Outcomes of a Tailored Intervention for Cigarette Smoking Cessation Among Latinos Living With HIV/AIDS

被引:37
|
作者
Stanton, Cassandra A. [1 ,2 ,3 ,4 ]
Papandonatos, George D. [5 ]
Shuter, Jonathan [6 ]
Bicki, Alexandra [1 ]
Lloyd-Richardson, Elizabeth E. [4 ,7 ]
de Dios, Marcel A. [8 ]
Morrow, Kathleen M. [4 ]
Makgoeng, Solomon B. [1 ]
Tashima, Karen T. [9 ]
Niaura, Raymond S. [2 ]
机构
[1] Georgetown Univ, Med Ctr, Canc Prevent & Control Program, Dept Oncol,Lombardi Comprehens Canc Ctr, Washington, DC 20057 USA
[2] Amer Legacy Fdn, Schroeder Inst Tobacco Res & Policy Studies, Washington, DC USA
[3] WESTAT Corp, Behav Hlth Grp, Rockville, MD 20850 USA
[4] Brown Univ, Warren Alpert Med Sch, Dept Psychiat & Human Behav, Providence, RI 02912 USA
[5] Brown Univ, Ctr Stat Sci, Providence, RI 02912 USA
[6] Albert Einstein Coll Med, Montefiore Med Ctr, Bronx, NY USA
[7] Univ Massachusetts, Dept Psychol, Amherst, MA 01003 USA
[8] MD Anderson Canc Ctr, Dept Hlth Dispar Res, Houston, TX USA
[9] Brown Univ, Miriam Hosp, Warren Alpert Med Sch, Dept Med, Providence, RI 02912 USA
基金
美国国家卫生研究院;
关键词
NICOTINE REPLACEMENT THERAPY; CANCER INFORMATION-SERVICE; MEXICAN-AMERICANS; FAGERSTROM TEST; SELF-EFFICACY; HEALTH-RISKS; HIV; SMOKERS; DEPENDENCE; TRIAL;
D O I
10.1093/ntr/ntv014
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Introduction: Tobacco use has emerged as a leading killer among persons living with HIV, with effective approaches to tobacco treatment still unknown. HIV infection is nearly 3 times as prevalent in Latinos than in non-Latino Whites. This study reports the results of a randomized trial comparing a tailored intervention to brief counseling for smoking cessation among Latino smokers living with HIV (LSLWH). Methods: LSLWH (N = 302; 36% female, 10% employed full-time, 49% born in United States) were randomized to 4 in-person sessions of a tailored intervention (Aurora) or 2 in-person sessions of brief advice (enhanced standard care [ESC]). Both groups received 8 weeks of nicotine replacement therapy (NRT) patch. Biochemically validated 6- and 12-month 7-day point-prevalence abstinence (PPA) rates were compared, along with secondary outcomes (e.g., reduction to light smoking, NRT adherence). Results: Seven-day PPA rates reached 8% versus 11% at 6 months and 6% versus 7% at 12 months, for Aurora and ESC, respectively, with no between-group differences (p values > .40). Significant changes from baseline to 6 and 12 months among intervention targets were noted (percentage reduction in heavy smoking and dependence; increases in knowledge and self-efficacy). Baseline smoking frequency, older age, and higher intensity of patch use during the trial emerged as significant predictors of abstinence at 6 months. Conclusions: There was no evidence that the tailored intervention improved cessation rates. Interventions that encourage use of, and adherence to, empirically validated cessation aids require further development to reduce tobacco-related death and disease in this vulnerable population.
引用
收藏
页码:975 / 982
页数:8
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