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Interpretation and management of INR results: a case history based survey in 13 countries
Ann-Helen Kristoffersen1, Geir Thue, Eva Ajzner
1Laboratory of Clinical Biochemistry, Haukeland University Hospital, Helse Bergen HF, Bergen, Norway. ann.kristoffersen@helse-bergen.no
Insights
Vitamin K antagonist (VKA) treatment monitoring shows significant variation among physicians globally. This lack of standardization in VKA management may lead to clinical consequences, necessitating improved guidelines.
Area of Science:
- Cardiology
- Pharmacology
- Internal Medicine
Background:
- Standardization of treatment with vitamin K antagonists (VKAs) remains a challenge despite their long-standing use.
- Existing VKA monitoring practices in primary and secondary care require exploration to identify areas for improvement.
Purpose of the Study:
- To investigate physician practices regarding VKA monitoring in both primary and secondary care settings.
- To identify variations in VKA management and their potential clinical implications.
Main Methods:
- Distribution of two case histories (stable anticoagulation and supratherapeutic INR) to physicians across 13 countries.
- Inquiry into INR measurement frequency, VKA dose adjustment thresholds, and perceived risks of stroke and bleeding.
- Analysis of responses from 3016 physicians, predominantly from primary care.
Main Results:
- Substantial variation in VKA monitoring practices observed within and between countries, irrespective of care level or VKA type.
- Physicians frequently overestimated ischemic stroke and bleeding risks by 2-3 times.
- Significant discrepancies in VKA dose reduction and timing of repeat INR measurements were noted, particularly in cases of supratherapeutic INR.
Conclusions:
- Widespread variation in VKA monitoring indicates significant clinical consequences.
- Current guidelines for VKA management may be inadequately known or perceived as impractical.
- Enhanced efforts are crucial to standardize VKA management and improve patient outcomes.
Introduction:
Standardisation of treatment with vitamin K antagonists (VKAs) is still an issue after 60 years of use. The study aimed to explore aspects of VKA monitoring in primary and secondary care.
Methods:
Two case histories were distributed to physicians in 13 countries. Case history A focused on a patient with atrial fibrillation on stable anticoagulation (latest INR 2.3). Physicians were asked about frequency of INR measurement, when to change the VKA dose, and the patient's annual risk of ischemic stroke and bleeding. Case history B focused on a patient with an unexpected INR of 4.8, asking for the patient's 48-hour bleeding risk, the immediate dose reduction and time until a repeat INR.
Results:
Altogether, 3016 physicians responded (response rate 8 - 38%), of which 82% were from primary care and 18% from secondary care. Answers varied substantially within and between countries regardless of level of care and VKA used. Median number of weeks between INR measurements was 4 - 6 weeks. Median threshold INR for increasing or decreasing the VKA dose was 1.9 and 3.1, respectively. Risk of ischemic stroke and bleeding were overestimated 2 - 3 times. In case history B, the median dose reduction the two first days was 75% for GPs and 55% for specialists, irrespective of estimates of bleeding risk; with one week to a repeat INR.
Conclusion:
Variation in VKA monitoring is substantial implying clinical consequences. Guidelines seem either unknown or may be considered impracticable. Further efforts towards standardisation of VKA management are needed.
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