Document Detail

Predictors of latent tuberculosis treatment initiation and completion at a U.S. public health clinic: a prospective cohort study.
Jump to Full Text
MedLine Citation:
PMID:  22720842     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: Treatment of latent tuberculosis infection (LTBI) is a key component in U.S. tuberculosis control, assisted by recent improvements in LTBI diagnostics and therapeutic regimens. Effectiveness of LTBI therapy, however, is limited by patients' willingness to both initiate and complete treatment. We aimed to evaluate the demographic, medical, behavioral, attitude-based, and geographic factors associated with LTBI treatment initiation and completion of persons presenting with LTBI to a public health tuberculosis clinic.
METHODS: Data for this prospective cohort study were collected from structured patient interviews, self-administered questionnaires, clinic intake forms, and U.S. census data. All adults (>17 years) who met CDC guidelines for LTBI treatment between January 11, 2008 and May 6, 2009 at Wake County Health and Human Services Tuberculosis Clinic in Raleigh, North Carolina were included in the study. In addition to traditional social and behavioral factors, a three-level medical risk variable (low, moderate, high), based on risk factors for both progression to and transmission of active tuberculosis, was included for analysis. Clinic distance and neighborhood poverty level, based on percent residents living below poverty level in a person's zip code, were also analyzed. Variables with a significance level <0.10 by univariate analysis were included in log binomial models with backward elimination. Models were used to estimate risk ratios for two primary outcomes: (1) LTBI therapy initiation (picking up one month's medication) and (2) therapy completion (picking up nine months INH therapy or four months rifampin monthly).
RESULTS: 496 persons completed medical interviews and questionnaires addressing social factors and attitudes toward LTBI treatment. 26% persons initiated LTBI therapy and 53% of those initiating completed therapy. Treatment initiation predictors included: a non-employment reason for screening (RR 1.6, 95% CI 1.0-2.5), close contact to an infectious TB case (RR 2.5, 95% CI 1.8-3.6), regular primary care(RR 1.4, 95% CI 1.0-2.0), and history of incarceration (RR 1.7, 95% CI 1.0-2.8). Persons in the "high" risk category for progression/transmission of TB disease had higher likelihood of treatment initiation (p < 0.01), but not completion, than those with lower risk.
CONCLUSIONS: Investment in social support and access to regular primary care may lead to increased LTBI therapy adherence in high-risk populations.
Authors:
Neela D Goswami; Lara Beth Gadkowski; Carla Piedrahita; Deborah Bissette; Marshall Alex Ahearn; Michela L M Blain; Truls Østbye; Jussi Saukkonen; Jason E Stout
Publication Detail:
Type:  Journal Article     Date:  2012-06-21
Journal Detail:
Title:  BMC public health     Volume:  12     ISSN:  1471-2458     ISO Abbreviation:  BMC Public Health     Publication Date:  2012  
Date Detail:
Created Date:  2012-09-11     Completed Date:  2012-12-21     Revised Date:  2013-07-12    
Medline Journal Info:
Nlm Unique ID:  100968562     Medline TA:  BMC Public Health     Country:  England    
Other Details:
Languages:  eng     Pagination:  468     Citation Subset:  IM    
Affiliation:
Duke University Medical Center, Durham, NC, USA. neela.goswami@duke.edu
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adult
Aged
Aged, 80 and over
Female
Humans
Latent Tuberculosis / therapy*
Male
Middle Aged
Patient Acceptance of Health Care / statistics & numerical data*
Prospective Studies
Qualitative Research
Questionnaires
Risk Factors
Socioeconomic Factors
United States
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Full Text
Journal Information
Journal ID (nlm-ta): BMC Public Health
Journal ID (iso-abbrev): BMC Public Health
ISSN: 1471-2458
Publisher: BioMed Central
Article Information
Download PDF
Copyright ©2012 Goswami et al.; licensee BioMed Central Ltd.
open-access:
Received Day: 13 Month: 1 Year: 2012
Accepted Day: 21 Month: 6 Year: 2012
collection publication date: Year: 2012
Electronic publication date: Day: 21 Month: 6 Year: 2012
Volume: 12First Page: 468 Last Page: 468
ID: 3438075
Publisher Id: 1471-2458-12-468
PubMed Id: 22720842
DOI: 10.1186/1471-2458-12-468

