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. 2014 May 7;9(5):e96990.
doi: 10.1371/journal.pone.0096990. eCollection 2014.

Real-world efficiency of pharmacogenetic screening for carbamazepine-induced severe cutaneous adverse reactions

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Real-world efficiency of pharmacogenetic screening for carbamazepine-induced severe cutaneous adverse reactions

Zhibin Chen et al. PLoS One. .

Abstract

Objectives: We evaluated the cost and efficiency of routine HLA-B*15 ∶ 02 screening to prevent carbamazepine-induced Stevens-Johnson syndrome and toxic epidermal necrolysis (CBZ-SJS/TEN) in Hong Kong.

Methods: Data were extracted from patients who commenced CBZ as the first-ever AED treatment or tested for HLA-B*15 ∶ 02 allele in three years before policy implementation (pre-policy: 16 September 2005 to 15 September 2008) and three years after (post-policy: 16 September 2008 to 15 September 2011). Using published unit costs, we estimated the cost of screening by comparing the costs to prevent and treat CBZ-SJS/TEN. We compared the number of person-tests needed and the cost to prevent resultant death with cancer screening programs.

Results: The number of screening tests needed to prevent one case of CBZ-SJS/TEN was 442, and to prevent one resultant death was 1,474 to 8,840. The screening cost was $332 per person, of which 42% was attributed to an additional consultation to review result and prescribe appropriate medication. HLA-B*15 ∶ 02 screening expended $146,749 to prevent a case of CBZ-SJS/TEN, and $489,386- $2,934,986 to prevent a resultant death. The corresponding numbers of tests and costs for mammography and Pap smear to prevent death due to breast and cervical cancers were 7,150 and 7,000, and $614,900 and $273,000, respectively. Comparing to the SJS/TEN treatment cost, HLA-B*15 ∶ 02 screening would become cost saving if a point-of-care test of less than $37 was available.

Conclusions: HLA-B*15 ∶ 02 screening is as efficient as mammography and Pap smear in preventing death. Development of point-of-care testing will vastly improve efficiency.

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Conflict of interest statement

Competing Interests: The authors have read the journal’s policy and have the following conflicts: PK has received research grants from the US National Institutes of Health, Hong Kong Research Grants Council, Innovation and Technology Fund, and Health and Health Services Research Fund. He/his institution also received speaker’s or consultancy fees and/or research grants from Eisai, GlaxoSmithKline, Johnson & Johnson, Pfizer, and UCB Pharma; DL has received research grants from the National Health and Medical Research Council of Australia, the Australian Research Council and the National Heart Foundation of Australia. He/his institution has also received speaker’s or consultancy fees and/or research grants from Pfizer, Abbvie, Sanofi, AstraZeneca, GlaxoSmithKline and Amgen; no other relationships or activities that could appear to have influenced the submitted work. No support from any organisation for the submitted work. This does not alter the authors’ adherence to PLOS ONE policies on sharing data and materials.

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