Abstract
Dysphagia occurs commonly in the intensive care unit (ICU). Despite the clinical relevance, there is little worldwide research on prevention, assessment, evaluation, and/or treatment of dysphagia for ICU patients. We aimed to gain insight into this international knowledge gap. We conducted a multi-center, international online cross-sectional survey of adult ICUs. Local survey distribution champions were recruited through professional and personal networks. The survey was administered from November 2017 to June 2019 with three emails and a final telephone reminder. Responses were received from 746 ICUs (26 countries). In patients intubated > 48 h, 17% expected a > 50% chance that dysphagia would develop. This proportion increased to 43% in patients intubated > 7 days, and to 52% in tracheotomized patients. Speech-language pathologist (SLP) consultation was available in 66% of ICUs, only 4% reported a dedicated SLP. Although 66% considered a routine post-extubation dysphagia protocol important, most (67%) did not have a protocol. Few ICUs routinely assessed for dysphagia after 48 h of intubation (30%) or tracheostomy (41%). A large proportion (46%) used water swallow screening tests to determine aspiration, few (8%) used instrumental assessments (i.e., flexible endoscopic evaluation of swallowing). Swallowing exercises were used for dysphagia management by 30% of ICUs. There seems to be limited awareness among ICU practitioners that patients are at risk of dysphagia, particularly as ventilation persists, protocols, routine assessment, and instrumental assessments are generally not used. We recommend the development of a research agenda to increase the quality of evidence and ameliorate the implementation of evidence-based dysphagia protocols by dedicated SLPs.
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Abbreviations
- ICU:
-
Intensive care unit
- FEES:
-
Flexible endoscopic evaluation of swallowing
- NEMS:
-
Neuromuscular electrical stimulation
- PES:
-
Pharyngeal electrical stimulation
- PEG:
-
Percutaneous endoscopic gastrostomy
- SD:
-
Standard deviation
- sEMG:
-
Surface electromyography
- SLP:
-
Speech-language pathologist
- VFSS:
-
Videofluoroscopic swallowing study
- V-VST:
-
Volume–viscosity swallow test
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Acknowlegments
Co-authors of DICE study investigator group
Survey development team: M. B. Brodsky (Johns Hopkins University, Baltimore, USA); L. Rose (King’s College London, London, UK); J. Lut (Gelre Hospitals, Apeldoorn, The Netherlands); P. Clavé (Hospital de Mataró, Universitat Autónoma de Barcelona, Centro de Investigación Biomédica en Red de Enfermedades Aparato DIgestivo, Ciberehd Barcelona, Spain); R. Nanchal (Medical college Wisconsin, USA); Y. Inamoto (Fujita Health University, Aichi, Japan); J. I. van der Hoeven (Radboud University, Nijmegen, The Netherlands); P. E. Spronk (Gelre Hospitals, Apeldoorn, The Netherlands). National study coordinators: A. Freeman-Sanderson (Australia); M. Hiesmayr, C. Veraar (Austria); C. E. Hickmann, R. Gosselink (Belgium); L. Rose, S. Gershman, S. Skoretz, R. Martino (Canada); M. Mpouzika (Cyprus); M. Cerny, V. Chrobok, L. Zeinerova (Czech Republic); I. Egerod, G. Kaldan (Denmark); J. McRae (England); M. Bäcklund (Finland); T. Ramos (France); P. Nydahl (Germany); M. Kalafati (Greece); T. Andrews (Ireland); R. Sperlinga (Italy); H. Katsukawa, F. Kasai (Japan); P. E. Spronk, J. Lut, L. E. J. Spronk (Netherlands); A. Miles (New Zealand); J. McGaughey, S. Duncan (Northern Ireland (UK)); M. Fossum, V. Ágústdóttir, T. Senneset, M. Larsson, G. Hammond (Norway); R. Owczuk (Poland); S. Mestre (Portugal); J. Merriweather (Scotland); M. Tedla, Z. Frajkova (Slovakia); M. Velasco (Spain); E. Akerman (Sweden); A. Sibilla, B. Kertscher, B. Gaechter (Switzerland); S. Serel Arslan, N. Demir (Turkey); G. Jones (Wales).
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This study was partially funded by the Gelre Hospitals science fund (Grant 2018-012).
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All authors of the DICE study investigator group contributed substantially to the conception and design of the study, the acquisition of data, or the analysis and interpretation of the data. All authors of the DICE study investigator group drafted or provided critical revision of the article and provided their final approval of the version submitted for publication. In more detail, material preparation, data collection, and analysis were done by LEJS, JL, and PES. PES drafted the manuscript and members of the writing group (LEJS, MBB, LR, IE, JM, and JM) revised it critically for important intellectual content. Subsequently, the version was distributed among all the other DICE study group investigators for critical appraisal. All authors mentioned as national study coordinators participated in ethical approvals, recruitment, and data collection in their respective countries. See non-anonymized version.
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Research ethics approval for survey conduct was obtained according to the requirements of each country by national study coordinators. Written confirmation of ethics approval, or the confirmation that requirements were waived, was obtained by the study investigator (Peter E. Spronk) from all national study coordinators prior to data collection. A paragraph mentioning this information was added to the methods section of the manuscript.
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Returning a survey was indicating consent to participate in this survey by national coordinators who were responsible for contacts with the ICUs in their country/region. The ICUs were allowed to opt out of study participation, but this never occurred.
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Spronk, P.E., Spronk, L.E.J., Egerod, I. et al. Dysphagia in Intensive Care Evaluation (DICE): An International Cross-Sectional Survey. Dysphagia 37, 1451–1460 (2022). https://doi.org/10.1007/s00455-021-10389-y
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DOI: https://doi.org/10.1007/s00455-021-10389-y