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Evaluating opioid analgesic prescribing limits: A narrative review
Amy E Seitz1, Karen A Janiszewski1, Gery P Guy2
1Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, Maryland, USA.
Opioid prescribing limits decreased opioid analgesic use, but evidence on patient health outcomes remains limited. Future research should assess unintended consequences of these opioid policies.
Area of Science:
- Public Health
- Health Policy
- Pharmacology
Background:
- The opioid crisis has led to widespread implementation of opioid analgesic guidelines and prescribing limits.
- These regulations aim to control opioid prescribing and mitigate public health risks.
Purpose of the Study:
- To review evidence on the patient and public health impact of federal and state opioid analgesic prescribing guidelines and laws.
- To identify research gaps and challenges in evaluating these policies.
- To suggest future research directions for assessing policy impacts and unintended consequences.
Main Methods:
- A narrative review of literature published between 2013 and 2019.
- Analysis of 30 studies examining opioid analgesic thresholds and policies, including federal guidelines, state laws, and Medicaid plans.
- Focus on studies evaluating interventions like prior authorization.
Main Results:
- Most studies reported decreases in opioid analgesic prescribing and dispensing following policy implementation.
- Limited research evaluated patient or public health outcomes beyond prescribing patterns.
- Few studies stratified results by sociodemographic or clinical factors, and none assessed potential adverse patient outcomes.
Conclusions:
- Significant knowledge gaps exist regarding the comprehensive impact of opioid analgesic prescribing regulations.
- Further research is needed to adequately assess the effects and unintended consequences of these policies.
- Future studies should focus on patient-centered outcomes and potential harms.
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