Assessment of exercise tolerance using cardiopulmonary exercise test in patients with chronic obstructive pulmonary disease and secondary pulmonary arterial hypertension treated with Sildenafil versus those receiving only standard-of-care

Darwish Ibrahim Darwish, Yasser Moustafa, Hossam M. Abdel-Hamid, Rehab M. Mohammed
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Abstract

Pulmonary arterial hypertension (PAH) is a common complication of chronic obstructive pulmonary disease (COPD), which can lead to shorter survival and poor clinical outcomes. Patients suffering from PAH display a cardiopulmonary exercise testing (CPET) profile with several atypical factors, such as decreased work rate, limited ability to do aerobic activities, and ventilatory insufficiency. To assess and compare exercise tolerance by CPET in COPD patients with secondary PAH receiving cGMP-specific phosphodiesterase type-5 (PDE-5) inhibitor (sildenafil) versus those who are receiving standard-of-care only. This is a prospective, cross-sectional research in which a total of 30 COPD patients with mild to severe obstruction and secondary PAH were recruited; all patients were treated with standard-of-care treatment for COPD; moreover, half of the recruited patients were also on sildenafil 60 mg/day for at least 3 months at the time of recruitment (sildenafil users) as specific therapy for PAH while the other half were not (non-users). All patients underwent CPET to assess their exercise capacity. No significant statistical differences were observed between sildenafil users and non-users in all CPET parameters except in respiratory exchange ratio (RER) during both exercise and recovery with sildenafil users showing a lower RER in both phases compared to non-users (p = 0.02, 0.01, respectively). Also, resting diastolic blood pressure (DBP) was significantly lower in sildenafil users (p = 0.02). In addition, sildenafil users did not exhibit significant differences compared to non-users in terms of Modified Medical Research Council (mMRC) score, COPD assessment test (CAT) score, or spirometric parameters. Our findings suggest that there were no significant differences in overall exercise capacity, nor in symptoms or spirometric parameters between COPD patients with secondary PAH receiving sildenafil and those who were not.
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使用西地那非治疗慢性阻塞性肺病和继发性肺动脉高压患者与仅接受标准治疗者的心肺运动测试评估运动耐量
肺动脉高压(PAH)是慢性阻塞性肺疾病(COPD)的常见并发症,可导致患者存活期缩短和临床疗效不佳。PAH 患者在心肺运动测试(CPET)中表现出一些非典型因素,如工作率下降、有氧活动能力受限和通气不足。通过 CPET 评估和比较接受 cGMP 特异性 5 型磷酸二酯酶(PDE-5)抑制剂(西地那非)治疗的继发性 PAH COPD 患者与仅接受标准治疗的患者的运动耐量。这是一项前瞻性横断面研究,共招募了 30 名患有轻度至重度阻塞和继发性 PAH 的慢性阻塞性肺疾病患者;所有患者都接受了慢性阻塞性肺疾病的标准护理治疗;此外,招募时有一半患者还在接受西地那非 60 毫克/天的治疗,持续时间至少 3 个月(西地那非使用者),作为 PAH 的特殊疗法,而另一半患者则没有接受治疗(非使用者)。所有患者都接受了 CPET 测试,以评估他们的运动能力。在所有 CPET 参数中,西地那非使用者和非使用者之间均未观察到明显的统计学差异,但在运动和恢复期的呼吸交换比(RER)方面除外,与非使用者相比,西地那非使用者在这两个阶段的 RER 均较低(P = 0.02,0.01)。此外,西地那非使用者的静息舒张压(DBP)明显降低(p = 0.02)。此外,西地那非使用者与非使用者相比,在改良医学研究委员会(mMRC)评分、慢性阻塞性肺病评估测试(CAT)评分或肺活量参数方面没有明显差异。我们的研究结果表明,接受西地那非治疗的继发性肺动脉高压慢性阻塞性肺疾病患者与未接受西地那非治疗的患者在总体运动能力、症状或肺活量指标方面均无明显差异。
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