Predictors of latent tuberculosis treatment initiation and completion at a U.S. public health clinic: a prospective cohort study
Neela D Goswami1 Email: neela.goswami@duke.edu
Lara Beth Gadkowski1 Email: beth.gadkowski@gmail.com
Carla Piedrahita2 Email: Carla.piedrahita@wakegov.com
Deborah Bissette2 Email: Deborah.bissett@wakegov.com
Marshall Alex Ahearn3 Email: marshall.ahearn@gmail.com
Michela LM Blain3 Email: michela.blain@gmail.com
Truls Østbye3 Email: ostby001@mc.duke.edu
Jussi Saukkonen4 Email: jsaukk@bu.edu
Jason E Stout1 Email: stout002@mc.duke.edu
1Duke University Medical Center, Durham, NC, USA
2Wake County Human Services, Raleigh, NC, USA
3Duke University, Durham, NC, USA
4Boston University School of Medicine, Boston, MA, USA

Background

Latent tuberculosis infection (LTBI) treatment is a key strategy to reduce TB disease incidence in industrialized countries. Despite recent advances in LTBI diagnostics and up to 90 percent efficacy of first-line therapy for LTBI if taken properly, the proportion of patients who complete prescribed therapy remains low, ranging from 50-65% [1-3]. Firstly, LTBI therapy initiation requires patient motivation and understanding of the diagnosis, adequate communication between health department staff and the patient, and availability of transportation to pick up initial medications; barriers can arise to any of these components. Therapy completion is a second, independent step with potentially different and additional barriers at each visit, such as increased fear of medication side effects, logistical issues, or negative attitudes towards treatment that emerge over time.

Suboptimal compliance with traditional TB preventative therapy has been attributed to various factors, including duration of therapy, concerns about drug toxicity, and pill burden [4]. Studies comparing four months of rifampin or two months of rifampin and pyrazinamide to the traditional nine months of isoniazid (INH) note improved adherence to the shorter regimens [5-7], but increased hepatotoxicity with rifampin-pyrazinamide led to withdrawal of the regimen from CDC recommendations [8]. Studies evaluating three months of rifampin plus INH versus six months of INH, have noted no significant difference in completion rates, possibly secondary to the increased pill burden of a two-drug regimen [9]. A study of three months directly-observed therapy with rifapentine and INH versus self-administered nine months INH was also recently completed, with adherence data forthcoming [10].

Aside from factors relating to therapy, other predictors of medication adherence have been less prospectively studied. Factors that have been consistently associated with treatment completion in retrospective studies include non-U.S. birthplace [11-13] and recent exposure to an active tuberculosis case [4,14]. Age and other demographics have been less consistently associated with treatment adherence across studies, with some suggesting older age and others suggesting younger age correlating with therapy adherence [11,13-16]. Certain patient attitudes and social factors have also been correlated with LTBI therapy non-completion, including perception of a low risk of progression to active TB without LTBI treatment, dislike of venipuncture [16], fear about side effects [11,15], lower educational level [4,17], and unstable housing [4,11].

As identifying LTBI, initiating therapy, and adherence to LTBI therapy serve as the cornerstones of U.S. TB control efforts, prospective studies evaluating predictive factors in treatment completion will not only help modernize and improve treatment strategies, but also allow more educated and tailored interventions in cases of noncompliance. The aim of this study was to understand barriers to LTBI treatment initiation and completion by determining demographic, medical, behavioral, attitude-based, and geographic factors potentially associated with therapy adherence in LTBI-infected patients recommended for treatment by the Wake County TB clinic in Raleigh, North Carolina. Based on anecdotal experience in the clinic, we hypothesized that those persons at highest risk of progressing to active TB disease and spreading TB infection to others, as well as those living in poorer geographical areas, would be less likely to initiate and complete therapy.


Methods
Study setting and patient recruitment

All adults (>17 years) who met CDC guidelines for LTBI treatment between January 11, 2008 and May 6, 2009 at Wake County Tuberculosis Clinic in Raleigh, North Carolina were included in the study. Written informed consent was waived by the Duke Institutional Review Board, as this was considered an evaluation of a public benefit program, and thus eligible for such a waiver under the United States Code of Federal Regulations part 45 46.116(c)(1). The study was also approved by the Wake County Human Rights-Consumer Affairs and Human Research Committee.

