Abstrakti
Background: Clinical practice guidelines recommend use of buffered crystalloid solutions in critically ill patients but do not distinguish between solutions based on different buffering anions, that is, acetate- versus lactate-buffered solutions. We therefore surveyed relevant physicians about their preferences and attitudes toward each solution. Methods: We conducted an international online survey of anesthesiologists (within perioperative care) and intensive care unit (ICU) physicians. The survey comprised 13 questions on respondents' attitudes and preferences regarding the use of acetate- and/or lactate-buffered crystalloid solutions, including their opinions on a potential clinical trial comparing these solutions and the clinical importance of such a trial. Results: A total of 1321 respondents participated, with a response rate of 34%, ranging from 14% to 96% across 18 countries. Most surveyed physicians reported using buffered crystalloid solutions “very often” (76%) or “often” (16%). Availability of acetate- and lactate-buffered solutions varied, as 35% of respondents reported having both types available, 35% reported having only acetate-, and 24% reported having only lactate-buffered solutions available. Most respondents (87%) would support a randomized trial in adult emergency surgical patients and ICU patients comparing an acetate- versus lactate-buffered crystalloid solution. The median rating of the clinical importance of this question was 5 (interquartile range 4–6) on a scale from 1 to 9. Conclusions: In this international survey, the reported use of buffered crystalloid solutions was high. Availability of the different solutions varied widely. The support for a potential randomized trial was high, with the clinical importance rated important but not critical by most respondents.
| Alkuperäiskieli | Englanti |
|---|---|
| Artikkeli | e14553 |
| Julkaisu | Acta Anaesthesiologica Scandinavica |
| Vuosikerta | 69 |
| Numero | 1 |
| Varhainen verkossa julkaisun päivämäärä | 3 jouluk. 2024 |
| DOI - pysyväislinkit | |
| Tila | Julkaistu - tammik. 2025 |
| OKM-julkaisutyyppi | A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä |
Rahoitus
P. S., K. L. E., A. P., and M. H. M. are affiliated with the Department of Intensive Care at Rigshospitalet, which has received funding for other projects from the Novo Nordisk Foundation. A. P. has received an honorarium from Novartis for participation in an advisory board. J. D. W. has consulted for Menarini, MSD, Pfizer, ThermoFisher, and Viatris with fees and honoraria paid to institution. J. H. has received an honorarium from Paion for participation in an advisory board. A. R. B. received speaker or consultancy fees from Nutricia Danone and VIPUN Medical and she is holding a grant from the Estonian Research Council (PRG1255). A. K. consults for Medtronic, Edwards Life Sciences, Philips Research North America, Baxter, GE Healthcare, Potrero Medical, Retia Medical, and Caretaker Medical. P. Y. reports that this research was completed during the tenure of a Clinical Practitioner Fellowship awarded by the Health Research Council of New Zealand. The remaining authors declare no conflict of interests. No external organizations had influence on the design, conduct, or the decision to publish the results of this article.
| Rahoittajat | Rahoittajan numero |
|---|---|
| VIPUN Medical | |
| Health Research Council of New Zealand | |
| Eesti Teadusagentuur | PRG1255 |
Julkaisufoorumi-taso
- Jufo-taso 1
!!ASJC Scopus subject areas
- Anesthesiology and Pain Medicine
Sormenjälki
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