controls. We observed no significant difference in terms of sex mismatch. As the patients were matched for transplantation period, there was no difference in immunosuppressive regimen.
Patients outcomes
During a median follow-up of 7.7 years, 16 patients died, 3 (21.5%) in PPCM group and 13 (46.5%) in control group. Mortality was significantly lower in PPCM group (p = 0.03, Figure 1). Causes of death are shown in Table 3. Major causes of one-year mortality after HT were rejection, hemorrhagic complications and infections; major causes of long-term mortality (> 1 year) after HT were rejection, CAV, and infections. Both early and late rejection rates were similar in both groups (p = 0.5 and 0.6 respectively). PPCM patients had a similar incidence of infections including cytomegalovirus (CMV) infections compared with control population (p = 0.07). Two patients from control group died within the first year following transplantation from septic shock, none in PPCM group. One more patient in control group died from septic shock > 1 year post transplant, none in PPCM group. PPCM patients had a similar risk of CAV compared with control group (p = 0.4). Pathological study of explanted hearts did not reveal any specific lesion.
Long-term survival after heart transplantation, PPCM group (PPCM (+)) and control patients (PPCM (-)). PPCM: peripartum cardiomyopathy.
Discussion
In this retrospective single-center study, we assessed post-transplant outcomes in a population of patients transplanted for severe HF in the setting of peripartum cardiomyopathy. Median follow-up was 7.7 years. We demonstrate upon our population that post-transplant mortality is significantly lower in patients transplanted for PPCM. Patients transplanted for PPCM did not display a significantly higher rate of transplant-related complications compared with control subjects matched for age and transplantation period.
Pre-transplant characteristics
In the pre-transplant setting, we significantly used more inotropes at the time of HT in PPCM patients compared with control subjects. The frequent need of medical intensive cardiovascular support in PPCM patients awaiting heart transplantation has also been demonstrated by others.1313 Rasmusson K, Brunisholz K, Budge D, Horne BD, Alharethi R, Folsom J, et al. Peripartum cardiomyopathy: post-transplant outcomes from the United Network for Organ Sharing Database. J Heart Lung Transplant. 2012;31(2):180-6. doi: 10.1016/j.healun.2011.11.018.
https://doi.org/10.1016/j.healun.2011.11...
Importantly, potential deleterious cellular alterations related to Dobutamine have recently been pointed in PPCM patients,2121 Stapel B, Kohlhaas M, Ricke-Hoch M, Haghikia A, Erschow S, Knuuti J, et al. Low STAT3 expression sensitizes to toxic effects of b-adrenergic receptor stimulation in peripartum cardiomyopathy. Eur Heart J. 2017;38(5):349-361. doi: 10.1093/eurheartj/ehw086.
https://doi.org/10.1093/eurheartj/ehw086...
and recent guidelines recommend a cautious use of inotropes for critically-ill PPCM patients.2222 Bauersachs J, Arrigo M, Hilfiker-Kleiner D, Veltmann C, Coats AJ, Crespo-Leiro MG, et al. Current management of patients with severe acute peripartum cardiomyopathy: practical guidance from the Heart Failure Association of the European Society of Cardiology Study Group on peripartum cardiomyopathy. Eur J Heart Fail. 2016;18(9):1096-105. doi: 10.1002/ejhf.586.
https://doi.org/10.1002/ejhf.586...
Data related to MCS in the management of PPCM patients are scarce.2323 Gevaert S, Van Belleghem Y, Bouchez S, Herck I, De Somer F, De Block Y, et al. Acute and critically ill peripartum cardiomyopathy and 'bridge to' therapeutic options: a single center experience with intra-aortic balloon pump, extracorporeal membrane oxygenation and continuous-flow left ventricular assist devices. Crit Care. 2011;15(2):R93. doi: 10.1186/cc10098.
https://doi.org/10.1186/cc10098...
,2424 Lueck S, Sindermann J, Martens S, Scherer M. Mechanical circulatory support for patients with peripartum cardiomyopathy. J Artif Organs. 2016;19(3):305-9. doi: 10.1007/s10047-016-0891-z.
https://doi.org/10.1007/s10047-016-0891-...
It seems however that MCS is an option for patients who deteriorate despite maximal therapy, in a strategy of bridge to transplantation or to recovery.66 McNamara DM, Elkayam U, Alharethi R, Damp J, Hsich E, Ewald G, et al; IPAC Investigators. Clinical outcomes for peripartum cardiomyopathy in North America: results of the IPAC Study (Investigations of Pregnancy-Associated Cardiomyopathy). J Am Coll Cardiol. 2015;66(8):905-14. doi: 10.1016/j.jacc.2015.06.1309.
https://doi.org/10.1016/j.jacc.2015.06.1...
,2222 Bauersachs J, Arrigo M, Hilfiker-Kleiner D, Veltmann C, Coats AJ, Crespo-Leiro MG, et al. Current management of patients with severe acute peripartum cardiomyopathy: practical guidance from the Heart Failure Association of the European Society of Cardiology Study Group on peripartum cardiomyopathy. Eur J Heart Fail. 2016;18(9):1096-105. doi: 10.1002/ejhf.586.
https://doi.org/10.1002/ejhf.586...
23 Gevaert S, Van Belleghem Y, Bouchez S, Herck I, De Somer F, De Block Y, et al. Acute and critically ill peripartum cardiomyopathy and 'bridge to' therapeutic options: a single center experience with intra-aortic balloon pump, extracorporeal membrane oxygenation and continuous-flow left ventricular assist devices. Crit Care. 2011;15(2):R93. doi: 10.1186/cc10098.
https://doi.org/10.1186/cc10098...
