Pulmonary hypertension (PH) is a diverse disease defined by a mean pulmonary arterial pressure (mPAP) > 20 mmHg at rest using right heart catheterization[1] or by echocardiography with a right ventricular systolic pressure (RVSP) > 35 mmHg, absence of pulmonary stenosis and acute RHF, and usually accompanied by shortness of breath, fatigue, peripheral edema and other cardiovascular symptoms [2].
Globally 1% of the world population is affected by PH from which about 80% reside in underdeveloped nations where most patients with pulmonary hypertension are younger and frequently linked to chronic infection such as rheumatic heart disease, HIV and schistosomiasis, but they are not well studied [3].
Currently PH classified in to five groups based on pathophysiology[1]. Globally left side heart disease (including RHD) is the commonest cause of PH followed by lung disease, especially chronic obstructive lung disease[3]. Independent of the cause development of PH in these patients was associated with adverse outcomes and increased mortality[3].
Right heart catheterization is the gold standard for diagnosis and treatment decision of patients with pulmonary hypertension. However, its invasive as a result echocardiography is recommended as the first-line, non-invasive, diagnostic investigation in suspected PH [1]. Trans - thoracic echocardiography measures the systolic pulmonary arterial pressure (SPAP) with acceptable accuracy in rheumatic heart disease (RHD) patients [4].
RHD is a chronic sequalae of acute rheumatic fever. During 1990–2019, the global RHD prevalence have increased by 70.49% and reached 40.50 million in 2019. However, the death number due RHD was 0.31 million globally in 2019, with a decrease of 15.60% since 1990 [5]. Despite the global reduction in death due to RHD, it is important cause of cardiovascular death and disability in low and middle income regions, including Sub-Saharan Africa [6].
The REMEDY study showed most cases of newly diagnosed rheumatic heart disease patients present with advanced diseases and complications. Heart failure and pulmonary hypertension were the most commonly observed complications in many hospital-based studies [7].
The prevalence of pulmonary hypertension in RHD is variable since different studies use different tools to measure pulmonary hypertension. In Indian study which included 2005 patients with RHD from 2011–2016 showed PH prevalence to be 30.5%[8]. Similarly, in Iranian study using 558 RHD patients between 2007 and 2015, which defines significant PH as mean PAP > 40 mmHg, showed a prevalence of 27% [9].
A prospective study done in Saudi Arabia between 1989 and 2003 among 559 RHD patients who undergone MBV for severe MS, the prevalence of PASP > 50mmHg was 38%. The study also shows that the Doppler-monitored PASP fell to normal after 6–12 months of the intervention [10]. However, a study from south Yemen showed a high prevalence (80.4%) and most of it (60.1%) was from patients with mitral valve stenosis [11].
The epidemiology of PH in RHD is poorly understood in Africa despite the high incidence of PH risk factors, unique genetic backgrounds and lifestyles, and low access to healthcare[2]. A large multi centered prospective cross-sectional study called REMEDY study, which includes 3343 patients in 25 hospitals in 12 African countries (including Ethiopia), India and Yemen, between 2010 and 2012 showed that, the prevalence of PH in RHD was 28.8% [7]. Similarly, a study form Uganda showed a prevalence of 32.7% [12]. However, a study from Nigeria showed a high prevalence rate (72.1%) [13].
In Ethiopia, a study conducted in Saint Paul Hospital Millennium Medical College (SPHMMC) using 384 RHD patients in 2022, next to heart failure, pulmonary hypertension was the second most common complication that existed in 53.9% of patients [14]. Similarly, in a study conducted in Jimma (2019), including pediatric and adolescent RHD patients, PH was prevalent in 60.3% [15].
Several factors have been identified as associated with pulmonary hypertension development in RHD. For instance, in the REMEDY study using large sample size of RHD patients having moderate to severe mitral valve lesions and low income were found to be associated with PH [7]. In the Iranian study echocardiographic findings, absolute MVA, indexed MVA, and mean trans-mitral valve gradient were associated with the presence of PH [9].
Other factors identified in the literature associated with pulmonary hypertension development in RHD patients includes valvular intervention [16, 17], only diuretics usage [18], long duration of disease [19], raised filling pressures, LV systolic dysfunction, LV dilation [20] and low income[7].
This study tried to fill the epidemiologic data gaps regarding PH-RHD and its associated factors in one of the Sub-Saharan countries, where the prevalence of RHD is high.