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|Clinical and hemodynamic effect of endothelin receptor antagonists in eisenmenger syndrome
Emir Yonas1, Raymond Pranata2, Muhammad Yamin3, Nuvi Nusarintowati4, Siti Elkana Nauli4, Hafil Budianto Abdulgani5, Bambang Budi Siswanto6
1 Faculty of Medicine, Universitas YARSI, Jakarta, Indonesia
2 Faculty of Medicine, Universitas Pelita Harapan, Banten, Indonesia
3 Division of Cardiology, Department of Internal Medicine, Faculty of Medicine, Universitas Indonesia/ Cipto Mangunkusumo National General Hospital, Jakarta, Indonesia
4 Department of Cardiology and Vascular Medicine, Tangerang District Hospital, Tangerang. Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia
5 Department of Cardiothoracic Surgery, Medika Permata Hijau Hospital, Jakarta, Indonesia
6 Department of Cardiology and Vascular Medicine, Faculty of Medicine Universitas Indonesia, National Cardiovascular Center Harapan Kita, Jakarta, Indonesia
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|Date of Submission||29-Nov-2019|
|Date of Decision||17-Mar-2020|
|Date of Acceptance||06-May-2020|
|Date of Web Publication||24-Jul-2020|
| Abstract|| |
Introduction: Endothelin receptor antagonists (ERAs) are widely accepted as a specific treatment for pulmonary arterial hypertension. Unfortunately, consensus and recommendations are lacking for the treatment of patients who suffer from pulmonary arterial hypertension and congenital heart disease, including Eisenmenger syndrome.
Objective: This meta-analysis aimed to compare the effect of ERA on patients with Eisenmenger syndrome.
Methods: Electronic search on PubMed (MEDLINE), EBSCO, EuropePMC, Clinicaltrials.gov, and Google Scholar was done. Studies involving the use of ERAs on Eisenmenger syndrome patients were included. There were 18 studies included. The primary outcome of interest was the 6-min walking test distance before and after exposure to ERA.
Results: There were 517 patients with Eisenmenger syndrome. The subjects had Eisenmenger syndrome secondary to congenital heart disorders, with WHO functional Class ranging from Class I–IV. The follow-up ranges from a mean of 4–60 months. Seventeen studies reported a statistically significant difference between pretreatment and the posttreatment result of 6-min walking test distance. Pooled mean difference comparing pre and posttreatment values yielded an increase of 55.24 m (42.15, 68.33) P < 0.001; moderate heterogeneity I2 51% P = 0.008. Pooled mean pulmonary vascular resistance index difference comparing pre and posttreatment values yielded a decrease of 4.76 woods unit (-6.86, -2.66), P < 0.001 favoring posttreatment; low heterogeneity I2 0%, P = 0.82. Pooled mean mean pulmonary arterial pressure difference comparing pre and posttreatment values yielded a decrease of 5.40 mmHg (-7.53, -3.28), P < 0.001 favoring posttreatment, low heterogeneity I2 0%, P = 0.65.
Conclusion: Implementation of ERA in Eisenmenger improves 6-min walking distance and pulmonary vascular pressure indices. Earlier administration of ERA might be beneficial, further studies are needed to assess mortality benefit of this agent.
Keywords: Adult, congenital heart disease, Eisenmenger syndrome, endothelin receptor antagonist
|How to cite this URL:|
Yonas E, Pranata R, Yamin M, Nusarintowati N, Nauli SE, Abdulgani HB, Siswanto BB. Clinical and hemodynamic effect of endothelin receptor antagonists in eisenmenger syndrome. Ann Pediatr Card [Epub ahead of print] [cited 2020 Aug 14]. Available from: http://www.annalspc.com/preprintarticle.asp?id=290592
| Introduction|| |
Endothelin receptor antagonists (ERAs) are widely accepted as a specific treatment for pulmonary arterial hypertension. Unfortunately, consensus and recommendations are lacking for the treatment of patients that suffers from pulmonary arterial hypertension and congenital heart disease, including Eisenmenger syndromr as the possible consequence of uncorrected or suboptimal correction of congenital heart diseases. This lack of consensus arises from the limited data that is available on the efficacy of specific therapies for patients with pulmonary hypertension secondary to congenital heart disease (PH-CHD) and patients with Eisenmenger syndrome.
