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Pulmonary pulse transit time: a novel echocardiographic indicator of hemodynamic and vascular alterations in pulmonary hypertension and pulmonary fibrosis.
Wibmer, Thomas; Rüdiger, Stefan; Scharnbeck, Dominik; Radermacher, Michael; Markovic, Sinisa; Stoiber, Kathrin M; Rottbauer, Wolfgang; Schumann, Christian.
Afiliação
  • Wibmer T; Department of Internal Medicine II, University Hospital of Ulm, Ulm, Germany.
  • Rüdiger S; Department of Internal Medicine II, University Hospital of Ulm, Ulm, Germany.
  • Scharnbeck D; Department of Internal Medicine II, University Hospital of Ulm, Ulm, Germany.
  • Radermacher M; Department of Internal Medicine II, University Hospital of Ulm, Ulm, Germany.
  • Markovic S; Department of Internal Medicine II, University Hospital of Ulm, Ulm, Germany.
  • Stoiber KM; Department of Internal Medicine II, University Hospital of Ulm, Ulm, Germany.
  • Rottbauer W; Department of Internal Medicine II, University Hospital of Ulm, Ulm, Germany.
  • Schumann C; Department of Internal Medicine II, University Hospital of Ulm, Ulm, Germany.
Echocardiography ; 32(6): 904-11, 2015 Jun.
Article em En | MEDLINE | ID: mdl-25264113
ABSTRACT

INTRODUCTION:

Pulse transit time (PTT) is generally assumed to be a surrogate marker for blood pressure changes and arterial stiffness. The aim was to evaluate whether pulmonary PTT (pPTT) may be noninvasively measured by Doppler echocardiography and whether it might be valuable for detecting pulmonary hemodynamic and vascular alterations.

METHODS:

We defined pPTT as the interval between R-wave in the ECG and the corresponding peak late systolic pulmonary vein flow velocity measured by pw-Doppler in the pulmonary vein. Twelve consecutive patients with pulmonary hypertension (PH) and 12 subjects without any cardiovascular or respiratory disease were included in the study. All patients underwent a standard echocardiography including pPTT measurement.

RESULTS:

In the PH group, 5 patients had idiopathic pulmonary arterial hypertension (WHO 1), 1 patient PH associated with connective tissue disease (CTD, WHO 1) without pulmonary fibrosis (PF), and 6 patients PH associated with PF either due to CTD (WHO 1) or other etiology (WHO 3). Mean pPTT was significantly shorter in the PH group (138.0 ± 16.78 msec; P < 0.0001) than in the control group (383.5 ± 23.84 msec). Within the PH group, the subgroup of patients with PF showed significantly shorter mean pPTT (93.50 ± 15.47 msec; P = 0.004) than the subgroup of patients with PH without PF (182.6 ± 14.35 msec).

CONCLUSIONS:

The results of this study suggest that pPTT might be an interesting surrogate marker of pulmonary hemodynamic and vascular alterations in PH and PF. Further studies are warranted to evaluate the possible influence of other variables on pPTT.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrose Pulmonar / Ecocardiografia / Análise de Onda de Pulso / Hipertensão Pulmonar Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Echocardiography Assunto da revista: CARDIOLOGIA / DIAGNOSTICO POR IMAGEM Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrose Pulmonar / Ecocardiografia / Análise de Onda de Pulso / Hipertensão Pulmonar Tipo de estudo: Diagnostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Revista: Echocardiography Assunto da revista: CARDIOLOGIA / DIAGNOSTICO POR IMAGEM Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Alemanha