Ryan John J, Butrous Ghazwan, Maron Bradley A
Division of Cardiology, University Hospital, University of Utah, Salt Lake City, Utah, USA.
School of Pharmacy, University of Kent, Kent, United Kingdom.
Pulm Circ. 2014 Sep;4(3):441-51. doi: 10.1086/677357.
The extent to which pulmonary arterial hypertension (PAH) experts share common practice patterns that are in alignment with published expert consensus recommendations is unknown. Our objective was to characterize the clinical management strategies used by an international cohort of self-identified PAH experts. A 32-item questionnaire composed mainly of rank order or Likert scale questions was distributed via the Internet (August 5, 2013, through January 20, 2014) to four international pulmonary vascular disease organizations. The survey respondents (N = 105) were field experts reporting 11.6 ± 8.7 years of PAH experience. Likert scale responses (1 = disagree, 7 = agree) were 3.0-5.0, indicating a disparity in opinions, for 78% of questions. Respondent (dis)agreement scores were 4.4 ± 2.2 for use of expert recommendations to determine catheterization timing in PAH. For PAH patients without cardiogenic shock or known vasoreactivity status, the most and least preferred first-line therapies (1 = most preferred, 5 = least preferred) were phosphodiesterase type 5 inhibitors (PDE-Vi) and subcutaneous prostacyclin analogues, respectively (1.4 ± 0.8 vs. 4.0 ± 1.1; P < 0.05). Compared with US-practicing clinicians (N = 46), non-US-practicing clinicians (N = 57) favored collaboration between cardiology and pulmonary medicine for clinical decision making (1 = disagree, 7 = agree; 3.1 ± 2.2 vs. 4.8 ± 2.2; P < 0.0001) and PDE-Vi (6.5% vs. 22.4%) as first-line therapy for PAH patients with cardiogenic shock but were less likely to perform vasoreactivity testing in patients with lung disease-induced pulmonary hypertension (4.3 ± 2.1 vs. 2.2 ± 1.6; P < 0.0001). In conclusion, practice patterns among PAH experts diverge from consensus recommendations and differ by practice location, suggesting that opportunity may exist to improve care quality for this highly morbid cardiopulmonary disease.
肺动脉高压(PAH)专家在多大程度上共享与已发表的专家共识建议一致的常见实践模式尚不清楚。我们的目标是描述一组国际上自我认定的PAH专家所采用的临床管理策略。一份主要由排序或李克特量表问题组成的32项问卷于2013年8月5日至2014年1月20日通过互联网分发给四个国际肺血管疾病组织。调查对象(N = 105)为现场专家,报告有11.6±8.7年的PAH经验。对于78%的问题,李克特量表的回答(1 = 不同意,7 = 同意)为3.0 - 5.0,表明意见存在差异。在使用专家建议来确定PAH患者的导管插入术时机方面,调查对象的(不)同意得分是4.4±2.2。对于没有心源性休克或已知血管反应性状态的PAH患者,最受欢迎和最不受欢迎的一线治疗方法(1 = 最受欢迎,5 = 最不受欢迎)分别是5型磷酸二酯酶抑制剂(PDE - Vi)和皮下前列环素类似物(1.4±0.8对4.0±1.1;P < 0.05)。与美国执业临床医生(N = 46)相比,非美国执业临床医生(N = 57)更倾向于心脏病学和肺病学之间合作进行临床决策(1 = 不同意,7 = 同意;3.1±2.2对4.8±2.2;P < 0.0001),并且更倾向于将PDE - Vi作为有心源性休克的PAH患者的一线治疗方法(6.5%对22.4%),但在患有肺部疾病引起的肺动脉高压的患者中进行血管反应性测试的可能性较小(4.3±2.1对2.2±1.6;P < 0.0001)。总之,PAH专家之间的实践模式与共识建议不同,并且因执业地点而异,这表明可能有机会改善这种高发病率心肺疾病的护理质量。