It is important to note that currently, there has been no established relation between PH-specific therapy and survival of patients with PH-CHD and Eisenmenger syndrome.
Several widely known trial such as the MAESTRO and BREATHE-5 trial have been conducted that studies specific subjects with Eisenmenger syndrome and the subsequent changes in hemodynamic and clinical profiles with the use of ERA agents, with the majority of studies using bosentan, with macitentan and sitaxentan to a lesser degree.,
This meta-analysis aims to pool results across studies that involve the use of ERAs on patients with Eisenmenger syndrome. The authors hoped that with the availability of these pooled results, a thorough analysis could be synthesized in this topic.
| Methods|| |
We performed a comprehensive search on studies that assess the use of ERAs in Eisenmenger syndrome patients from inception up until January 2020. We searched (Endothelin receptor antagonist Eisenmenger syndrome) and its synonyms using PubMed, EuropePMC, EBSCOhost, Cochrane Central Database, ClinicalTrials. gov, and snowballing from potential articles cited by other studies. The records were then systematically evaluated using inclusion and exclusion criteria. Two researchers (E. Y and R. P) independently performed an initial search; discrepancies were resolved by discussion.(A preferred reporting items for systematic reviews and Meta-Analysis flowchart of the literature search strategy of studies).
The inclusion criteria for the study are all studies that assess the use of ERAs on Eisenmenger syndrome patients. Cross-sectional and case–control studies were excluded as of those studies with insufficient data to assess the outcome of interest. The primary outcome measured was the 6 min walking test distance (6MWD). Secondary outcomes were Borg dyspnea index, resting oxygen saturation, liver function test results, and pulmonary vascular resistance index. We include all clinical researches/original articles and exclude case reports, review articles, and non-English language articles.
Data extraction and risk of bias assessment were done by two independent authors (E. Y and R. P) using standardized extraction form with includes authors, year of publication, study design, sample size, type of ablation, and length of follow-up.
Meta-analysis was performed using RevMan version 5.3 Software (Cochrane Collaboration). We used mean difference (MD) and its standard deviation (SD) as a pooled measure for the continuous data. Inconsistency index (I2) test, which ranges from 0% to 100% was used to assess heterogeneity across studies. A value >50% or P < 0.05 indicates statistically significant heterogeneity. We used the generic inverse variance method (for HR and MD) with a fixed-effect model for meta-analysis and a random-effect model in case of significant heterogeneity. All P values were two-tailed with a statistical significance set at 0.05 or below.
| Results|| |
The search result for studies that involve the use of ERA on Eisenmenger patients yielded a total of potential 298 articles. We removed 197 duplicates. We excluded 72 articles after screening the titles and abstracts. There were 29 potentially relevant articles. We screened the full articles and abstracts and after applying the inclusion and exclusion criteria, 11 studies were excluded because studies did not include outcome of interest (n = 7), studies being meta-analysis (n = 2), studies being systematic review (n = 1), studies comparing between ERA to another agent (n = 1). We included 18 studies for qualitative synthesis and 18 studies were available for meta-analysis. There were 517 patients with Eisenmenger who were administered ERA from these studies. All subjects suffered from Eisenmenger syndrome secondary to congenital heart diseases. The follow-up ranges from 4–60 months [Table 1] and [Figure 1].
Six minutes walking test distance
Seventeen studies reported a statistically significant difference in walking distance between posttreatment and pretreatment with ERAs. Pooled MD comparing pre and posttreatment values yielded an increase of 55.24 m (42.15, 68.33) P < 0.001; moderate heterogeneity I2 51% P = 0.008. We performed sensitivity analysis and upon removal of study by Gatzoulis et al. 2019, Kermeen et al. 2010 and Zuckerman et al. 2011 heterogeneity decreased to I2 0% P = 0.46. with a pooled result of 54.67 m (44.80, 64.55) P < 0.001 [Figure 2]a and [Figure 2]b.,,,,,,,,,,,,,,,,
|Figure 2: Meta analysis. (a) 6 min walking distance, pooled mean difference (meters) favoring posttreatment. (b) Funnel plot of analysis|
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Borg dyspnea index
Seven studies reported a statistically significant difference in Borg dyspnea index between posttreatment and pretreatment with ERAs. Pooled MD comparing pre and posttreatment values yielded a decrease of 0.99 Borg dyspnea index [−1.43, −0.54], P < 0.001 favoring posttreatment; low-moderate heterogeneity I2 42%, P = 0.11.,,,,,,
We performed sensitivity analysis and upon removal of the study by Baptista et al. and D'alto et al. (2012). Heterogeneity decreased to I2 0% P = 0.51 [Figure 3].
