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Haematocrit monitoring and blood volume estimation during continuous renal replacement therapy.
Baldwin, Ian; Maeda, Akinori; Bellomo, Rinaldo; See, Emily.
Afiliação
  • Baldwin I; Department of Intensive Care, Austin Hospital, Melbourne, Australia. Electronic address: ian.baldwin@austin.org.au.
  • Maeda A; Department of Intensive Care, Austin Hospital, Melbourne, Australia; Department of Emergency and Critical Care Medicine, The University of Tokyo Hospital, Tokyo, Japan.
  • Bellomo R; Department of Intensive Care, Austin Hospital, Melbourne, Australia; Department of Emergency and Critical Care Medicine, The University of Tokyo Hospital, Tokyo, Japan; ANZICS-Research Centre, Monash University School and Public Health and Preventive Medicine, Monash University, Melbourne, Australia
  • See E; Department of Intensive Care, Austin Hospital, Melbourne, Australia; Department of Intensive Care, Royal Melbourne Hospital, Melbourne, Australia.
Aust Crit Care ; 37(4): 632-637, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38245397
ABSTRACT

BACKGROUND:

Continuous haemoglobin, venous blood oxygen saturation, and haematocrit (Hct) monitoring is currently not applied during continuous renal replacement therapy (CRRT). Such Hct monitoring enables estimation of changes in blood volume as percentage change (ΔBV%) from therapy start time and is incorporated into intermittent haemodialysis machines but not CRRT machines despite its potential to optimise fluid management in CRRT patients.

METHODS:

To overcome this problem, we used a standalone monitor (CRIT-LINE®IV, Fresenius Medical Care, Concord, USA) with an associated in-line blood chamber (CRIT-LINE®IV Blood Chamber, Fresenius Medical Care, Concord, USA) and designed our own adaptor connection piece (TekMed and Morriset, Melbourne and Brisbane, Australia) to allow these readings at the vascular access outflow and recorded data for estimated Hct and derived ΔBV% during CRRT.

RESULTS:

We report on this technique with an illustrative case example and 12 h of CRRT data on the fluid loss rate prescribed, hourly net patient fluid loss (range 0-308 mL/h), mean arterial pressure, norepinephrine dose (range 5-14 mcg/min), estimated continuous Hct and ΔBV%, and the otherwise undetected diagnosis of an approximate 15 % decrease in blood volume during the CRRT.

CONCLUSION:

We have described a technical CRRT circuit modification that can facilitate a previously unavailable assessment of fluid shifts during CRRT. Further application in clinical trials is now possible.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Volume Sanguíneo / Terapia de Substituição Renal Contínua Limite: Humans / Male Idioma: En Revista: Aust Crit Care Assunto da revista: ENFERMAGEM / TERAPIA INTENSIVA Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Volume Sanguíneo / Terapia de Substituição Renal Contínua Limite: Humans / Male Idioma: En Revista: Aust Crit Care Assunto da revista: ENFERMAGEM / TERAPIA INTENSIVA Ano de publicação: 2024 Tipo de documento: Article