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1.
J Gen Intern Med ; 23(9): 1393-8, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18592319

ABSTRACT

BACKGROUND: Buprenorphine is a safe, effective and underutilized treatment for opioid dependence that requires special credentialing, known as a waiver, to prescribe in the United States. OBJECTIVE: To describe buprenorphine clinical practices and barriers among office-based physicians. DESIGN: Cross-sectional survey. PARTICIPANTS: Two hundred thirty-five office-based physicians waivered to prescribe buprenorphine in Massachusetts. MEASUREMENTS: Questionnaires mailed to all waivered physicians in Massachusetts in October and November 2005 included questions on medical specialty, practice setting, clinical practices, and barriers to prescribing. Logistic regression analyses were used to identify factors associated with prescribing. RESULTS: Prescribers were 66% of respondents and prescribed to a median of ten patients. Clinical practices included mandatory counseling (79%), drug screening (82%), observed induction (57%), linkage to methadone maintenance (40%), and storing buprenorphine notes separate from other medical records (33%). Most non-prescribers (54%) reported they would prescribe if barriers were reduced. Being a primary care physician compared to a psychiatrist (AOR: 3.02; 95% CI: 1.48-6.18) and solo practice only compared to group practice (AOR: 3.01; 95% CI: 1.23-7.35) were associated with prescribing, while reporting low patient demand (AOR: 0.043, 95% CI: 0.009-0.21) and insufficient institutional support (AOR: 0.37; 95% CI: 0.15-0.89) were associated with not prescribing. CONCLUSIONS: Capacity for increased buprenorphine prescribing exists among physicians who have already obtained a waiver to prescribe. Increased efforts to link waivered physicians with opioid-dependent patients and initiatives to improve institutional support may mitigate barriers to buprenorphine treatment. Several guideline-driven practices have been widely adopted, such as adjunctive counseling and monitoring patients with drug screening.


Subject(s)
Buprenorphine/therapeutic use , Narcotic Antagonists/therapeutic use , Opioid-Related Disorders/drug therapy , Practice Patterns, Physicians' , Cross-Sectional Studies , Data Collection , Humans , Massachusetts , Physicians, Family , Private Practice , Psychiatry
2.
J Acquir Immune Defic Syndr ; 46(2): 194-9, 2007 Oct 01.
Article in English | MEDLINE | ID: mdl-17667330

ABSTRACT

OBJECTIVE: To assess the relation between alcohol consumption and laboratory markers of HIV disease progression. METHODS: We prospectively assessed CD4 cell counts, HIV RNA levels, and alcohol consumption for up to 7 years in 595 HIV-infected persons with alcohol problems recruited between 1997 and 2003. We investigated the relation of these markers of HIV disease progression to alcohol consumption using longitudinal regression models controlling for known prognostic factors, including adherence and depressive symptoms, and stratified by antiretroviral therapy (ART) use. RESULTS: Among subjects who were not on ART, heavy alcohol consumption was associated with a lower CD4 cell count (adjusted mean decrease of 48.6 cells/microL compared with abstinence; P = 0.03) but not with higher log(10) HIV RNA. Among subjects who were on ART, heavy alcohol consumption was not associated with a lower CD4 cell count or higher log(10) HIV RNA. CONCLUSIONS: Heavy alcohol consumption has a negative impact on the CD4 cell count in HIV-infected persons not receiving ART. In addition to the known deleterious effects of alcohol on ART adherence, these findings suggest that avoiding heavy alcohol consumption in patients not on ART may have a beneficial effect on HIV disease progression.


Subject(s)
Alcohol Drinking , HIV Infections/diagnosis , HIV-1 , Adult , Anti-HIV Agents/therapeutic use , CD4 Lymphocyte Count , Cohort Studies , Disease Progression , Female , HIV Infections/drug therapy , HIV Infections/immunology , HIV Infections/virology , HIV-1/genetics , HIV-1/isolation & purification , Humans , Male , Patient Compliance , Prospective Studies , RNA, Viral/analysis , Treatment Outcome
3.
J Gen Intern Med ; 22(6): 822-5, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17503108

ABSTRACT

BACKGROUND AND OBJECTIVE: It is unknown whether testing HIV-infected individuals for hepatitis C virus (HCV) and informing them of their HCV status impacts subsequent alcohol use. We hypothesized that HIV-infected individuals with current or past alcohol problems who reported being told they had HCV were more likely to 1) abstain from alcohol and 2) not drink unhealthy amounts compared to individuals who had not been told. DESIGN, PARTICIPANTS, AND MEASUREMENTS: Data from a prospective, observational cohort study (HIV-Longitudinal Interrelationships of Viruses and Ethanol) were used to assess the association between awareness of having HCV at baseline and subsequent abstinence and not drinking unhealthy amounts as reported at 6-month follow-up intervals. General estimating equations logistic regression was used to account for the correlation from using repeated observations from the same subject over time. We adjusted for age, sex, race, homelessness, injection drug use, depressive symptoms, and having abnormal liver tests. RESULTS: Participants who reported being told they had HCV were more likely to report abstaining from alcohol (AOR = 1.60; 95% CI: 1.13 to 2.27) and not drinking unhealthy amounts (AOR = 1.46; 95% CI: 1.01 to 2.11). CONCLUSIONS: Among patients infected with HIV who had a history of alcohol problems, reporting being told one had HCV was associated with greater abstinence from alcohol and less unhealthy amounts of drinking.