24 Lueck S, Sindermann J, Martens S, Scherer M. Mechanical circulatory support for patients with peripartum cardiomyopathy. J Artif Organs. 2016;19(3):305-9. doi: 10.1007/s10047-016-0891-z.
https://doi.org/10.1007/s10047-016-0891-...
-2525 Simon MA, Kormos RL, Murali S, Nair P, Heffernan M, Gorcsan J, et al. Myocardial recovery using ventricular assist devices: prevalence, clinical characteristics, and outcomes. Circulation. 2005;112(9 Suppl):I32-6. doi: 10.1161/CIRCULATIONAHA.104.524124.
https://doi.org/10.1161/CIRCULATIONAHA.1...
Noticeably, one major concern in the setting of long-term MCS in PPCM patients relates to a possibly higher risk of thrombotic complications in a prothrombotic condition such as the peripartum period.2626 Potapov EV, Loforte A, Weng Y, Jurmann M, Pasic M, Drews T, et al. Experience with over 1000 implanted ventricular assist devices. J Card Surg. 2008;23(3):185-94. doi: 10.1111/j.1540-8191.2008.00606.x.
https://doi.org/10.1111/j.1540-8191.2008...
Medical management of HF might be considered as non-optimal in our population, particularly among PPCM patients, as only one half received beta-blockers and ACE inhibitors. Importantly, under-treated patients were, in both groups, those requiring inotropic and mechanical circulatory support.
Seven percent (7%) of patients had CRT/ICD implantation. Recent data suggest that CRT is crucial in the management of PPCM patients presenting with persistent systolic dysfunction. It has indeed been demonstrated a rapid and significant LV recovery under CRT in PPCM patients with severe systolic dysfunction despite optimal medical therapy.2727 Mouquet F, Mostefa Kara M, Lamblin N, Coulon C, Langlois S, Marquie C, et al. Unexpected and rapid recovery of left ventricular function in patients with peripartum cardiomyopathy: impact of cardiac resynchronization therapy. Eur J Heart Fail. 2012;14(5):526-9. doi: 10.1093/eurjhf/hfs031.
https://doi.org/10.1093/eurjhf/hfs031...
Patients Outcomes after Heart Transplantation
We assessed post-transplant outcomes in patients transplanted for PPCM. Again, we demonstrated a significantly lower post-transplant all-cause mortality in patients transplanted for PPCM, with a similar rate of transplant-related complications as compared with control subjects. Data on long-term outcomes after HT for PPCM are contradictory, reporting either favorable outcomes,1111 Rickenbacher PR, Rizeq MN, Hunt SA, Billingham ME, Fowler MB. Long-term outcome after heart transplantation for peripartum cardiomyopathy. Am Heart J. 1994;127(5):1318-23. PMID: 8172060. or higher rejection rates and poorer outcomes.1212 Keogh A, Macdonald P, Spratt P, Marshman D, Larbalestier R, Kaan A. Outcome in peripartum cardiomyopathy after heart transplantation. J Heart Lung Transplant. 1994;13(2):202-7. PMID: 8031800.
13 Rasmusson K, Brunisholz K, Budge D, Horne BD, Alharethi R, Folsom J, et al. Peripartum cardiomyopathy: post-transplant outcomes from the United Network for Organ Sharing Database. J Heart Lung Transplant. 2012;31(2):180-6. doi: 10.1016/j.healun.2011.11.018.
https://doi.org/10.1016/j.healun.2011.11...
-1414 Rasmusson KD, Stehlik J, Brown RN, Renlund DG, Wagoner LE, Torre-Amione G, et al; Cardiac Transplant Research Database Group. Long-term outcomes of cardiac transplantation for peri-partum cardiomyopathy: a multiinstitutional analysis. J Heart Lung Transplant. 2007;26(11):1097-104. doi: 10.1016/j.healun.2007.08.002.
https://doi.org/10.1016/j.healun.2007.08...
Current practice is however favorable to HT for PPCM. As we did, a long-term survey of a small cohort of patients transplanted for PPCM has also shown favorable outcomes.2323 Gevaert S, Van Belleghem Y, Bouchez S, Herck I, De Somer F, De Block Y, et al. Acute and critically ill peripartum cardiomyopathy and 'bridge to' therapeutic options: a single center experience with intra-aortic balloon pump, extracorporeal membrane oxygenation and continuous-flow left ventricular assist devices. Crit Care. 2011;15(2):R93. doi: 10.1186/cc10098.
https://doi.org/10.1186/cc10098...
Limitations
The major limitation of our study is the small number of patients, prohibiting definitive conclusions. We arbitrarily adjudicated rejection in a binary way (present: yes, or no), which might therefore be considered as simplistic and of limited value.
Conclusion
We assessed long-term post-transplant outcomes in the setting of PPCM. Upon the studied population, we demonstrate a significantly lower long-term post-transplant mortality in patients transplanted for PPCM, with a similar rate of transplant-related complications as compared with control subjects. We show that heart transplantation for PPCM patients who did not significantly recover under maximal medical treatment remains appropriate. The overall impact of heart transplantation for PPCM is yet to be determined at a larger scale in well characterized population.
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Sources of FundingThere were no external funding sources for this study.
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Study AssociationThis study is not associated with any thesis or dissertation work.
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Ethics approval and consent to participateThis article does not contain any studies with human participants or animals performed by any of the authors.
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Publication Dates
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Publication in this collection
19 Feb 2018 -
Date of issue
Feb 2018
History
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Received
12 Mar 2017 -
Reviewed
02 Aug 2017 -
Accepted
29 Aug 2017