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Comparison of the effect of sildenafil and tadalafil on pulmonary hypertension associated with hemodynamically significant pdas treatment of pulmonary hypertension in HS-PDA patients

Ali Mazouri , Mohammad Radgoodarzi , Zeinab Zohrevandi, Sahar Hemmati , Pegah Taherifard

Journal of Pharmaceutical Negative Results, 2022

96 participants

Abstract

Objective: Treating the hemodynamically significant patent ductus arteriosus (hs-PDA) includes conservative therapy besides using non-steroidal anti-inflammatory drugs (NSAIDs) and acetaminophen. In addition, the pulmonary arterial pressure increases in hs-PDA. It is not clear whether the drugs used in acute pulmonary arterial hypertension (PAH) can improve the hs-PDA or not. This study evaluates the effect of anti-PAH drugs, sildenafil and tadalafil on patients with hs-PDA and PAH.Methods: Neonates with hs-PDA and PAH diagnosis are included in this triple-blinded clinical randomized trial study. The patients are assigned to group A (tadalafil + acetaminophen), B (sildenafil + acetaminophen), and C (acetaminophen alone). The patients were evaluated by their echocardiography findings, before and after therapy. Results: Overall, 96 patients were included in this study, 32 for each group. The patients were match for all of the demographic data. All patients had improved echocardiography parameters, except for the TAPSE and MPA diameter for tadalafil patients. On the other hand, the RVEDd and RVESd were improved better in tadalafil patients, in comparison with the sildenafil group (p = 0.012 and 0.022, respectively). There was no significant difference in other echocardiography parameters or the adverse effects. Conclusions: Using anti-PAH drugs such as tadalafil and sildenafil to hs-PDA patients with PAH does not have additional effect to the acetaminophen. Tadalafil and…

How strong is the evidence?

Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 2 of 5 (High · randomized trial). Randomized trials of a reasonable size are the strongest single-study design. Reported size: 96 participants or records.

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