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https://ahro.austin.org.au/austinjspui/handle/1/30524
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DC Field | Value | Language |
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dc.contributor.author | Levkovich, Bianca J | - |
dc.contributor.author | Orosz, Judit | - |
dc.contributor.author | Bingham, Gordon | - |
dc.contributor.author | Cooper, D James | - |
dc.contributor.author | Dooley, Michael | - |
dc.contributor.author | Kirkpatrick, Carl | - |
dc.contributor.author | Jones, Daryl A | - |
dc.date | 2022 | - |
dc.date.accessioned | 2022-07-14T13:03:48Z | - |
dc.date.available | 2022-07-14T13:03:48Z | - |
dc.date.issued | 2023-04 | - |
dc.identifier.citation | BMJ Quality & Safety 2023; 32(4) | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/30524 | - |
dc.description.abstract | Despite recognition of clinical deterioration and medication-related harm as patient safety risks, the frequency of medication-related Rapid Response System activations is undefined. We aimed to estimate the incidence and preventability of medication-related Medical Emergency Team (MET) activations and describe the associated adverse medication events. A case review study of consecutive MET activations at two acute, academic teaching hospitals in Melbourne, Australia with mature Rapid Response Systems was conducted. All MET activations during a 3-week study period were assessed for a medication cause including identification of the contributing adverse medication event and its preventability, using validated tools and recognised classification systems. There were 9439 admissions and 628 MET activations during the study period. Of these, 146 (23.2%) MET activations were medication related: an incidence of 15.5 medication-related MET activation per 1000 admissions. Medication-related MET activations occurred a median of 46.6 hours earlier (IQR 22-165) in an admission than non-medication-related activations (p=0.001). Furthermore, this group also had more repeat MET activations during their admission (p=0.021, OR=1.68, 95% CI 1.09 to 2.59). A total of 92 of 146 (63%) medication-related MET activations were potentially preventable. Tachycardia due to omission of beta-blocking agents (10.9%, n=10 of 92) and hypotension due to cumulative toxicity (9.8%, n=9 of 92) or inappropriate use (10.9%, n=10 of 92) of antihypertensives were the most common adverse medication events leading to potentially preventable medication-related MET activations. Medications contributed to almost a quarter of MET activations, often early in a patient's admission. One in seven MET activations were due to potentially preventable adverse medication events. The most common of these were omission of beta-blockers and clinically inappropriate antihypertensive use. Strategies to prevent these events would increase patient safety and reduce burden on the MET. | en |
dc.language.iso | eng | - |
dc.subject | Adverse events, epidemiology and detection | en |
dc.subject | Hospital medicine | en |
dc.subject | Medical emergency team | en |
dc.subject | Medication safety | en |
dc.subject | Patient safety | en |
dc.title | Medication-related Medical Emergency Team activations: a case review study of frequency and preventability. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | BMJ quality & safety | en |
dc.identifier.affiliation | Intensive Care | en |
dc.identifier.affiliation | Centre for Medicines Use and Safety, Monash University, Clayton, Victoria, Australia.. | en |
dc.identifier.affiliation | Department of Intensive Care and Hyperbaric Medicine, The Alfred, Melbourne, Victoria, Australia.. | en |
dc.identifier.affiliation | Alfred Health, Melbourne, Victoria, Australia.. | en |
dc.identifier.affiliation | Australia and New Zealand Intensive Care Research Centre, Monash University, Clayton, Victoria, Australia.. | en |
dc.identifier.affiliation | Centre for Medicines Use and Safety, Monash University, Clayton, Victoria, Australia.. | en |
dc.identifier.affiliation | Pharmacy, Alfred Health, Melbourne, Victoria, Australia.. | en |
dc.identifier.pubmeduri | https://pubmed.ncbi.nlm.nih.gov/35790383/ | en |
dc.identifier.doi | 10.1136/bmjqs-2021-014185 | en |
dc.type.content | Text | en |
dc.identifier.orcid | http://orcid.org/0000-0002-2693-2944 | en |
dc.identifier.orcid | http://orcid.org/0000-0002-3440-1289 | en |
dc.identifier.orcid | http://orcid.org/0000-0002-5872-9051 | en |
dc.identifier.orcid | http://orcid.org/0000-0002-5715-1534 | en |
dc.identifier.orcid | http://orcid.org/0000-0002-6446-3595 | en |
dc.identifier.pubmedid | 35790383 | - |
local.name.researcher | Jones, Daryl A | |
item.openairetype | Journal Article | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | Intensive Care | - |
Appears in Collections: | Journal articles |
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