Embolisation for pulmonary arteriovenous malformation

被引:27
作者
Hsu, Charlie C-T [1 ]
Kwan, Gigi N. C. [2 ]
Evans-Barns, Hannah [3 ]
van Driel, Mieke L. [4 ,5 ,6 ]
机构
[1] Univ Toronto, Dept Med Imaging, 4th Floor,263 McCaul St, Toronto, ON M5T 1W7, Canada
[2] Princess Alexandra Hosp, Dept Med Imaging, Brisbane, Qld, Australia
[3] Univ Melbourne, Fac Med Dent & Hlth Sci, Melbourne, Vic, Australia
[4] Univ Queensland, Fac Med, Primary Care Clin Unit, Brisbane, Qld, Australia
[5] Bond Univ, Ctr Res Evidence Based Practice CREBP, Gold Coast, Australia
[6] Univ Ghent, Dept Family Med & Primary Hlth Care, Ghent, Belgium
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2018年 / 01期
关键词
Arteriovenous Malformations [therapy; Embolization; Therapeutic [adverse effects; methods; Pulmonary Artery [abnormalities; Pulmonary Veins [abnormalities; Humans; HEREDITARY HEMORRHAGIC TELANGIECTASIA; FOLLOW-UP; EMBOLOTHERAPY; CT; ANGIOARCHITECTURE; PREVALENCE; MORTALITY; CHILDREN; EFFICACY; OUTCOMES;
D O I
10.1002/14651858.CD008017.pub5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Pulmonary arteriovenous malformations are abnormal direct connections between the pulmonary artery and pulmonary vein which result in a right-to-left shunt. They are associated with substantialmorbidity and mortality mainly from the effects of paradoxical emboli. Potential complications include stroke, cerebral abscess, pulmonary haemorrhage and hypoxaemia. Embolisation is an endovascular intervention based on the occlusion of the feeding arteries the pulmonary arteriovenous malformations thus eliminating the abnormal right-to-left-shunting. This is an update of a previously published review. Objectives To determine the efficacy and safety of embolisation in patients with pulmonary arteriovenous malformations including a comparison with surgical resection and different embolisation devices. Search methods We searched the Cystic Fibrosis and Genetic Disorders Group's Trials Register; date of last search: 10 April 2017. We also searched the following databases: the Australian New Zealand Clinical Trials Registry; Clinical Trials.gov; International Standard Randomised Controlled Trial Number Register; International Clinical Trials Registry Platform Search Portal (last searched 27 August 2017). to be updated We checked cross-references and searched references from review articles. Selection criteria Trials in which individuals with pulmonary arteriovenous malformations were randomly allocated to embolisation compared to no treatment, surgical resection or embolisation using a different embolisation device. Data collection and analysis Studies identified for potential inclusion were independently assessed for eligibility by two authors, with excluded studies further checked by a third author. No trials were identified for inclusion in the review and hence no analysis was performed. Main results There were no randomised controlled trials included in the review; one ongoing trial has been identified which may be eligible for inclusion in the future. Authors' conclusions There is no evidence from randomised controlled trials for embolisation of pulmonary arteriovenous malformations. However, randomised controlled trials are not always feasible on ethical grounds. Accumulated data from observational studies suggest that embolisation is a safe procedure which reduces morbidity and mortality. A standardised approach to reporting with long-term follow-up through registry studies can help to strengthen the evidence for embolisation in the absence of randomised controlled trials.
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页数:21
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共 53 条
[1]  
Abdalla SA, 2006, J MED GENET, V43, P97
[2]   Hereditary hemorrhagic telangiectasia: An overview of diagnosis and management in the molecular era for clinicians [J].
Bayrak-Toydemir, P ;
Mao, R ;
Lewin, S ;
McDonald, J .
GENETICS IN MEDICINE, 2004, 6 (04) :175-191
[3]  
Borrero CG, 2006, J RADIOLOGY NURSING, V25, P33
[4]   Pulmonary arteriovenous malformation treated with embolotherapy: Systemic collateral supply at multidetector CT angiography after 2-20-year follow-up [J].
Brillet, Pierre-Yves ;
Dumont, Philippe ;
Bouaziz, Nebil ;
Duhamel, Alain ;
Laurent, Francois ;
Remy, Jacques ;
Remy-Jardin, Martine .
RADIOLOGY, 2007, 242 (01) :267-276
[5]  
Cil B, 2008, DIAGN INTERV RADIOL, V14, P35
[6]   Pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia [J].
Cottin, V ;
Plauchu, H ;
Bayle, JY ;
Barthelet, M ;
Revel, D ;
Cordier, JF .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 169 (09) :994-1000
[7]   Long-term follow-up in 12 children with pulmonary arteriovenous malformations: confirmation of hereditary hemorrhagic telangiectasia in all cases [J].
Curie, Aurcre ;
Lesca, Gaetan ;
Cottin, Vincent ;
Edery, Patrick ;
Bellon, Gabriel ;
Faughnan, Marie E. ;
Plauchu, Henri .
JOURNAL OF PEDIATRICS, 2007, 151 (03) :299-306
[8]   Genetic epidemiology of hereditary hemorrhagic telangiectasia in a local community in the northern part of Japan [J].
Dakeishi, M ;
Shioya, T ;
Wada, Y ;
Shindo, T ;
Otaka, K ;
Manabe, M ;
Nozaki, J ;
Inoue, S ;
Koizumi, A .
HUMAN MUTATION, 2002, 19 (02) :140-148
[9]   PULMONARY ARTERIOVENOUS-MALFORMATIONS - RESULTS OF TREATMENT WITH COIL EMBOLIZATION IN 53 PATIENTS [J].
DUTTON, JAE ;
JACKSON, JE ;
HUGHES, JMB ;
WHYTE, MKB ;
PETERS, AM ;
USSOV, W ;
ALLISON, DJ .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1995, 165 (05) :1119-1125
[10]   Diffuse pulmonary arteriovenous malformations - Characteristics and prognosis [J].
Faughnan, ME ;
Lui, YW ;
Wirth, JA ;
Pugash, RA ;
Redelmeier, DA ;
Hyland, RH ;
White, RI .
CHEST, 2000, 117 (01) :31-38