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The validity of central venous to arterial carbon dioxide difference to predict adequate fluid management during living donor liver transplantation. A prospective observational study

BACKGROUND: To assess the validity of central and pulmonary veno-arterial CO(2) gradients to predict fluid responsiveness and to guide fluid management during liver transplantation. METHODS: In adult recipients (ASA III to IV) scheduled for liver transplantation, intraoperative fluid management was...

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Detalles Bibliográficos
Autores principales: ELAyashy, Mohamed, Hosny, Hisham, Hussein, Amr, AbdelAal Ahmed Mahmoud, Ahmed, Mukhtar, Ahmed, El-Khateeb, Amira, Wagih, Mohamed, AboulFetouh, Fawzia, Abdelaal, Amr, Said, Hany, Abdo, Mostafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589166/
https://www.ncbi.nlm.nih.gov/pubmed/31228943
http://dx.doi.org/10.1186/s12871-019-0776-9
Descripción
Sumario:BACKGROUND: To assess the validity of central and pulmonary veno-arterial CO(2) gradients to predict fluid responsiveness and to guide fluid management during liver transplantation. METHODS: In adult recipients (ASA III to IV) scheduled for liver transplantation, intraoperative fluid management was guided by pulse pressure variations (PPV). PPV of ≥15% (Fluid Responding Status-FRS) indicated fluid resuscitation with 250 ml albumin 5% boluses repeated as required to restore PPV to < 15% (Fluid non-Responding Status-FnRS). Simultaneous blood samples from central venous and pulmonary artery catheters (PAC) were sent to calculate central venous to arterial CO(2) gap [C(v-a) CO2 gap] and pulmonary venous to arterial CO(2) gap [Pulm(p-a) CO2 gap]. CO and lactate were also measured. RESULTS: Sixty seven data points were recorded (20 FRS and 47 FnRS). The discriminative ability of central and pulmonary CO(2) gaps between the two states (FRS and FnRS) was poor with AUC of ROC of 0.698 and 0.570 respectively. Central CO(2) gap was significantly higher in FRS than FnRS (P = 0.016), with no difference in the pulmonary CO(2) gap between both states. The central and Pulmonary CO(2) gaps are weakly correlated to PPV [r = 0.291, (P = 0.017) and r = 0.367, (P = 0.002) respectively]. There was no correlation between both CO(2) gaps and both CO and lactate. CONCLUSION: Central and the Pulmonary CO(2) gaps cannot be used as valid tools to predict fluid responsiveness or to guide fluid management during liver transplantation. CO(2) gaps also do not correlate well with the changes in PPV or CO. TRIAL REGISTRATION: Clinicaltrials.gov Identifier: NCT03123172. Registered on 31-march-2017.