|Figure 3: Borg dyspnea index, pooled mean difference favoring posttreatment|
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Resting oxygen saturation
Fifteen studies reported a statistically significant difference in resting oxygen saturation between posttreatment and pretreatment with ERAs. Pooled MD comparing pre and posttreatment values yielded an increase of 1.93% (0.75, 3.11), P < 0.001 favoring posttreatment; moderate heterogeneity I2 57%, P = 0.003. Sensitivity analyses were performed and removal of the study by Crepaz et al. D'Alto et al. (2007) Gallie et al. and Kermeen et al. 2010 resulted in a pooled MD of 1.93% (1.02, 2.84) P < 0.001; I2 0% P = 0.53 [Figure 4]a and [Figure 4]b.,,,,,,,,,,,,,,
|Figure 4: (a) Resting saturation of oxygen, pooled mean difference (%) favoring posttreatment. (b) Funnel plot of analysis|
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Pulmonary vascular resistance index
Six studies reported a statistically significant difference in pulmonary vascular resistance index between posttreatment and pretreatment with ERAs. Pooled MD comparing pre and posttreatment values yielded a decrease of 4.76 Woods unit (−6.86, −2.66), P < 0.001 favoring posttreatment; low heterogeneity I2 0%, P = 0.82 [Figure 5].,,,,,
|Figure 5: Pulmonary vascular resistance index, pooled mean difference (woods unit) favoring Posttreatment|
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Mean pulmonary arterial pressure
Nine studies reported a statistically significant difference in mean pulmonary arterial pressure (MPAP) between posttreatment and pretreatment with ERAs. Pooled MD comparing pre- and post-treatment values yielded a decrease of 5.40 mmHg (−7.53, −3.28), P < 0.001 favoring posttreatment, low heterogeneity I2 0%, P = 0.65 [Figure 6].,,,,,,,
|Figure 6: Mean pulmonary arterial pressure, pooled mean difference (mmHg) favoring posttreatment|
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Aspartate aminotransferase levels
We performed a meta-analysis comparing aspartate aminotransferase levels in patients who received ERAs before and after treatment with ERAs. The pooled MD yielded an increase of 0.69 U/L (−1.23, 2.61), P = 0.48, low-moderate heterogeneity I2 29%, P = 0.22. However, these results were not statistically significant.,,,,,
Alanine aminotransferase levels
We performed a meta-analysis comparing alanine aminotransferase levels in patients who received ERAs before and after treatment with ERAs. The pooled MD yielded an increase of 1.81 U/L (−0.42, 4.05), P = 0.11, low heterogeneity I2 0%, P = 0.74. However, these results were not statistically significant.,,,,,,
We performed subgroup analysis on 6MWD and pulmonary vascular resistance index (PVRI) based on follow-up length (short-term ≤ 6 months and long-term ± 24 months).