Data collection

On entry to the TB clinic, a routine medical interview was conducted, followed by a self-administered multiple choice questionnaire addressing social factors and attitudes toward LTBI treatment (Table 1). The questionnaire was developed based on the results of a focus group study assessing TB-related knowledge, attitudes, and behaviors among key populations in the region [18]. The questionnaire was validated by administering it to a pilot population of individuals taking isoniazid therapy at baseline and one month later; in this group test-retest response concordance was >0.75.

Provision of treatment

All LTBI medications were provided free of charge by the health department from an on-site pharmacy, which recorded all medication pickups in a computerized system.

Statistical methods

Primary endpoints were 1) LTBI therapy initiation, defined as picking up at least one month of medication, and 2) therapy completion, defined as picking up nine months of INH therapy within a 12-month period or four months of rifampin within a six-month period. Univariate analysis was performed with survey responses, demographics, and medical risk data, using chi square test or Fischer’s exact test for categorical variables as appropriate. For multi-level categorical variables, pairwise testing was performed with chi square Univariate analysis was also performed to examine the relationship between the risk that an individual would transmit TB in the future and the likelihood of a) initiating and b) completing LTBI treatment. Subjects were placed in three risk categories, which were based on a combination of medical risk (risk of progression to active TB) and social risk (transmission risk due to suboptimal healthcare utilization). Subjects with history of transplant, HIV, silicosis, intravenous drug use, close contact to an infectious TB case, or with evidence of old tuberculosis on chest radiograph were placed in the “High risk” category. Persons with diabetes, end-stage renal disease, history of gastrectomy, homelessness, or being underweight were placed in the “Moderate risk” category, and all others were considered “Low risk.” Backward elimination was used to arrive at a final log binomial model consisting of independent variables significantly associated with completion of LTBI therapy at p < 0.10 by univariate analysis plus any significant confounders. Significant confounding was defined as a change in the risk ratio for a second variable of interest of >10% when the confounder was included (vs. not included) in the model.

Geospatial analysis

Residences of study participants were geocoded and mapped using ArcMap 9.3 GIS software. The point density analyst tool was used to calculate distances between each residence address and the Wake County Health Department. Mean distance from the health department was compared between those who initiated and completed therapy and those who did not, using the student’s t-test. Residence zip codes were linked to percentage of area residents living below the poverty line in each zip code, based on Census 2000 data. Zip codes with less than 5% of the population living below the poverty line were categorized as “Low poverty,” those with 5-10% below the poverty line “Moderate poverty” and those with greater than 10% below the poverty line “High poverty.” Univariate relationships between these three categories and LTBI therapy initiation and completion were assessed.


Results
Patient characteristics

The 496 participants were predominantly foreign-born (65%) and racial/ethnic minorities (87%), with mean age 39.1 + 12.3 years (Table 2). Of the 496, 130 (26%) persons initiated LTBI therapy and 70 (54% of those initiating) completed therapy. Of those who were foreign-born, the most frequent regions of origin were Africa (19%) and Latin America (20%). 61% of persons included in the study were referred after a tuberculin skin test (TST) was performed as part of employment screening, and 19% received a TST as part of a contact investigation. The overall cohort included a number of former or current smokers (32%), drug users (9%), and persons with history of incarceration (14%) or homelessness (11%).

LTBI treatment initiation

In the univariate analysis, factors significantly associated with treatment initiation (P < 0.10) included older age, African birthplace, close contact with an infectious TB case, non-employment reason for TST, end-stage renal disease (ESRD), immunosuppressed status, HIV infection, previous incarceration, residence in current home for greater than one year, plans to remain at same home greater than one year, lower educational level, having a regular physician, and fear of getting sick with tuberculosis (Tables 1 and 2). In multivariable analysis, close contact with a TB case, non-employment reason for screening, lower educational level, having a regular physician, fear of getting sick with TB, and prior incarceration were independently associated with treatment initiation (Table 3). Since there were few (n < 20) persons with specific medical risk factors (ESRD, immunosuppressed status, HIV), medical and social risk were collapsed into three risk strata as described in the Methods section. More persons at “high risk” of progressing to and/or transmitting active TB initiated LTBI therapy (54/120, 45%) than those at “moderate risk” (24/69, 35%) or “low risk” (52/307, 17%)(P < 0.01).

