Literature DB >> 20379644

Etiological frequency of pulmonary hypertension in a reference outpatient clinic in Bahia, Brazil.

Cesar Machado1, Isis Brito, Denile Souza, Luis Cláudio Correia.   

Abstract

BACKGROUND: Pulmonary hypertension (PH) results from several etiologies, with possible geographic influences; however, few studies have described the etiological frequency of PH, especially in our country. It is not clear whether there is an association between etiology and pulmonary pressure level or symptom intensity.
OBJECTIVES: 1) to describe the etiological prevalence of PH in the state of Bahia, Brazil; 2) to evaluate whether the etiology is a determinant factor for the pulmonary pressure level; 3) to evaluate whether the etiology is a determinant factor for functional class; 4) to identify the other predictors of pulmonary pressure level and functional class.
METHODS: The present was an observational, cross-sectional study that analyzed individuals with PH treated at the Magalhaes Neto Outpatient Clinic, between June 2005 and December 2007. PH was defined as pulmonary artery systolic pressure (PASP) > 40 mmHg measure at the echocardiogram. Patients with chronic obstructive pulmonary disease or ventricular disease were excluded from the study.
RESULTS: A total of 48 patients with PASP = 86 +/- 24 mmHg were studied. Regarding the etiology, 42% of the patients were classified as idiopathic, followed by 25% as schistosomatic, 19% as congenital cardiopathy and 10% of chronic pulmonary embolism. A longer time of disease predicted higher pressures in patients with cardiopathy. Individuals with schistosomiasis had the best functional performance when compared to the others (456 +/- 58 vs. 299 +/- 138 meters, p=0.005). The schistosomatic etiology and younger age presented better functional class.
CONCLUSIONS: 1) the idiopathic classification is the most prevalent, with schistosomiasis being the most frequent specific cause in our country; 2) patients with schistosomatic etiology and of younger age present better functional class. 3) the congenital cardiopathy results in a higher pressure level in the pulmonary artery, probably due to the longer duration of the disease.

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Year:  2009        PMID: 20379644     DOI: 10.1590/s0066-782x2009001200019

Source DB:  PubMed          Journal:  Arq Bras Cardiol        ISSN: 0066-782X            Impact factor:   2.000


  4 in total

1.  Prevalence and profile of congenital heart disease and pulmonary hypertension in Down syndrome in a pediatric cardiology service.

Authors:  Felipe Alves Mourato; Lúcia Roberta R Villachan; Sandra da Silva Mattos
Journal:  Rev Paul Pediatr       Date:  2014-06

Review 2.  Schistosomiasis-associated pulmonary hypertension.

Authors:  Demosthenes G Papamatheakis; Ana Olga H Mocumbi; Nick H Kim; Jess Mandel
Journal:  Pulm Circ       Date:  2014-12       Impact factor: 3.017

3.  Pulmonary artery pressure, gender, menopause, and pregnancy in schistosomiasis-associated pulmonary hypertension.

Authors:  Anderson C Armstrong; Ângela M P Bandeira; Luis C L Correia; Humberto C O Melo; Carlos A M Silveira; Eugênio Albuquerque; Jeová C Moraes; Antônio M L Silva; João A C Lima; Dário C Sobral Filho
Journal:  Arq Bras Cardiol       Date:  2013-07-02       Impact factor: 2.000

Review 4.  Schistosomiasis Pulmonary Arterial Hypertension.

Authors:  Jean Pierre Sibomana; Aloma Campeche; Roberto J Carvalho-Filho; Ricardo Amorim Correa; Helena Duani; Virginia Pacheco Guimaraes; Joan F Hilton; Biruk Kassa; Rahul Kumar; Michael H Lee; Camila M C Loureiro; Sula Mazimba; Claudia Mickael; Rudolf K F Oliveira; Jaquelina S Ota-Arakaki; Camila Farnese Rezende; Luciana C S Silva; Edford Sinkala; Hanan Yusuf Ahmed; Brian B Graham
Journal:  Front Immunol       Date:  2020-12-10       Impact factor: 7.561

  4 in total

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