Six minutes walking distance, short-term follow-up
Seven Studies reported a statistically significant difference in walking distance between posttreatment and pretreatment with ERAs. Pooled MD comparing pre and posttreatment values yielded an increase of 44.96 m (31.31, 58.62) P < 0.001; low-moderate heterogeneity I2 32% P = 0.19.,,,,,,
Six minutes walking distance, long-term follow-up
Eight studies reported a statistically significant difference in walking distance between posttreatment and pretreatment with ERAs. Pooled MD comparing pre and posttreatment values yielded an increase of 72.96 m (54.57, 91.34) P < 0.001; low heterogeneity I2 20% P = 0.27.,,,,,,,
Pulmonary vascular resistance index, short-term follow-up
Three studies reported a statistically significant difference in pulmonary vascular resistance index between posttreatment and pretreatment with ERAs. Pooled MD comparing pre and posttreatment values yielded a decrease of 4.81 Woods unit (−7.64, −1.97), P < 0.001 favoring posttreatment; low heterogeneity I2 0%, P = 0.94.,,
Pulmonary vascular resistance index, long term follow up
Three studies reported a statistically significant difference in pulmonary vascular resistance index between posttreatment and pretreatment with ERAs. Pooled MD comparing pre and posttreatment values yielded a decrease of 4.70 Woods unit (−7.82, −1.58), P = 0.003 favoring posttreatment; low heterogeneity I2 4%, P = 0.35.,,
| Discussion|| |
Our study showed that the use of ERAs significantly increases 6MWD of patients. In normal patients, a result of 400–700 m is achievable, this is contrasted with the pretreatment levels of patients in this meta-analysis, in which only 1 of 15 studies showed a pretreatment 6MWD higher than 400 m.,
We observed a MD of 55.24 m in between posttreatment and pretreatment results of 6MWD. This is in accordance with data from several studies that stated that in the light of available evidence, a minimally important difference in changes on 6MWD should be no less than 30 m.
Due to the diversity of follow-up length of studies included in this meta-analysis, we performed a subgroup analysis on 6MWD and PVRI based on short term (≤6 months) and long-term (±24 months) to further observe the effect of ERA in eisenmenger patients and to avoid bias from synthesizing conclusion from such diverse length of follow up. The result of this subgroup analysis on 6MWD on both short and long term follow up shows that the use of ERA is associated with a longer posttreatment 6MWD (44.96 and 72.96 m MD, respectively). A similar result was also observed on a subgroup analysis of PVRI on short and long term follow-up showing that the use of ERA is associated with decreased posttreatment level of PVRI (4.81 vs. 4.70 woods unit MD, respectively).
Patients with Eisenmenger syndrome commonly suffer from dyspnea that hinders them from performing daily routines, a quantitative decrease of dyspnea can be observed by the decrease of mean Borg dyspnea index that can be observed in this meta-analysis, a cumulative decrease of Borg dyspnea index rating of 00.99 points can be observed on this meta-analysis. However, this kind of dyspnea scoring poses a risk of subjectivity due to these scores being rated by the patient on a subjective basis.
We did not observe a significant improvement in resting oxygen saturation even with treatment using ERAs, with only an increase of 1.93% in pooled results. However, we observed a significant decrease in pulmonary vascular resistance index of 4.76 woods unit in pooled results after treatment with ERA.
PVRI is thought to be the direct indices of pulmonary vascular resistance, and its decrease following treatment with ERA signifies the potential benefit of using this agent on Eisenmenger syndrome patients.
Furthermore, a cumulative decrease of mean Pulmonary artery pressure was also observed with an observed mean reduction of 5.40 mmHg after treatment with ERA.
Elevations in liver function test and subsequent hepatic injury are some major concerns in regards to treatment with ERA, in this meta-analysis, we did not find any significant alteration of liver function test in the studies that are included in this meta-analysis, a pooled result of changes in Aspartate transaminase and Alanine Transaminase showed only minimal alterations after treatment with ERA, however, this analysis were not statistically significant and further studies will need to be done.
Our initial meta-analysis on resting oxygen saturation showed a low-moderate heterogeneity of 57% with P = 0.001. Based on the approach suggested by Fletcher, this meta-analysis was comprised of studies that are mostly prospective cohort. This study only showed a low-moderate heterogeneity. The forest plot of this meta-analysis showed the consistent result of a trend of decrease in resting saturation of oxygen. The sensitivity analysis of this meta-analysis does not show a significant change in the exclusion of said studies.
In this meta-analysis, we can observe improvement in the 4th month after the administration of ERA. This is due most studies performing first follow-up at the 4th month since the initial administration of ERA. Clinical improvement consists of improvement in 6-min walking distance and Borg dyspnea index while hemodynamic improvement consists of improvement in MPAP, pulmonary vascular resistance index and resting saturation of oxygen.