LTBI treatment completion

Among those initiating treatment, factors associated with treatment completion (P < 0.10) included African or Asian birthplace, absence of tobacco history, prior incarceration, and plan to tell friends/family about positive TST. In multivariable analysis, planning to tell friends/family about positive TST was independently and significantly associated with treatment completion (RR 2.0, 95% CI 1.0-3.9). The proportion of persons at high risk of progressing to and/or transmitting active TB completing therapy was not significantly different from those at moderate or low risk (p = 0.6).

Of those persons initiating therapy, 31 were prescribed rifampin, with a 61% completion rate, and 99 persons were prescribed INH, with a 52% nine-month completion rate (p = 0.3). At least six months of INH was completed by 62/99 (63%) persons. Seven persons were switched from isoniazid to rifampin, and four of these completed a full course of rifampin. One person was switched from rifampin to isoniazid and that individual completed a full course of isoniazid. Compliance with both therapies declined over time (Figure 1).

Geospatial analysis

In geographic analysis, 391 residential addresses were mapped with ArcGIS software. Of the 130 who initiated therapy, 99 participants had addresses that could be mapped to a physical location in North Carolina. Distance from the health department was not significantly different between addresses of persons who initiated LTBI therapy and those who did not initiate therapy (p = 0.4). Similarly, treatment completion was not significantly associated with distance from the health department (p = 0.9). Of all participants, 378 participants had zip codes with poverty data available from the 2000 U.S. census. Treatment initiation did not vary significantly by whether a participant lived in a high, moderate, or low-poverty level area (p = 0.6). Of those who initiated therapy, there was a trend toward greater completion of therapy by persons living in a low-poverty area (81% of those initiating completed therapy), compared to those living in a moderate (49% completed) or high poverty area (42%), at p = 0.08.


Discussion

Previous authors have evaluated demographic and medication-based predictors of LTBI treatment non-completion, but few, if any, have prospectively evaluated a combination of pre-treatment attitudes, behaviors, geographic, and medical risk factors as they relate to both initiating and completing therapy.

Furthermore, while several studies have evaluated medication completion in a cohort of patients already initiated on therapy [2,4,14,16], one of the most interesting observations in our study was the fact that initiating, rather than completing, treatment was the major challenge in the LTBI program. While about half (55%) of persons initiating therapy completed, only about a quarter (26%) even initiated therapy by picking up the first month’s supply of pills. The initiation rate in our study is notably less than the 91% LTBI therapy initiation rate seen in a cohort of patients presenting to TB clinic at Boston Medical Center [12], 58% initiation rate in a population of health care workers in Toronto [19], and 67% initiation rate in a cohort of HIV-infected patients in Spain [20]. Differences in initiation rates between our study and others may be attributable to different clinic populations, healthcare systems, and the fact that our study, as a program evaluation, included all persons prescribed LTBI treatment without selection bias. For comparison, among all contact investigations conducted in the U.S. in 2006, 72% of those infected with latent TB started treatment [21]. Among contacts in North Carolina in 2009, 67% of those infected started treatment (Kitty Herrin, PhD, personal communication), consistent with our data that close contacts to an infectious TB case are 2.5 times as likely to start therapy than non-contacts.

This study also demonstrated that those with prior incarceration were also more likely to initiate therapy, likely because LTBI treatment was started in a jail or prison setting, although this data was not specifically documented. Routine access to medical care with a regular physician also increased likelihood of therapy initiation, suggesting that continuity of primary care can improve TB control efforts.

