Evidence map›Paper›PMID 32627176›Full record

ArticleBiometrics2021

A Bayesian hierarchical model for characterizing the diffusion of new antipsychotic drugs.

Chenyang Gu, Haiden Huskamp, Julie Donohue, Sharon-Lise Normand

Open access · greenAbstract read
In one paragraph

Article in Biometrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 91% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Chenyang GuHarvard Medical School, Analysis Group, Inc., Los Angeles, California.
Haiden HuskampDepartment of Health Care Policy, Harvard Medical School, Boston, Massachusetts.
Julie DonohueDepartment of Health Policy and Management, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
Sharon-Lise NormandDepartment of Health Care Policy, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0001-7027-4769
Harvard University · USUniversity of Pittsburgh · US

Funding

Technology Diffusion PathwaysU01MH103018 · NIMH · HARVARD MEDICAL SCHOOL · PI HUSKAMP, HAIDEN A., NORMAND, SHARON-LISE TERESA · 2013 to 2017
$2.7M
Improving Value of Publicly Funded Mental Health CareR01MH106682 · NIMH · RAND CORPORATION · PI HORVITZ-LENNON, MARCELA V, NORMAND, SHARON-LISE TERESA · 2016 to 2019
$2.6M
Influences on Psychiatrist Prescribing of AntipsychoticsR01MH093359 · NIMH · HARVARD MEDICAL SCHOOL · PI DONOHUE, JULIE MARIE, HUSKAMP, HAIDEN A. · 2012 to 2014
$1.6M
THE MDEPINET MEDICAL COUNTER MEASURES STUDYU01FD004493 · FDA · HARVARD MEDICAL SCHOOL · PI NORMAND, SHARON-LISE TERESA, RESNIC, FREDERIC S · 2012 to 2012
$1.6M
FDA HHS U01 FD004493NIMH NIH HHS R01 MH093359NIMH NIH HHS R01 MH106682NIMH NIH HHS U01 MH103018NIMH NIH HHS U01-MH103018
6 · The paper itself

Abstract

New prescription medications are a primary driver of spending growth in the United States. For patients with severe mental illnesses, second-generation antipsychotic (SGA) medications feature prominently. However, many SGAs are costly, particularly before generic entry, and some may increase the risk of diabetes. Because physicians play a prominent role in new prescription adoption, understanding their prescribing behaviors is policy-relevant. Several features of prescription data, such as different antipsychotic choice sets over time, variable physician prescription volumes, and correlation among drug choices within physicians, complicate inferences. We propose a multivariate Bayesian hierarchical model with piecewise random effects to characterize the diffusion of new antipsychotic drugs. This model captures the complex prescriber-specific relationships among the different diffusion processes and takes advantage of the Bayesian paradigm to quantify uncertainty for all parameters straightforwardly. To evaluate the prescribing patterns for each physician, we propose various indices to identify early new SGA adopters. A sample of nearly 17,000 US physicians whose antipsychotic drug prescribing information was collected between January 1, 1997 and December 31, 2007 illustrates the methods. Determinants of high prescription rates and adoption speeds of new SGAs included physician sex, age, hospital affiliation, physician specialty, and office location. Large within- and between-provider variations in prescribing patterns of new SGAs were identified. Early adopters for one drug were not early adopters for another drug.

Indexed as

Antipsychotic AgentsMental DisordersBayes TheoremDrug PrescriptionsHumansPractice Patterns, Physicians'United StatesAntipsychotic Agentsadoption speedmultivariate Poisson regressionpiecewise random effectsprofiling

Identifiers

PMID32627176
PMCPMC8108482
OpenAlexW3040201935

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.