Evidence map›Paper›PMID 24313239›Full record

ArticleThe American journal on addictions

Effects of HCV seropositive status on buprenorphine pharmacokinetics in opioid-dependent individuals.

Carmen L Masson, Petrie M Rainey, David E Moody, Elinore F McCance-Katz

Open access · greenAbstract read
In one paragraph

Article in The American journal on addictions. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Buprenorphine-cannabis interaction in patients undergoing opioid maintenance therapy.European archives of psychiatry and clinical neuroscience · 2021
    Article
  3. Review
  4. Article
  5. 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 3 institutions in 1 country.

Carmen L MassonDepartment of Psychiatry, University of California, San Francisco, California.
Petrie M Rainey
David E Moody
Elinore F McCance-Katz
University of California, San Francisco · USUniversity of Utah · USUniversity of Washington · US

Funding

TREATMENTS FOR COMPLEX PATIENTS IN NEW SETTINGSP50DA009253 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GUYDISH, JOSEPH R · 1994 to 2014
$28.2M
Western States Node of the National Drug Abuse Treatment Clinical Trials NetworkU10DA015815 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MCCARTY, DENNIS, SORENSEN, JAMES L · 2002 to 2015
$25.2M
Western States Node of the National Drug Abuse Treatment Clinical Trials Network (TMS for CUD) UG1DA015815 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Keith N. Humphreys, Philip Todd Korthuis · 2015 to 2026
$24.6M
Opioids &HIV Medications: Interactions in Drug AbusersR01DA013004 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI MCCANCE-KATZ, ELINORE F. · 1999 to 2008
$4.9M
Hepatitis Care Coordination in Methadone TreatmentR01DA020781 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MASSON, CARMEN L · 2006 to 2010
$1.7M
Role of Buprenorphine in Improving Clinical Care in Opioid Addiction and HIVK24DA023359 · NIDA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MCCANCE-KATZ, ELINORE F. · 2007 to 2011
$918k
Human Metabolism of Anti-Abuse MedicationsR01DA010100 · NIDA · UNIVERSITY OF UTAH · PI MOODY, DAVID E · 1997 to 2005
$750k
NIDA NIH HHS K24 DA023359NIDA NIH HHS P50 DA009253NIDA NIH HHS R01 DA010100NIDA NIH HHS R01 DA013004NIDA NIH HHS R01 DA020781NIDA NIH HHS R01 DA10100NIDA NIH HHS R01 DA13004NIDA NIH HHS U10 DA015815NIDA NIH HHS UG1 DA015815NIMHD NIH HHS L60 MD003097
6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe purpose of this study was to examine the effect of hepatitis C virus (HCV) infection on buprenorphine pharmacokinetics in opioid-dependent, buprenorphine/naloxone-maintained adults.

methodsA retrospective analysis of buprenorphine pharmacokinetics in HCV seropositive and seronegative buprenorphine/naloxone-maintained individuals (N = 49) was undertaken.

resultsRelative to HCV seronegative subjects, HCV seropositive subjects had higher buprenorphine exposure, as demonstrated by elevated buprenorphine AUC and Cmax values (p = .03 and .02, respectively) and corresponding elevations in the metabolites, buprenorphine-3-glucuronide AUC values (p = .03) and norbuprenorphine-3-glucuronide AUC and C24 values (p = .05 and .03, respectively). DISCUSSION AND

conclusionsHCV infection was associated with higher plasma concentrations of buprenorphine and buprenorphine metabolites. SCIENTIFIC SIGNIFICANCE AND FUTURE DIRECTIONS: Findings suggest the potential for opioid toxicity among HCV-infected patients treated with buprenorphine/naloxone, and possible hepatotoxic effects related to increased buprenorphine exposure. HCV-infected patients receiving buprenorphine may need lower doses to maintain therapeutic plasma concentrations.

Indexed as

AdultBuprenorphineCase-Control StudiesFemaleHepatitis CHepatitis C AntibodiesHumansMaleNaloxoneNarcotic AntagonistsOpioid-Related DisordersRetrospective StudiesYoung AdultBuprenorphineHepatitis C AntibodiesNaloxoneNarcotic Antagonists

Identifiers

PMID24313239
PMCPMC3998818
OpenAlexW2152731932

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.