Contrary to our hypothesis, persons we classified as higher risk of progression to active TB were more likely to initiate LTBI treatment than persons at lower risk. Unfortunately, even in these high-risk groups, though, a relatively low proportion of participants with LTBI initiated treatment. The likelihood that LTBI treatment would be completed once initiated had no relationship to risk group. Completion was associated with the plan to disclose LTBI diagnosis with friends or family, suggesting that invitation of support members to clinic visits or to otherwise engage in a patient’s care may improve completion rates. Other novel and cost-efficient interventions need to be studied to improve both initiation and completion of LTBI treatment. In a California study of LTBI treatment in drug users, therapy completion rate was 53% when active outreach was used with a financial incentive of five dollars per visit, compared to 4% when active outreach was used alone (p < 0.0001) [22]. A nonmonetary incentive such as a nutritional supplement has also been associated with increased LTBI therapy completion [23]. Directly observed therapy has had less success in increasing treatment completion [24], and educational interventions have had variable impact on adherence.

The impact of a case of active TB may differ based upon where the case occurs. A case in a relatively high-poverty area, further from the health department, may take longer to detect because of financial and logistical barriers to seeking TB-related healthcare [15,17]. While distance from the health department and the economic status of the patient’s neighborhood were not related to the probability of initiating LTBI treatment, of those who initiated therapy, there was a trend toward greater completion of therapy by persons living in low-poverty areas than persons living in higher poverty areas. The higher completion in lower-poverty areas may be due to ease of access to healthcare, local social factors, or other unmeasured factors. Also, while distance to the health department from a participant’s residential address was not significantly related to the probability of initiating or completing LTBI treatment, the distance measures used in our study are only rough approximations of the time required to get to the health department.

In terms of study limitations, results may be less generalizable given this was a single-clinic cohort. Furthermore, employment screening, a less targeted approach, was a frequent reason for TST placement and medication prescription in this clinic; this type of screening was discontinued in part as a result of this analysis. Finally, the small number of participants with key risk factors for LTBI (HIV, immunosuppressed conditions, etc.) and overall small numbers in the completion group limited the power of multivariable analysis.


Conclusion

Initiation of treatment was the major challenge in our program. Investment in non-employment based screening, social support, and in treatment completion by persons at high risk of developing TB, may improve control efforts in low-incidence settings.


Competing interests

The authors declare that they have no competing interests.


Authors’ contributions

JES, LBG, and NDG conceived of the study, and participated in study design and coordination. CP, DB, MAA, and MLMB participated in study design and coordination. NDG and JES performed statistical analysis and drafted the manuscript. TO and JS helped with data analysis and drafting of the manuscript. All authors read and approved the final manuscript.


Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2458/12/468/prepub


Acknowledgements

We would like to acknowledge the tuberculosis nurses at the Wake County Health Department who facilitated implementation of the study and collection of data.