The observed improvement after treatment with ERAs on this meta-analysis showed that the use of ERAs in Eisenmenger syndrome patients is highly likely to be beneficial to patients.
The rationale and support for the use of Bosentan in Eisenmenger syndrome came from the BREATHE-5 study, in which 54 treatment naïve patients with WHO FC III was assigned to Bosentan or placebo. 6MWD significantly improved, PVR was reduced by a 5.9 woods unit., and MPAP was reduced by 5.5 mmHg. However, the result two of major randomized control trials, namely MAESTRO and BREATHE-5, were conflicting in terms that in MAESTRO study which compared between macitentan and placebo on patients >12 years old with congenital cardiac defects, 6MWD was not significantly improved in the macitentan versus placebo (18.3 m vs. 19.7 m in the placebo group). Unexpectedly, large improvement in 6MWD in the placebo group was observed. However, it is to be taken into consideration that the MAESTRO trial included a more heterogeneous study population than the BREATHE-5 Trial., Currently, the statement of AHA/ACC on the 2018 AHA/ACC Guideline for the Management of Adults with Congenital Heart Disease stated that Bosentan is beneficial in symptomatic adults with Eisenmenger syndrome with ASD or VSD (recommendation Class I, level of Evidence A). In symptomatic adults with Eisenmenger syndrome, bosentan and PDE-5 inhibitors are reasonable in combination if symptomatic improvement does not occur with either medication alone (Recommendation Class IIa, Level of Evidence B-R [Moderate quality evidence from 1 or more RCTs/Meta-analyses of moderate quality RCTs]). Regarding Eisenmenger syndrome with ASD/VSD shunt, Bosentan is reasonable therapy to treat symptomatic adults with Eisenmenger syndrome with 1 of the following: Shunts other than ASD/VSD (PDA, aortopulmonary window) (Level of Evidence C-EO) or Complex congenital heart lesions (Level of Evidence B-NR).
In comparison with the AHA/ACC guideline, the ESC guideline stated that the ERA bosentan should be initiated in WHO-FC III patients with Eisenmenger syndrome (Recommendation Class I, Level of Evidence B). Combination therapy may be considered in WHO-FC III patients with Eisenmenger Syndrome (Recommendation Class IIb, Level of Evidence C). Regarding other agents of pulmonary hypertension-specific therapy, ESC stated that Other ERAs, phosphodiesterase type-5 Inhibitors and prostanoids should be considered in WHO-FC III patients with Eisenmenger syndrome.(recommendation Class IIa, Level of Evidence C). The ESC guideline also highlights explicitly that currently there is only one randomized control trial including 54 patients that has a favorable effect on exercise capacity and hemodynamics of ERA treatment on Eisenmenger syndrome (BREATHE-5 Study).
The results of this meta-analysis further solidify the latest recommendation of AHA/ACC and ESC regarding the use of ERA in Eisenmenger syndrome patients, that the use of these agents is beneficial. Despite the unavailability of data regarding the survival of patients on ERA, results of hemodynamic measurements showed significant improvement with the use of these agents. However, further studies will be needed to obtain data regarding mortality while on ERA treatment, and comparison of performance between ERA and other agents in Eisenmenger syndrome patients. Data regarding mortality benefit on ERA is crucial to determine whether earlier administration of ERA in Eisenmenger patients (WHO FC less than III) or even patients with early symptomatic pulmonary hypertension will be beneficial, as compared to ESC guideline in which ERA will only be considered in Eisenmenger patients with WHO FC III. Based on the hemodynamic improvements with the use of ERA, the authors of this meta-analysis postulated that earlier administration of ERA will be beneficial, however, further mortality data will be needed.
With the current guidelines mainly focusing on the BREATHE-5 Study which generated a favorable outcome in using ERA in Eisenmenger patients, the authors of this meta-analysis would like to bring a broader perspective using multiple other studies on the hemodynamic and clinical profile of patients who are exposed to ERA.
