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Cardiac output measurements during high-risk Cesarean section using electrical bioreactance or arterial waveform analysis: assessment of agreement.
Gutierrez, J; Perry, H; Columb, M; Bampoe, S; Thilaganathan, B; Khalil, A.
Afiliação
  • Gutierrez J; Fetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, University of London, London, UK.
  • Perry H; Fetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, University of London, London, UK.
  • Columb M; Vascular Biology Research Centre, Molecular and Clinical Sciences Research Institute, St George's University of London, London, UK.
  • Bampoe S; Manchester University Hospitals NHS Foundation Trust, Wythenshawe Hospital, Manchester, UK.
  • Thilaganathan B; Centre for Anaesthesia and Perioperative Medicine, University College London, London, UK.
  • Khalil A; Fetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, University of London, London, UK.
Ultrasound Obstet Gynecol ; 54(2): 232-238, 2019 Aug.
Article em En | MEDLINE | ID: mdl-30302868
ABSTRACT

OBJECTIVE:

Maternal hemodynamics change significantly during Cesarean section complicated by massive hemorrhage or severe hypertensive disease. Cardiac output (CO) monitoring aids early, goal-directed hemodynamic therapy. The aim of this study was to record hemodynamic changes observed during Cesarean section in pregnancies at high risk of hemodynamic instability, using invasive (LiDCOrapid™) and non-invasive (NICOM®) devices, and to assess agreement between the two devices in measuring CO.

METHODS:

Simultaneous intraoperative hemodynamic measurements were taken using the LiDCOrapid and NICOM devices, following standardized techniques, in women at high risk of hemodynamic instability undergoing Cesarean section. Agreement in CO measurements between the two devices was assessed using Bland-Altman plots and the agreementtolerability index (ATI). Agreement analyses were performed for repeated measures in subjects, using centiles.

RESULTS:

From 10 women, 307 paired measurements were analyzed. Mean bias (defined as the mean difference in CO measurements between the LiDCOrapid and NICOM devices) was 3.05 (95% CI, 1.89 to 4.21) L/min. Limits of agreement ranged from -1.58 (95% CI, -4.47 to -0.14) to 7.68 (95% CI, 6.24 to 10.56) L/min. The resulting agreement interval was 9.26 L/min which returned an ATI of 2.3.

CONCLUSIONS:

There are large mean differences between CO measurements obtained during Cesarean section using the LiDCOrapid and NICOM hemodynamic monitors in pregnant women at high risk of hemodynamic instability, indicating that they should not be considered interchangeable clinically. There is an unacceptably low level of agreement (ATI > 2) in CO measurements between the devices, conferring a high risk of clinical misclassification during massive hemorrhage. Copyright © 2018 ISUOG. Published by John Wiley & Sons Ltd.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Débito Cardíaco / Cesárea / Gravidez de Alto Risco Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Débito Cardíaco / Cesárea / Gravidez de Alto Risco Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2019 Tipo de documento: Article