References
Jasmer RM,Saukkonen JJ,Blumberg HM,Daley CL,Bernardo J,Vittinghoff E,King MD,Kawamura LM,Hopewell PC,Short-course rifampin and pyrazinamide compared with isoniazid for latent tuberculosis infection: a multicenter clinical trialAnn Intern MedYear: 2002137864064712379063
Trajman A,Long R,Zylberberg D,Dion MJ,Al-Otaibi B,Menzies D,Factors associated with treatment adherence in a randomised trial of latent tuberculosis infection treatmentInt J Tuberc Lung DisYear: 201014555155920392347
Horsburgh CR,Goldberg S,Bethel J,Chen S,Colson PW,Hirsch-Moverman Y,Hughes S,Shrestha-Kuwahara R,Sterling TR,Wall K,et al. Latent TB infection treatment acceptance and completion in the United States and CanadaChestYear: 2010137240140910.1378/chest.09-039419793865
Hirsch-Moverman Y,Daftary A,Franks J,Colson PW,Adherence to treatment for latent tuberculosis infection: systematic review of studies in the US and CanadaInt J Tuberc Lung DisYear: 200812111235125418926033
Ziakas PD,Mylonakis E,4 months of rifampin compared with 9 months of isoniazid for the management of latent tuberculosis infection: a meta-analysis and cost-effectiveness study that focuses on compliance and liver toxicityClin Infect DisYear: 200949121883188910.1086/64794419911936
Gordin F,Chaisson RE,Matts JP,Miller C,de Lourdes Garcia M,Hafner R,Valdespino JL,Coberly J,Schechter M,Klukowicz AJ,et al. Rifampin and pyrazinamide vs isoniazid for prevention of tuberculosis in HIV-infected persons: an international randomized trial. Terry Beirn Community Programs for Clinical Research on AIDS, the Adult AIDS Clinical Trials Group, the Pan American Health Organization, and the Centers for Disease Control and Prevention Study GroupJAMAYear: 2000283111445145010.1001/jama.283.11.144510732934
Halsey NA,Coberly JS,Desormeaux J,Losikoff P,Atkinson J,Moulton LH,Contave M,Johnson M,Davis H,Geiter L,et al. Randomised trial of isoniazid versus rifampicin and pyrazinamide for prevention of tuberculosis in HIV-1 infectionLancetYear: 1998351910578679210.1016/S0140-6736(97)06532-X9519950
CfDCaPCAT S,Update: adverse event data and revised American Thoracic Society/CDC recommendations against the use of rifampin and pyrazinamide for treatment of latent tuberculosis infection–United States, 2003MMWR Morb Mortal Wkly RepYear: 2003523173573912904741
Lobue P,Menzies D,Treatment of latent tuberculosis infection: an updateRespirologyYear: 201015460362210.1111/j.1440-1843.2010.01751.x20409026
Sterling TR BA,Shang N,Bliven-Sizemore E,Chaisson RE,Gordin F,Hackman J,Hamilton CD,Horsburgh CR,Kerrigan A,Menzies D,Scott N,Villarino ME,and the Tuberculosis Trials ConsortiumThe PREVENT TB Study of 3 months of once-weekly rifapentine plus INH vs. 9 months of daily INH for treatment of latent TB infection: first report of results of a multi-center, randomized clinical trialYear: 2010In: 41st Union World Conference on Lung Health: November 2010, Berlin, Germany
LoBue PA,Moser KS,Use of isoniazid for latent tuberculosis infection in a public health clinicAm J Respir Crit Care MedYear: 2003168444344710.1164/rccm.200303-390OC12746255
Parsyan AE,Saukkonen J,Barry MA,Sharnprapai S,Horsburgh CR,Predictors of failure to complete treatment for latent tuberculosis infectionJ InfectYear: 200754326226610.1016/j.jinf.2006.04.01016772095
Shukla SJ,Warren DK,Woeltje KF,Gruber CA,Fraser VJ,Factors associated with the treatment of latent tuberculosis infection among health-care workers at a midwestern teaching hospitalChestYear: 200212251609161410.1378/chest.122.5.160912426260
Li J,Munsiff SS,Tarantino T,Dorsinville M,Adherence to treatment of latent tuberculosis infection in a clinical population in New York CityInt J Infect DisYear: 2010144e292e29710.1016/j.ijid.2009.05.00719656705
Machado A,Finkmoore B,Emodi K,Takenami I,Barbosa T,Tavares M,Reis MG,Arruda S,Riley LW,Risk factors for failure to complete a course of latent tuberculosis infection treatment in Salvador, BrazilInt J Tuberc Lung DisYear: 200913671972519460247
Shieh FK,Snyder G,Horsburgh CR,Bernardo J,Murphy C,Saukkonen JJ,Predicting non-completion of treatment for latent tuberculous infection: a prospective surveyAm J Respir Crit Care MedYear: 2006174671772110.1164/rccm.200510-1667OC16809632
Zuniga JA,Medication adherence in hispanics to latent tuberculosis treatment: a literature reviewJ Immigr Minor HealthYear: 201014123920872072
West EL,Gadkowski LB,Ostbye T,Piedrahita C,Stout JE,Tuberculosis knowledge, attitudes, and beliefs among North Carolinians at increased risk of infectionN C Med JYear: 2008691142018429559
Gershon AS,McGeer A,Bayoumi AM,Raboud J,Yang J,Health care workers and the initiation of treatment for latent tuberculosis infectionClin Infect DisYear: 200439566767210.1086/42299515356781
Diaz A,Diez M,Bleda MJ,Aldamiz M,Camafort M,Camino X,Cepeda C,Costa A,Ferrero O,Geijo P,et al. Eligibility for and outcome of treatment of latent tuberculosis infection in a cohort of HIV-infected people in SpainBMC Infect DisYear: 20101026710.1186/1471-2334-10-26720840743
Akhtar N,Khan BA,Mahmood T,Parveen R,Qayum M,Anwar M,Shahiq Uz Z,Farooq M,Formulation and evaluation of antisebum secretion effects of sea buckthorn w/o emulsionJ Pharm Bioallied SciYear: 201021131710.4103/0975-7406.6269821814424
Malotte CK,Hollingshead JR,Larro M,Incentives vs outreach workers for latent tuberculosis treatment in drug usersAm J Prev MedYear: 200120210310710.1016/S0749-3797(00)00283-X11165450
Mangura BT,Passannante MR,Reichman LB,An incentive in tuberculosis preventive therapy for an inner city populationInt J Tuberc Lung DisYear: 1997165765789487458
Volmink J,Garner P,Directly observed therapy for treating tuberculosisCochrane Database Syst RevYear: 20074CD00334317943789