As per the recommendations from Cochrane collaborations, the authors of this manuscript utilizes the I2 method of projecting statistical heterogeneity on this meta-analysis. We performed a sensitivity analysis on results that are deemed to have significant heterogeneity. According to available literature, we classified heterogeneity to No observed heterogeneity, low, moderate, and high based on percentages (0, 25, 50, and 75% respectively). We also performed sensitivity analysis based on the P value of heterogeneity quantification, and we performed a further sensitivity analysis on P value that exceeds P = 0.1 on heterogeneity quantification. Due to the heterogeneity of methods of studies and data gathering, we are unable to include the World Health Organization functional class (WHO-FC) on our meta-analysis; however, we can observe that improvement occurs on patients that consume ERA on WHO FC II–IV. With patients being reclassified into milder functional classes at the end of studies.
The authors acknowledged that, based on the current data, we cannot establish a mortality benefit based on the use of ERA agents due to the lack of survival data. We observed improvement in clinical and hemodynamic parameters after treatment with ERA; however, these findings did not directly translate into mortality benefit of using ERA agents. In future, more randomized control trials and longer follow-up of these patients are needed to better understand the potential benefit, mortality benefit, and safety profile of ERAs in Eisenmenger syndrome. The limitation of this systematic review includes potential selection bias because not all of the studies included were randomized controlled trials. The majority of studies included in this meta-analysis only contain pre and posttreatment data of patients without control and no data regarding survival. Based on our analysis using funnel plots, we cannot exclude the possibility of publication bias on analysis regarding resting oxygen saturation. The study also included studies with varying lengths of follow-up and treatment using ERA. Ideally, it is prudent to perform an analysis of studies with the longest follow-ups, however, due to the sparse nature of data regarding ERA in Eisenmenger patients, such an ideal approach was not applicable.
| Conclusion|| |
Administration of ERA on patients with Eisenmenger showed promising results in terms of 6-min walking distance, pulmonary vascular resistance index and MPAP. ERA also decreases the Borg dyspnea index in patients with Eisenmenger syndrome. Randomized Control trials should be done in the future to better compare the treatment effects of this agent. A longer follows-up period is needed to better understand mortality benefit and safety profile of this agent. We also suggest that future studies include all of the parameters studied in this meta-analysis.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Gatzoulis MA, Landzberg M, Beghetti M, Berger RM, Efficace M, Gesang S, et al
. Evaluation of macitentan in patients with eisenmenger syndrome. Circulation 2019;139:51-63.
Gatzoulis MA, Beghetti M, Galiè N, Granton J, Berger RM, Lauer A, et al
. Longer-term bosentan therapy improves functional capacity in Eisenmenger syndrome: Results of the BREATHE-5 open-label extension study. Int J Cardiol 2008;127:27-32.
Kaya MG, Lam YY, Erer B, Ayhan S, Vatankulu MA, Nurkalem Z, et al
. Long-term effect of bosentan therapy on cardiac function and symptomatic benefits in adult patients with Eisenmenger syndrome. J Card Fail 2012;18:379-84.
Kermeen FD, Franks C, O'Brien K, Seale H, Hall K, McNeil K, et al
. Endothelin receptor antagonists are an effective long term treatment option in pulmonary arterial hypertension associated with congenital heart disease with or without trisomy 21. Heart Lung Circ 2010;19:595-600.
Kotlyar E, Sy R, Keogh AM, Kermeen F, Macdonald PS, Hayward CS, et al
. Bosentan for the treatment of pulmonary arterial hypertension associated with congenital cardiac disease. Cardiol Young 2006;16:268-74.
Mehta PK, Simpson L, Lee EK, Lyle TA, McConnell ME, Book WM. Endothelin receptor antagonists improve exercise tolerance and oxygen saturations in patients with Eisenmenger syndrome and congenital heart defects. Texas Hear Inst J 2008;35:256-61.
Schulze-Neick I, Gilbert N, Ewert R, Witt C, Gruenig E, Enke B, et al
. Adult patients with congenital heart disease and pulmonary arterial hypertension:First open prospective multicenter study of bosentan therapy. Am Heart J 2005;150:716.
Serino G, Guazzi M, Micheletti A, Lombardi C, Danesi R, Negura D, et al
. Effect of bosentan on exercise capacity and clinical worsening in patients with dual down and eisenmenger syndrome. Clin Med Insights Cardiol 2013;7:29-34.
