Abstract
Rheumatic heart disease (RHD) remains a global health burden. In 2017, approximately 38–40.8
million cases of RHD were observed all around the world. The prevalence of RHD in non-endemic
regions is 3.4 cases per 100,000, whereas in endemic regions, it is higher than 1,000 cases per
100,000. RHD is also responsible for the
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premature deaths of 0.15/100000 children and an annual
case-fatality rate of 1.5% per year among the global population ages. In Indonesia, eighty-three
out of 15,608 mine workers in Papua suffered from RHD. A cardiac center in Bandung observed
that 108/4,682 (2.3%) of the patients were diagnosed with RHD. Meanwhile, the Cardiovascular
Centre Harapan Kita, Jakarta, a national cardiovascular disease referral hospital in Indonesia,
stated that 40.5% of 7112 valvular cases during 2016–2019 were RHD cases. Definitive
management of RHD with significant mitral valve stenosis consist of percutaneous balloon mitral
valvuloplasty (PBMV) and mitral valve surgery (MVS). The survival analysis of patient with
rheumatic MS after PBMV compared to MVS in Indonesia revealed that those who underwent
PBMV, 1.8% died within 24 months, while 3.5% of those who underwent mitral valve replacement
died within 27 months. The occurrence of rehospitalization did not differ between the two groups,
with acute decompensated heart failure being the leading cause. PBMV is the first choice for
patients with rheumatic heart disease without contraindications because it provides faster relief
compared to mitral valve replacement. In terms of cost, PBMV is more affordable and less
invasive, which is more beneficial for patients with rheumatic heart disease in low- to middleincome countries. Thereafter, a cohort retrospective study was conducted to assess the
improvement of exercise capacity after early phase II cardiac rehabilitation in patients who
undergo rheumatic mitral valve surgery. The study revealed that 6MWD and VO2 peak increased
significantly in these patients after the early phase II CR program (p = 0.001). On the other hand,
the use of ACE inhibitors as anti-fibrotic treatment is now being considered to address the fibrotic
process in rheumatic mitral stenosis valve as a non-intervention management. It has been
demonstrated that ACE inhibitors can break the inflammatory cycle that leads to fibrosis in the
valve. Thus, we developed a research protocol to determine the anti-fibrotic effects of ACEI and
designed an RCT in which patients received ramipril (5 mg) for at least 3 months preoperatively.
Ramipril 5mg could be a breakthrough in the management of rheumatic heart disease, improving
patient outcomes and proving highly beneficial in low- to middle-income countries. In conclusion,
rheumatic heart disease, specifically rheumatic mitral stenosis, is the most common valvular
disorder that occurs and should be comprehensively addressed through primary prevention,
secondary prevention, non-intervention management, intervention management, and
rehabilitation. Each approach is valuable and helpful in providing advancements in the
management of rheumatic mitral stenosis.
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