Figures

[Figure ID: F1]
Figure 1 

Adherence to latent tuberculosis infection by therapy, Wake County 2008–2009. In this study, of persons initiating therapy, 31 were prescribed rifampin, with a 61% completion rate, and 99 persons were prescribed INH, with a 52% nine-month completion rate (p = 0.3). At least six months of INH was completed by 62/99 (63%) persons. Compliance with both therapies declined over time.



Tables
[TableWrap ID: T1] Table 1 

Latent TB infection therapy initiation and completion based on responses to survey questions


Variable Treatment Initiation (%) P-value Treatment Completion (%) P-value*
Length of time at current residence
 Less than 1 yr
20
0.01
52
0.8
 Greater or equal to 1 year
31
 
55
 
Planned future time at current residence
 Less than 1 yr
19
0.04
46
0.3
 Greater or equal to 1 year
28
 
58
 
 No school
50
0.01
0
0.5
 Elementary school
41
 
61
 
 High school/GED
30
 
49
 
 College
18
 
64
 
 Graduate school
23
 
53
 
Cohabitance with any family members
 Yes
27
0.6
57
0.3
 No
24
 
47
 
Previous daily pill for at least 6 months
 Yes
29
0.2
49
0.3
 No
24
 
59
 
Regular primary care
 
 
 
 
 Yes
37
<0.01
52
0.5
 No
19
 
59
 
Easy access to health department
 Yes
28
0.1
54
0.8
 No
19
 
57
 
Plan to tell family/friends about positive skin test
 Yes
25
 
59
 
 No
35
0.1
30
0.02
Belief in getting sick from TB without medicine
 Yes
34
<0.01
53
0.6
 No
15
 
58
 
Fear of adverse effects from medicine
 Yes
24
0.3
55
0.8
 No
28
 
52
 
Belief in medicine efficacy
 Yes
28
0.3
55
0.6
 No
21
 
46
 
Belief in cure for TB
 
 
 
 
 Yes
26
0.9
55
0.7
 No
27
 
60
 
Fear of phlebotomy
 Yes
25
0.8
50
0.7
 No 26   56  

*P-values represent differences in initiation/completion among responses (missing responses not included).


[TableWrap ID: T2] Table 2 

Demographics, Risk Factors and Behaviors among Study Population with Latent TB Infection


Variable
N (%) or
N (%) or
P value
N (%) or
P value
 
Mean (SD)
Mean (SD)
 
Mean (SD)
 
  Total Population Who Initiated Therapy   Who Completed Therapy  
Race/ethnicity
 
 
 
 
 
 Asian/Pacific
 
 
 
 
 
 Islander
70 (14)
16 (23)
0.2
12 (75)
0.1
 Non-Hispanic White
64 (13)
10 (16)
 
3 (30)
 
 Non-Hispanic Black
254 (51)
67 (26)
 
39 (58)
 
 Hispanic
92 (19)
28 (30)
 
12 (43)
 
 Other/unknown
16 (3)
 
 
 
 
Gender
 
 
 
 
 
 Male
236 (48)
67 (28)
0.3
39 (58)
0.3
 Female
260 (52)
63 (24)
 
31 (49)
 
Mean age
39.1 (12.3)
42.1 (38.0)
<0.01
42.8 (41.2)
0.5
US-born
169 (34)
57 (34)
0.01
26 (46)
0.07
Region of birth
 
 
 
 
 
 Developed world (US, Canada,
 
 
 