Zuckerman WA, Leaderer D, Rowan CA, Mituniewicz JD, Rosenzweig EB. Ambrisentan for pulmonary arterial hypertension due to congenital heart disease. Am J Cardiol 2011;107:1381-5.
Abd El Rahman MY, Rentzsch A, Scherber P, Mebus S, Miera O, Balling G, et al
. Effect of bosentan therapy on ventricular and atrial function in adults with Eisenmenger syndrome. A prospective, multicenter study using conventional and Speckle tracking echocardiography. Clin Res Cardiol 2014;103:701-10.
Apostolopoulou SC, Manginas A, Cokkinos DV, Rammos S. Long-term oral bosentan treatment in patients with pulmonary arterial hypertension related to congenital heart disease: A 2-year study. Heart 2007;93:350-4.
Baptista R, Castro G, da Silva AM, Monteiro P, Providência LA. Long-term effect of bosentan in pulmonary hypertension associated with complex congenital heart disease. Rev Port Cardiol 2013;32:123-9.
Crepaz R, Romeo C, Montanaro D, De Santis S. Long-term results of treatment with bosentan in adult Eisenmenger's syndrome patients with Down's syndrome related to congenital heart disease. BMC Cardiovasc Disord 2013;13:74.
D'Alto M, Vizza CD, Romeo E, Badagliacca R, Santoro G, Poscia R, et al
. Long term effects of bosentan treatment in adult patients with pulmonary arterial hypertension related to congenital heart disease (Eisenmenger physiology): Safety, tolerability, clinical, and haemodynamic effect. Heart 2007;93:621-5.
D'Alto M, Romeo E, Argiento P, Sarubbi B, Santoro G, Grimaldi N, et al
. Bosentan–sildenafil association in patients with congenital heart disease-related pulmonary arterial hypertension and Eisenmenger physiology. Int J Cardiol 2012;155:378-82.
Diller GP, Dimopoulos K, Kaya MG, Harries C, Uebing A, Li W, et al
. Long-term safety, tolerability and efficacy of bosentan in adults with pulmonary arterial hypertension associated with congenital heart disease. Heart 2007;93:974-6.
Galiè N, Beghetti M, Gatzoulis MA, Granton J, Berger RM, Lauer A, et al
. Bosentan therapy in patients with eisenmenger syndrome. Circulation 2006;114:48-54.
Taçoy G, Başer HD, Türkoǧlu S, Cengel A. The management of adult female patients with Eisenmenger syndrome and advanced pulmonary arterial hypertension treatment: Single center experience and follow-up for 5 years. Turk Kardiyol Dern Ars 2014;42:531-41.
Casanova C, Celli BR, Barria P, Casas A, Cote C, de Torres JP, et al
. The 6-min walk distance in healthy subjects: Reference standards from seven countries. Eur Respir J 2011;37:150-6.
Mathai SC, Puhan MA, Lam D, Wise RA. The minimal important difference in the 6-minute walk test for patients with pulmonary arterial hypertension. Am J Respir Crit Care Med 2012;186:428-33.
Fletcher J. What is heterogeneity and is it important? BMJ 2007;334:94-6.
Stout KK, Daniels CJ, Aboulhosn JA, Bozkurt B, Broberg CS, Colman JM, et al
. 2018 AHA/ACC guideline for the management of adults with congenital heart disease: A report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation 2019;139:e698-800.
Baumgartner H, Bonhoeffer P, De Groot NM, de Haan F, Deanfield JE, Galie N, et al
. ESC Guidelines for the management of grown-up congenital heart disease (new version 2010): The task force on the management of grown-up congenital heart disease of the European Society of Cardiology (ESC). Eur Heart J 2010;31:2915-57.
Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. BMJ 2003;327:557-60.
Faculty of Medicine, Universitas YARSI, Jl. Letjend Suprapto No. 1, RW. 5, Cemp. Putih Timur, Daerah Khusus Ibukota Jakarta 10510
Source of Support: None, Conflict of Interest: None
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 6], [Figure 5]