Please use this identifier to cite or link to this item:
https://ahro.austin.org.au/austinjspui/handle/1/13126
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Hart, Graeme K | en |
dc.contributor.author | Baldwin, Ian C | en |
dc.contributor.author | Gutteridge, Geoffrey A | en |
dc.contributor.author | Ford, J | en |
dc.date.accessioned | 2015-05-16T02:54:41Z | |
dc.date.available | 2015-05-16T02:54:41Z | |
dc.date.issued | 1994-10-01 | en |
dc.identifier.citation | Anaesthesia and Intensive Care; 22(5): 556-61 | en |
dc.identifier.govdoc | 7818059 | en |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/13126 | en |
dc.description.abstract | This prospective, observational, anonymous incident reporting study aimed to identify and correct factors leading to reduced patient safety in intensive care. An incident was any event which caused or had the potential to cause harm to the patient, but included problems in policy or procedure. Reports were discussed at monthly meetings. Of 390 incidents, 106 occasioned "actual" harm and 284 "potential" harm. There was one death, 86 severe complications and 88 complications of minor severity. Most were transient but the effects of 24 lasted up to a week. Most incidents affected cardiovascular and respiratory systems. Incident categories involved drugs, equipment, management or procedures. Incident causes were knowledge-based, rule-based, technical, slip/lapse, no error or unclassifiable. The study has identified some human and equipment performance problems in our intensive care unit. Correction of these should lead to a reduction in the future incidence of those events and hence an increased level of patient safety. | en |
dc.language.iso | en | en |
dc.subject.other | Accidents.statistics & numerical data | en |
dc.subject.other | Adult | en |
dc.subject.other | Bed Occupancy.statistics & numerical data | en |
dc.subject.other | Cause of Death | en |
dc.subject.other | Drug-Related Side Effects and Adverse Reactions | en |
dc.subject.other | Equipment Failure | en |
dc.subject.other | Equipment and Supplies, Hospital | en |
dc.subject.other | Hospital Administration | en |
dc.subject.other | Hospital Information Systems | en |
dc.subject.other | Humans | en |
dc.subject.other | Intensive Care.organization & administration.statistics & numerical data | en |
dc.subject.other | Intensive Care Units.organization & administration.statistics & numerical data | en |
dc.subject.other | Patient Admission.statistics & numerical data | en |
dc.subject.other | Pilot Projects | en |
dc.subject.other | Policy Making | en |
dc.subject.other | Process Assessment (Health Care) | en |
dc.subject.other | Prospective Studies | en |
dc.subject.other | Risk Factors | en |
dc.subject.other | Safety | en |
dc.subject.other | Victoria.epidemiology | en |
dc.title | Adverse incident reporting in intensive care. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | Anaesthesia and Intensive Care | en |
dc.identifier.affiliation | Intensive Care Unit, Austin Hospital, Heidelberg, Victoria. | en |
dc.description.pages | 556-61 | en |
dc.relation.url | https://pubmed.ncbi.nlm.nih.gov/7818059 | en |
dc.type.austin | Journal Article | en |
local.name.researcher | Baldwin, Ian C | |
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 | - |
crisitem.author.dept | Intensive Care | - |
Appears in Collections: | Journal articles |
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