Subject(s)
Alcohol Drinking/psychology , Alcoholism/psychology , HIV Infections/psychology , Health Behavior , Hepatitis C/psychology , Adult , Alcoholism/complications , Awareness , Female , HIV Infections/complications , Hepatitis C/complications , Hepatitis C/diagnosis , Humans , Male , Middle Aged , Prospective Studies
4.
Alcohol Clin Exp Res ; 31(5): 829-36, 2007 May.
Article in English | MEDLINE | ID: mdl-17403066

ABSTRACT

BACKGROUND: Coinfection of human immunodeficiency virus (HIV) and hepatitis C virus (HCV) is a substantial medical and public health concern due to its increasing prevalence and complex patient management. Alcohol use may worsen HCV-related liver disease and interfere with adherence to antiretroviral therapy (ART) and medical care. We therefore studied the association between HCV infection and markers of HIV disease progression in adults with alcohol problems. METHODS: This is a longitudinal study of 396 HIV-infected persons with alcohol problems, 199 (50%) of whom were coinfected with HCV (positive HCV RNA test). CD4 cell counts and HIV RNA levels were assessed at baseline and then every 6 months for up to 42 months. Hepatitis C virus RNA status was determined at study enrollment. We examined the relationship between HCV infection and laboratory markers of HIV progression (CD4 cell count and log10 HIV RNA) by fitting multivariable longitudinal regression models for each outcome. RESULTS: Among subjects who were adherent to ART, the presence of HCV infection was associated with a lower CD4 cell count (adjusted mean difference -46.0 cells/microL, p=0.03). There was no association observed between HCV infection and CD4 cell count among those not adherent to ART or those not taking ART. No significant association was observed between HCV infection and HIV RNA regardless of ART status. CONCLUSIONS: Hepatitis C virus infection has an adverse effect on CD4 cell count in patients with alcohol problems who are adherent to ART. Addressing HCV coinfection among these patients may confer additional immunologic benefit for this patient population.


Subject(s)
Alcoholism/complications , HIV Infections/complications , HIV Infections/pathology , Hepatitis C/complications , Hepatitis C/pathology , Adult , Alcohol Drinking/psychology , Antiretroviral Therapy, Highly Active , CD4 Lymphocyte Count , Disease Progression , Enzyme-Linked Immunosorbent Assay , Female , Humans , Longitudinal Studies , Male , Models, Statistical , Patient Compliance , RNA, Viral/blood , Regression Analysis , Risk-Taking , Sample Size , Treatment Outcome
5.
Am J Gastroenterol ; 101(8): 1804-10, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16780562

ABSTRACT

OBJECTIVES: Depression is common in persons with HIV infection and with alcohol problems, and it has important prognostic implications. Neurocognitive dysfunction has been reported with chronic hepatitis C virus (HCV) infection. We hypothesized that HCV infection is associated with more depressive symptoms in HIV-infected persons with a history of alcohol problems. METHODS: We performed a cross-sectional analysis of baseline data from a prospective cohort study of 391 HIV-infected subjects with a history of alcohol problems, of whom 59% were HCV antibody (Ab) positive and 49% were HCV RNA-positive. We assessed depressive symptoms (Center for Epidemiologic Studies Depression [CES-D]) and past month alcohol consumption. In the primary analysis, we evaluated whether there were more depressive symptoms in HCV Ab-positive and RNA-positive subjects in unadjusted analyses and adjusting for alcohol consumption, gender, age, race, CD4 count, homelessness, drug dependence, and medical comorbidity. RESULTS: Mean CES-D scores were higher in subjects who were HCV Ab-positive compared with those who were HCV Ab-negative (24.3 vs 19.0; p < 0.001). In adjusted analyses, the difference in CES-D scores between HCV Ab-positive and Ab-negative subjects persisted (24.0 vs 19.0; p < 0.001). Unadjusted mean CES-D scores were also significantly higher in HCV RNA-positive subjects compared with those who were RNA-negative, and the difference remained significant (24.6 vs 19.3; p < 0.001) in adjusted analyses. CONCLUSIONS: HCV/HIV coinfected persons with a history of alcohol problems have more depressive symptoms than those without HCV, and this association is unexplained by a variety of population characteristics. These data suggest that HCV may have a direct effect on neuropsychiatric function.


Subject(s)
Alcoholism/psychology , Depression/psychology , HIV Infections/psychology , Hepatitis C, Chronic/psychology , Adult , Age Factors , Alcoholism/complications , Blotting, Western , CD4 Lymphocyte Count , Chi-Square Distribution , Comorbidity , Cross-Sectional Studies , Depression/complications , Depression/epidemiology , Enzyme-Linked Immunosorbent Assay , Female , HIV Infections/complications , Hepatitis C, Chronic/complications , Ill-Housed Persons , Humans , Linear Models , Male , Massachusetts/epidemiology , Middle Aged , Prognosis , Risk Assessment , Sex Factors
6.
Am J Public Health ; 93(3): 477-81, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12604499

ABSTRACT

OBJECTIVES: This study explored whether work or immigration concerns affect women's participation in the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC). METHODS: The sample included women who had withdrawn from the WIC program and current WIC clients from 1 center in New York City. Logistic regression analyses were used to predict noncollection of checks; demographic characteristics, program participation, and problems with the WIC program were independent variables. RESULTS: Strong predictors of noncollection of checks were job conflicts, transportation or illness problems, and WIC receipt by the woman herself (rather than by her children). CONCLUSIONS: Employment conflicts were related to failure to pick up WIC checks; immigration concerns were not. As a means of enhancing WIC participation, flexibility is recommended in terms of center hours, locations, and staffing and program check distribution policies.


Subject(s)
Aid to Families with Dependent Children/statistics & numerical data , Child Health Services/economics , Community Participation/statistics & numerical data , Maternal Health Services/economics , Women/psychology , Adult , Child, Preschool , Employment , Female , Health , Health Care Surveys , Humans , Infant , Infant, Newborn , Logistic Models , Medicaid/statistics & numerical data , New York City , Transportation
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