Pain and sedation management and monitoring in pediatric intensive care units across Europe: an ESPNIC survey

Author:

Daverio Marco,von Borell Florian,Ramelet Anne-Sylvie,Sperotto Francesca,Pokorna Paula,Brenner Sebastian,Mondardini Maria Cristina,Tibboel Dick,Amigoni Angela,Ista Erwin,Kola Ermira,Vittinghoff Maria,Duval Elim,Polić Branka,Valla Frédéric,Neunhoeffer Felix,Konstantinos Tziouvas,Györgyi Zoltán,Tan Mong Hoi,Hasani Antigona,Poluzioroviene Edita,Balmaks Reinis,Afanetti Mickael,Bentsen Gunnar,Bartkowska-Sniatkowska Alicja,Camilo Cristina,Simic Dusica,López-Fernández Yolanda M.,Mattsson Janet,Özen Hasan,Dmytriiev Dmytro,Manning Joseph C.,Tekgüç Hakan,

Abstract

Abstract Background Management and monitoring of pain and sedation to reduce discomfort as well as side effects, such as over- and under-sedation, withdrawal syndrome and delirium, is an integral part of pediatric intensive care practice. However, the current state of management and monitoring of analgosedation across European pediatric intensive care units (PICUs) remains unknown. The aim of this survey was to describe current practices across European PICUs regarding the management and monitoring of pain and sedation. Methods An online survey was distributed among 357 European PICUs assessing demographic features, drug choices and dosing, as well as usage of instruments for monitoring pain and sedation. We also compared low- and high-volume PICUs practices. Responses were collected from January to April 2021. Results A total of 215 (60% response rate) PICUs from 27 European countries responded. Seventy-one percent of PICUs stated to use protocols for analgosedation management, more frequently in low-volume PICUs (77% vs 63%, p = 0.028). First-choice drug combination was an opioid with a benzodiazepine, namely fentanyl (51%) and midazolam (71%) being the preferred drugs. The starting doses differed between PICUs from 0.1 to 5 mcg/kg/h for fentanyl, and 0.01 to 0.5 mg/kg/h for midazolam. Daily assessment and documentation for pain (81%) and sedation (87%) was reported by most of the PICUs, using the preferred validated FLACC scale (54%) and the COMFORT Behavioural scale (48%), respectively. Both analgesia and sedation were mainly monitored by nurses (92% and 84%, respectively). Eighty-six percent of the responding PICUs stated to use neuromuscular blocking agents in some scenarios. Monitoring of paralysed patients was preferably done by observation of vital signs with electronic devices support. Conclusions This survey provides an overview of current analgosedation practices among European PICUs. Drugs of choice, dosing and assessment strategies were shown to differ widely. Further research and development of evidence-based guidelines for optimal drug dosing and analgosedation assessment are needed.

Publisher

Springer Science and Business Media LLC

Subject

Critical Care and Intensive Care Medicine

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