Literature DB >> 24713588

Orthodeoxia and postural orthostatic tachycardia in patients with pulmonary arteriovenous malformations: a prospective 8-year series.

V Santhirapala1, B Chamali2, H McKernan3, H C Tighe3, L C Williams3, J T Springett3, H R Bellenberg4, A J Whitaker4, C L Shovlin5.   

Abstract

Postural changes in 258 patients with pulmonary arteriovenous malformations (PAVMs) reviewed between 2005 and 2013 were evaluated prospectively using validated pulse oximetry methods. Of the 257 completing the test, 75 (29%) demonstrated orthodeoxia with an oxygen saturation fall of at least 2% on standing. None described platypnoea (dyspnoea on standing). The heart rate was consistently higher in the erect posture: 74 (29%) had a postural orthostatic tachycardia of ≥20 min(-1), and in 25 (10%) this exceeded 30 min(-1). Orthostatic tachycardia was more pronounced in PAVM patients than controls without orthodeoxia (age-adjusted coefficient 5.5 (95% CIs 2.6, 8.4) min(-1), p<0.001). For PAVM patients, the age-adjusted pulse rise was 0.79 min(-1) greater for every 1% greater drop in oxygen saturation on standing (p<0.001). In contrast to the postural orthostatic tachycardia syndrome, in this population, there was a trend for more pronounced orthostatic tachycardia to be associated with better exercise tolerance. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Hypoxaemia; Oxygen; Rare lung disease

Mesh:

Year:  2014        PMID: 24713588     DOI: 10.1136/thoraxjnl-2014-205289

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


  13 in total

Review 1.  Contemporary Management of Pulmonary Arteriovenous Malformations.

Authors:  Nicholas Rauh; John Gurley; Sibu Saha
Journal:  Int J Angiol       Date:  2017-09-18

Review 2.  Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations: clinical aspects.

Authors:  Nathaniel M Meier; Michael L Foster; John T Battaile
Journal:  Cardiovasc Diagn Ther       Date:  2018-06

Review 3.  Pulmonary arteriovenous malformations.

Authors:  Claire L Shovlin
Journal:  Am J Respir Crit Care Med       Date:  2014-12-01       Impact factor: 21.405

4.  Platypnoea-orthodeoxia syndrome in COVID-19.

Authors:  Adarsh Aayilliath K; Komal Singh; Animesh Ray; Naveet Wig
Journal:  BMJ Case Rep       Date:  2021-05-05

5.  Hypoxaemia, sport and polycythaemia: a case from Imperial College London.

Authors:  Wakana Yasuda; James E Jackson; D Mark Layton; Claire L Shovlin
Journal:  Thorax       Date:  2015-04-08       Impact factor: 9.139

Review 6.  Optimal management of hereditary hemorrhagic telangiectasia.

Authors:  Neetika Garg; Monica Khunger; Arjun Gupta; Nilay Kumar
Journal:  J Blood Med       Date:  2014-10-15

7.  Veterans Specific Activity Questionnaire (VSAQ): a new and efficient method of assessing exercise capacity in patients with pulmonary arteriovenous malformations.

Authors:  Filip Gawecki; Jonathan Myers; Claire L Shovlin
Journal:  BMJ Open Respir Res       Date:  2019-03-01

8.  Circulatory contributors to the phenotype in hereditary hemorrhagic telangiectasia.

Authors:  Claire L Shovlin
Journal:  Front Genet       Date:  2015-04-09       Impact factor: 4.599

9.  Orthodeoxia without Platypnea in Hereditary Hemorrhagic Telangiectasia in the Presence of a Cerebral Abscess and Multiple Pulmonary Arteriovenous Malformations: Unusual Complications and Transcatheter Endovascular Treatment.

Authors:  Carlos Salazar; Jacky Bruce Blank; Veronica Palmero
Journal:  Case Rep Pulmonol       Date:  2017-10-12

10.  Long-term outcomes of patients with pulmonary arteriovenous malformations considered for lung transplantation, compared with similarly hypoxaemic cohorts.

Authors:  Claire L Shovlin; Elisabetta Buscarini; J Michael B Hughes; David J Allison; James E Jackson
Journal:  BMJ Open Respir Res       Date:  2017-10-13
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