2017
DOI: 10.1016/j.jval.2017.06.007
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Comparing Methods for Estimating Direct Costs of Adverse Drug Events

Abstract: The estimated costs resulting from ADEs varied considerably depending on the methodological choices. The results indicate that costs for ADEs need to be identified through medical record review and by using detailed unit cost data.

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Cited by 7 publications
(9 citation statements)
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“… 10 The cost evaluation method employed was the resource use method. 29 The reviewers were instructed that the ADE contributing the most to costs should be listed first. If the first ADE listed by a reviewer was an ADR, any additional ADEs contributing to the resource use during that same healthcare encounter could potentially contribute to an overestimation of cost.…”
Section: Discussionmentioning
confidence: 99%
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“… 10 The cost evaluation method employed was the resource use method. 29 The reviewers were instructed that the ADE contributing the most to costs should be listed first. If the first ADE listed by a reviewer was an ADR, any additional ADEs contributing to the resource use during that same healthcare encounter could potentially contribute to an overestimation of cost.…”
Section: Discussionmentioning
confidence: 99%
“… 29 Costs assessed as dominantly caused by an ADR can be expected to better represent the actual costs to the health system. 29 The analyses in this article are descriptive in nature, and the results were not adjusted for other factors, such as comorbidities. Thus, methods for estimating the attributable costs of ADRs were not used, such as adjusted regression analyses or propensity score matching, due to residual confounding limiting the comparability of groups.…”
Section: Discussionmentioning
confidence: 99%
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“…Notwithstanding all the benefits of small molecule drugs, it remains the case that they are also widely associated with various morbidities and mortalities, often referred to as “adverse drug reactions” (ADRs) (e.g., [ 326 , 327 , 328 , 329 , 330 , 331 , 332 , 333 , 334 , 335 , 336 , 337 , 338 , 339 , 340 , 341 , 342 , 343 , 344 , 345 , 346 ]). Despite the lengthy and complex regulatory hurdles that drugs must overcome before being marketed (and toxicity remains a major cause of so-called “attrition” where drug candidates are pulled before they even get to market [ 347 , 348 , 349 , 350 , 351 , 352 , 353 ]), ADRs are extremely common (and hard to anticipate, given the huge genetic and phenotypic variation in human populations [ 354 ]).…”
Section: Introductionmentioning
confidence: 99%