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https://ahro.austin.org.au/austinjspui/handle/1/17500
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Campbell, Craig A | - |
dc.contributor.author | Lam, Que T | - |
dc.contributor.author | Horvath, Andrea R | - |
dc.date | 2018-04-19 | - |
dc.date.accessioned | 2018-04-24T05:33:15Z | - |
dc.date.available | 2018-04-24T05:33:15Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Clinical chemistry and laboratory medicine 2018; 57(1): 89-94 | - |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/17500 | - |
dc.description.abstract | Individual laboratories are required to compose an alert list for identifying critical and significant risk results. The high-risk result working party of the Royal College of Pathologists of Australasia (RCPA) and the Australasian Association of Clinical Biochemists (AACB) has developed a risk-based approach for a harmonized alert list for laboratories throughout Australia and New Zealand. The six-step process for alert threshold identification and assessment involves reviewing the literature, rating the available evidence, performing a risk analysis, assessing method transferability, considering workload implications and seeking endorsement from stakeholders. To demonstrate this approach, a worked example for deciding the upper alert threshold for potassium is described. The findings of the worked example are for infants aged 0-6 months, a recommended upper potassium alert threshold of >7.0 mmol/L in serum and >6.5 mmol/L in plasma, and for individuals older than 6 months, a threshold of >6.2 mmol/L in both serum and plasma. Limitations in defining alert thresholds include the lack of well-designed studies that measure the relationship between high-risk results and patient outcomes or the benefits of treatment to prevent harm, and the existence of a wide range of clinical practice guidelines with conflicting decision points at which treatment is required. The risk-based approach described presents a transparent, evidence- and consensus-based methodology that can be used by any laboratory when designing an alert list for local use. The RCPA-AACB harmonized alert list serves as a starter set for further local adaptation or adoption after consultation with clinical users. | - |
dc.language.iso | eng | - |
dc.subject | alert list | - |
dc.subject | alert threshold | - |
dc.subject | critical result | - |
dc.subject | critical risk result | - |
dc.subject | harmonization | - |
dc.subject | hyperkalemia | - |
dc.title | An evidence- and risk-based approach to a harmonized laboratory alert list in Australia and New Zealand. | - |
dc.type | Journal Article | - |
dc.identifier.journaltitle | Clinical chemistry and laboratory medicine | - |
dc.identifier.affiliation | NSW Health Pathology, Department of Clinical Chemistry and Endocrinology, Prince of Wales Hospital, Sydney, NSW 2031, Australia | - |
dc.identifier.affiliation | Australian Institute of Health Innovation, Macquarie University, Sydney, NSW, Australia | - |
dc.identifier.affiliation | Department of Pathology, Austin Health, Heidelberg, Victoria, Australia | - |
dc.identifier.affiliation | NSW Health Pathology, Department of Clinical Chemistry and Endocrinology, Prince of Wales Hospital, Sydney, NSW, Australia | - |
dc.identifier.doi | 10.1515/cclm-2017-1114 | - |
dc.identifier.pubmedid | 29672264 | - |
dc.type.austin | Journal Article | - |
local.name.researcher | Lam, Que T | |
item.grantfulltext | none | - |
item.openairetype | Journal Article | - |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Pathology | - |
Appears in Collections: | Journal articles |
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