scispace - formally typeset
Journal ArticleDOI

Dépistage de l’hypertension artérielle pulmonaire au cours de la sclérodermie systémique : comparaison de l’algorithme DETECT à une discussion pluridisciplinaire en centre de compétence

Reads0
Chats0
TLDR
L’application de l’algorithme DETECT a permis de depister toutes les HTAP diagnostiquees suite a the reunion of the concertation pluridisciplinaire.
Abstract
Resume Introduction L’hypertension arterielle pulmonaire (HTAP) est une complication grave de la sclerodermie systemique (SSc), importante a depister L’etude DETECT a propose en 2013 un algorithme de depistage Nous avons compare les indications au catheterisme cardiaque droit posees par cet algorithme, a celles retenues par une reunion de concertation pluridisciplinaire en centre de competences Patients et methodes Etude prospective monocentrique non interventionnelle ayant inclus les patients suivis pour SSc, pour qui les donnees etaient suffisantes pour appliquer l’algorithme DETECT Nous avons calcule l’algorithme et compare ses indications a la realisation d’un catheterisme cardiaque droit avec celles retenues dans notre centre suite a une reunion de concertation pluridisciplinaire Resultats Au total, 117 patients ont ete inclus En appliquant l’algorithme a l’ensemble de la population, l’indication du catheterisme etait retenue pour 70 d’entre eux ; la reunion de concertation pluridisciplinaire avait egalement retenu cette indication pour 15 d’entre eux dont 7 avaient finalement une HTAP En appliquant l’algorithme aux patients ayant une DLCO  Conclusion L’application de l’algorithme DETECT a permis de depister toutes les HTAP diagnostiquees suite a la reunion de concertation pluridisciplinaire Cependant, il multiplie par trois le nombre de catheterisme cardiaque droit a realiser

read more

Citations
More filters
Journal ArticleDOI

The prevalence and incidence rate of pulmonary arterial hypertension in systemic sclerosis: Systematic review and meta-analysis

TL;DR: The present study aimed to assess the prevalence and incidence rate of pulmonary arterial hypertension (PAH) in Systemic Sclerosis (SSc) in MEDLINE and SCOPUS from June 1962 to May 2019 and the terms: ("Scleroderma, Systemic"[MesH]) AND "Hypertension, Pulmonary"[MESH].
Journal ArticleDOI

Screening for the early detection of pulmonary arterial hypertension in patients with systemic sclerosis: A systematic review and meta-analysis of long-term outcomes

TL;DR: In this article, a systematic review of the evidence for screening for pulmonary arterial hypertension (PAH) in patients with systemic sclerosis (scleroderma, SSc) is presented.
Journal ArticleDOI

Screening for pulmonary arterial hypertension in systemic sclerosis: Now or never!

TL;DR: The current clinical and research implications of the screening for the early detection of SSc-PAH are addressed and best practice recommendations are for asymptomatic patients with SSc and S Sc-spectrum disorder to be screened annually.
References
More filters
Journal ArticleDOI

2013 classification criteria for systemic sclerosis: An american college of rheumatology/European league against rheumatism collaborative initiative

Frank H J van den Hoogen, +46 more
TL;DR: The ACR/EULAR classification criteria for SSc performed better than the 1980 ACR criteria and should allow for more patients to be classified correctly as having the disease.
Journal ArticleDOI

Special article2015 ESC/ERS Guidelines for the Diagnosis and Treatment of Pulmonary Hypertension

TL;DR: This article is being published concurrently in the European Heart Journal and the European Respiratory Journal and is identical except for minor stylistic and spelling differences in keeping with each journal’s style.
Journal ArticleDOI

Changes in causes of death in systemic sclerosis, 1972-2002.

TL;DR: The change in the pattern of scleroderma-related deaths over the past 30 years demonstrates that the lung (both pulmonary hypertension and PF) is the primary cause of sclerosis- related deaths today.
Related Papers (3)