 
 
 Western Europe, Japan)*
175 (35)
57 (33)
0.01
26 (46)
0.03
 Africa
94 (19)
17 (18)
0.23
13 (77)
0.04
 Asia
65 (13)
16 (25)
0.07
12 (75)
1
 Eastern Europe
13 (3)
1 (8)
0.87
0 (0)
0.8
 Latin America
98 (20)
31 (32)
0.06
15 (48)
1
 Middle East
19 (4)
2 (11)
0.12
1 (50)
1
 Other/unknown
32 (7)
6 (19)
 
3 (50)
 
Reason for skin testing
 
 
 
 
 
 Employment screening *
304 (61)
50 (17)
<0.01
25 (50)
0.3
 Contact to TB case
94 (19)
50 (53)
<0.01
30 (60)
1
 Non-employment reason
98 (20)
30 (31)
 
15 (50)
 
Mean distance from health department (miles)
 
7.9 (9.5)
0.4
8.0 (7.7)
0.9
Neighborhood poverty level
 
 
 
 
 
 Low poverty
74 (20)
16 (22)
0.6
13 (81)
0.08
 Moderate poverty
155 (41)
39 (25)
 
19 (49)
 
 High poverty
149 (39)
42 (28)
 
22 (42)
 
Alcohol use
 
 
 
 
 
 None
316 (64)
82 (26)
0.7
41 (50)
0.3
 <1 drink/day
106 (21)
31 (29)
 
22 (71)
 
 1-2 drinks/day
23 (5)
5 (22)
 
2 (40)
 
 3+ drinks/day
23 (5)
4 (17)
 
2 (50)
 
 Binge
15 (3)
5 (33)
 
2 (40)
 
Smoking
 
 
 
 
 
 None
322 (65)
84 (26)
0.7
51 (61)
0.04
 Former
59 (12)
18 (31)
 
10 (56)
 
 Current
100 (20)
25 (25)
 
8 (32)
 
Crack cocaine use
34 (7)
12 (35)
0.2
4 (33)
0.2
Diabetes
28 (6)
11 (39)
0.1
7 (64)
0.5
ESRD
3 (1)
3 (100)
0.02
1 (33)
0.6
Gastrectomy
6 (1)
3 (50)
0.2
3 (100)
0.3
Heroin use
8 (2)
2 (25)
1
0 (0)
0.2
Homeless
53 (11)
18 (34)
0.2
8 (44)
0.4
IV drug use
12 (2)
3 (25)
1
0 (0)
0.1
Immunosuppressed
7 (1)
5 (71)
0.02
1 (20)
0.2
Prior incarceration
67 (14)
24 (36)
0.06
9 (38)
0.07
Long term care facility
71 (14)
12 (17)
0.05
8 (67)
0.4
Evidence of old TB on CXR
11 (2)
1 (9)
0.3
0 (0)
0.4
History of organ or bone marrow transplantation
1 (0)
0 (0)
1
0 (0)
1
Underweight
9 (2)
2 (22)
1
1 (50)
1
HIV 6 (1) 4 (67) 0.03 0 (0) 0.05

*Used as reference category for 2-group comparisons to calculate p-value.

P-values represent differences in proportions initiating/completing treatment among responses (not including missing responses).


[TableWrap ID: T3] Table 3 

Multivariable model (log binomial) predicting initiation and completion of treatment by backward elimination


Category Factor RR 95% CI
Treatment Initiation
Close contact to a TB case
2.5
1.8-3.6
 
Non-employment reason for screening
1.6
1.0-2.5
 
Lower educational level
1.3
1.1-1.6
 
Having a regular physician
1.4
1.0-2.0
 
Fear of getting sick with TB without medicine
1.7
1.2-2.6
 
Prior incarceration
1.7
1.1-2.8
Treatment Completion Plan to tell friends or family about LTBI diagnosis 2.0 1.0-3.9


Article Categories:
  • Research Article

Keywords: Adherence, LTBI, Compliance, Attitude, Geographic.

Previous Document:  Cerebrovascular responses to orthostatic stress after spinal cord injury.
Next Document:  Inhibitor of neuronal nitric oxide synthase improves gas exchange in ventilator-induced lung injury ...