Cost effectiveness and clinical efficacy of patent foramen ovale closure as compared to medical therapy in cryptogenic stroke patients: A detailed cost analysis and meta-analysis of randomized controlled trials

被引:5
作者
Pickett, Christopher A. [1 ,2 ]
Villines, Todd C. [1 ,3 ]
Resar, Jon R. [4 ,5 ]
Hulten, Edward A. [1 ,6 ]
机构
[1] Uniformed Serv Univ Hlth Sci, Bethesda, MD 20814 USA
[2] Brooke Army Med Ctr, San Antonio, TX USA
[3] Walter Reed Natl Mil Med Ctr, Bethesda, MD USA
[4] Johns Hopkins Univ Hosp, Baltimore, MD 21287 USA
[5] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[6] Evans Army Hosp, Serv Cardiol, Ft Carson, CO USA
关键词
cryptogenic stroke; Stroke; Patent foramen ovale; Cost analysis; Meta-analysis; PERCUTANEOUS CLOSURE; ISCHEMIC-STROKE; RISK; RECOMMENDATIONS; CLOPIDOGREL; ASPIRIN; QUALITY; UPDATE; HEALTH;
D O I
10.1016/j.ijcard.2018.07.099
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Up to half the patients with cryptogenic stroke under the age of 55 years have been found to have a PM. Observational studies have demonstrated a benefit from closure of PFO and several RCTs have shown a trend toward benefit. The cost and clinical effectiveness of PFO closure is unclear. Methods and results: We searched for RCTs of PFO closure in patients with cryptogenic stroke and performed a detailed cost analysis and meta-analysis of treatment outcomes based on the results of the meta-analysis. Five RCTs containing 3404 patients with cryptogenic stroke were included. Of these 1829 underwent PFO closure and 1611 received medical therapy. Mean follow-up was 4.0 years. PFO closure achieved cost effectiveness (<$50,000/Quality-adjusted life-year gained) 2.7 years (95% Confidence Interval (CI) 22-3.4) after closure. The incremental cost to prevent one combined end point (CEP, combined transient ischemic attack (TIA), stroke, and death) by PFO closure was $535,655(95% CI $458,329-$642,674). After 55.4 years (95%CI 51.1-60.5) of follow-up, the per patient total cost of medical therapy exceeded that of PFO closure. PFO closure demonstrated clinical efficacy with a decreased risk of CEP (pooled hazard ratio (HR = 0.43(95%CI 0.27-0.59))) and a decreased risk of stroke (HR = 0.29(95%CI 0.02-0.57)). Conclusions: In comparison to medical therapy alone, PFO closure appears to be cost-effective and clinically efficacious. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:74 / 79
页数:6
相关论文
共 41 条
[1]   Cost-Effectiveness of Targeting Patients Undergoing Percutaneous Coronary Intervention for Therapy With Bivalirudin Versus Heparin Monotherapy According to Predicted Risk of Bleeding [J].
Amin, Amit P. ;
Marso, Steven P. ;
Rao, Sunil V. ;
Messenger, John ;
Chan, Paul S. ;
House, John ;
Kennedy, Kevin ;
Robertus, Katherine ;
Cohen, David J. ;
Mahoney, Elizabeth M. .
CIRCULATION-CARDIOVASCULAR QUALITY AND OUTCOMES, 2010, 3 (04) :358-U47
[2]  
[Anonymous], RL34208 C RES SERV
[3]  
[Anonymous], PER LIF TABL
[4]  
[Anonymous], PFO OCCL INSTR US
[5]  
[Anonymous], COCHRANE HDB SYSTEMA
[6]  
[Anonymous], PHYS FEE SCHED 2017
[7]   The 'NICE' approach to technology assessment: An economics perspective [J].
Birch S. ;
Gafni A. .
Health Care Management Science, 2004, 7 (1) :35-41
[8]   Association of Aspirin Use With Major Bleeding in Patients With and Without Diabetes [J].
De Berardis, Giorgia ;
Lucisano, Giuseppe ;
D'Ettorre, Antonio ;
Pellegrini, Fabio ;
Lepore, Vito ;
Tognoni, Gianni ;
Nicolucci, Antonio .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2012, 307 (21) :2286-2294
[9]   Aspirin and clopidogrel compared with clopidogrel alone after recent ischaemic stroke or transient ischaemic attack in high-risk patients (MATCH): randomised, double-blind, placebo-controlled trial [J].
Diener, HC ;
Bogousslavsky, J ;
Brass, LM ;
Cimminiello, C ;
Csiba, L ;
Kaste, M ;
Leys, D ;
Matias-Guiv, J ;
Rupprecht, HJ .
LANCET, 2004, 364 (9431) :331-337
[10]   European stroke prevention study .2. Dipyridamole and acetylsalicylic acid in the secondary prevention of stroke [J].
Diener, HC ;
Cunha, L ;
Forbes, C ;
Sivenius, J ;
Smets, P ;
Lowenthal, A .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1996, 143 (1-2) :1-13