Author:
Davies-van Es S A,Pennel T C,Brink J,Symons G J,Calligaro G L
Abstract
Background. Pulmonary endarterectomy (PEA) is the only definitive and potentially curative therapy for chronic thromboembolicpulmonary hypertension (CTEPH), associated with impressive improvements in symptoms and haemodynamics. However, it is onlyoffered at a few centres in South Africa. The characteristics and outcomes of patients undergoing PEA in Cape Town have not beenreported previously.Objectives. To assess the difference in World Health Organization functional class (WHO-FC) before and at least 6 weeks after surgery.Methods. We interrogated the adult cardiothoracic surgery database at the University of Cape Town between December 2005 and April 2021 for patients undergoing PEA at Groote Schuur Hospital and a private hospital.Results. A total of 32 patients underwent PEA, of whom 8 were excluded from the final analysis owing to incomplete data or a histological diagnosis other than CTEPH. The work-up of these patients for surgery was variable: all had a computed tomography pulmonary angiogram, 7 (29%) had a ventilation/perfusion scan, 5 (21%) underwent right heart catheterisation, and none had a pulmonary angiogram. The perioperative mortality was 4/24 (17%): 1 patient (4%) had a cardiac arrest on induction of anaesthesia, 2 patients (8%) died of postoperative pulmonary haemorrhage, and 1 patient (4%) died of septic complications in the intensive care unit. Among the survivors, the median (interquartile range) improvement in WHO-FC was 2 (1 - 3) classes (p=0.0004); 10/16 patients (63%) returned to a normal baseline (WHO-FC I).Conclusion. Even in a low-volume centre, PEA is associated with significant improvements in WHO-FC and a return to a normal baseline in survivors.
Publisher
South African Medical Association NPC
Subject
Infectious Diseases,Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine
Reference28 articles.
1. Galiè N, Humbert M, Vachiery JL, et al. 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: The Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT). Eur Heart J 2016;37(1):67-119. https://doi. org/10.1093/eurheartj/ehv317
2. Wilkens H, Konstantinides S, Lang IM, et al. Chronic thromboembolic pulmonary hypertension (CTEPH): Updated recommendations from the Cologne Consensus Conference 2018. Int J Cardiol 2018;272S:69-78. https://doi.org/10.1016/j. ijcard.2018.08.079
3. Pepke-Zaba J, Delcroix M, Lang I, et al. Chronic thromboembolic pulmonary hypertension (CTEPH): Results from an international prospective registry. Circulation 2011;124(18):1973-1981. https://doi.org/10.1161/circulationaha.110.015008
4. De Perrot M, Gopalan D, Jenkins D, et al. Evaluation and management of patients with chronic thromboembolic pulmonary hypertension – consensus statement from the ISHLT. J Heart Lung Transplant 2021;40(11):1301-1326. https://doi.org/10.1016/j. healun.2021.07.020
5. Delcroix M, Kerr K, Fedullo P. Chronic thromboembolic pulmonary hypertension: Epidemiology and risk factors. Ann Am Thorac Soc 2016;13(Suppl 3):S201-S206. https://doi.org/10.1513/AnnalsATS.201509-621AS
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献