Bloss Et Al

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INT J TUBERC LUNG DIS 16(4):462–467

© 2012 The Union


http://dx.doi.org/10.5588/ijtld.11.0121

Increasing directly observed therapy related to improved


tuberculosis treatment outcomes in Taiwan

E. Bloss,* P-C. Chan,† N-W. Cheng,* K-F. Wang,† S-L. Yang,† P. Cegielski*
* US Centers for Disease Control and Prevention, Atlanta, Georgia, USA; † Taiwan Centers for Disease Control,
Taipei, Taiwan

SUMMARY

SETTING: Directly observed therapy (DOT) is a core el- an official DOT observer witnessed treatment was >60%
ement of tuberculosis (TB) care and control efforts. In for 5150 (45%) patients and ⩽60% for 4601 (40%) pa-
Taiwan, DOT was implemented in 2006, when the Stop tients, whereas for 1777 (15%) patients no days of DOT
TB Strategy was adopted as a national policy. were recorded. Being older, male, having positive bacte-
O B J E C T I V E : To quantify DOT among patients on anti- riology results and a non-World Health Organization
tuberculosis treatment and measure the association be- recommended treatment regimen at baseline were inde-
tween proportion of DOT and TB treatment outcomes pendently related to unsuccessful treatment outcomes
at a national level in Taiwan. and mortality. A dose-response effect was found between
D E S I G N : We analyzed data prospectively collected on all proportion of DOT and these outcomes.
new pulmonary TB cases reported to the national Web- C O N C L U S I O N : These findings highlight the importance
based registry between 1 January 2007 and 30 June 2008. of ensuring universal DOT in improving treatment out-
We compared treatment outcomes and proportion of comes among new pulmonary TB patients.
DOT in multivariable analyses. K E Y W O R D S : tuberculosis; directly observed therapy;
R E S U LT S : Among 11 528 patients initiating anti-tuber- treatment outcomes; Taiwan
culosis treatment, the proportion of days during which

TO ADDRESS the growing global burden of tuber- their medication regularly and complete treatment,
culosis (TB), a six-point Stop TB strategy was intro- thereby achieving cure and preventing drug resis-
duced in 2006,1,2 which includes high-quality DOTS tance. DOT has been associated with improved treat-
enhancement and expansion as one of its key ele- ment outcomes.9–11 However, other studies have
ments. Directly observed therapy (DOT) using stan- questioned the efficacy and necessity of DOT,12,13 or
dardized short-course chemotherapy is one of the have proposed a reduction in the frequency of obser-
recommended interventions to improve treatment vation.14 A meta-analysis by Volmink and Garner
adherence and help achieve the World Health Organi- found that DOT did not lead to better outcomes than
zation (WHO) recommended target of 85% treatment self-administered treatment in controlled trials.15 De-
success among new sputum smear-positive cases.1,3,4 spite these different conclusions, DOT is generally ac-
In 2007, 5.5 million TB cases were notified by cepted as an effective core element of TB care and
DOTS programs, and the target for treatment success control.9 However, many health care providers resist
rate was reached globally in 2006.5 However, due to implementing it. To help inform TB care and control
its duration, side effects and the need for frequent efforts in Taiwan, we sought to quantify DOT at the
clinic visits, anti-tuberculosis treatment continues to patient level and evaluate the association between
challenge health care providers worldwide.6 These proportion of DOT and treatment outcomes using
challenges often lead to non-adherence, compromis- prospectively collected data at a national level.
ing treatment effectiveness and leading to treatment
failure and mortality. METHODS
DOT can be defined as a trained person directly ob-
serving a patient swallowing anti-tuberculosis medi- Setting and patient population
cations to ensure the prescribed treatment is taken on In Taiwan, TB remains the most common notifiable
schedule.7,8 DOT is intended to help patients take infectious disease, with 14 265 cases reported and an

Correspondence to: Emily Bloss, Division of Tuberculosis Elimination, International Research and Programs Branch, CDC,
1600 Clifton Road, MS E-10, Atlanta, GA 30333, USA. Tel: (+1) 404 639 2658. Fax: (+1) 404 639 1566. e-mail: dpu2@
cdc.gov
Article submitted 18 February 2011. Final version accepted 19 October 2011.
DOT and treatment outcomes in Taiwan 463

estimated incidence of 62 per 100 000 population in cessful treatment outcomes included cure and treat-
2008.16 As part of the Stop TB strategy, the DOT pro- ment completion; unsuccessful outcomes included
gram was adopted in Taiwan in April 2006, and has failure, death and default.
been implemented in all 25 city and county health de-
partments. Within 1 year, approximately one third of Data analysis
TB patients received treatment via DOT in the public We restricted our analysis to all new pulmonary pa-
and private sectors.17 The proportion of cases com- tients who initiated anti-tuberculosis treatment and
pleting treatment nationally increased from 64% to were reported to the CDC Taiwan via the national
67% from 2005 to 2006, and in 2006 the treatment Web-based registry between 1 January 2007 and
success rate for DOT cases (75%) was higher than 30 June 2008. Patients previously treated for TB were
for non-DOT cases (52%).18 However, despite this excluded, as were patients with multidrug-resistant
positive trend, these findings do not control for other TB (MDR-TB), as they are known to have markedly
factors that may have influenced outcomes. different outcomes.21 We also excluded patients diag-
In Taiwan, once a TB case is verified, the patient is nosed with extra-pulmonary TB, as their treatment
invited to participate in the DOT program, and among regimen, duration and outcomes vary based on the
those who agree, an official DOT observer is assigned site of the disease.20 Cases were excluded if the pa-
to the patient.19 DOT observers are required to have tient was still on treatment or transferred out of the
9 years of education and DOT training, and are closely country, if the TB diagnosis was excluded after regis-
supervised by a public health nurse. Approximately tration, or if data for treatment days or outcomes
500 trained DOT observers are responsible for 5– were missing.
20 TB patients each, monitoring the ingestion of anti- Data were extracted from the national TB registry
tuberculosis medications during home visits or at a and managed and analyzed using SAS 9.2 (SAS Insti-
health facility at least five times per week, monitoring tute, Cary, NC, USA). The characteristics of patients
for adverse events and treatment complications, pro- receiving different proportions of DOT (>60%,
viding patients with food coupons as incentives and ⩽60% and no DOT) were compared using the χ2 test
entering their progress daily into an electronic Web- for categorical variables, and analysis of variance and
based national registry, the National Surveillance Net- t-test for continuous variables; statistical significance
work of Communicable Disease (NSNCD). was defined as P < 0.05. The association between
DOT and treatment outcomes at the end of 12 months
Data collection was examined using multivariate analyses. Factors
All TB cases, both suspected and confirmed, are noti- were entered into models based on biological plausi-
fiable by law to the Taiwan Centers for Disease Con- bility, previous literature and statistical significance
trol (CDC) via the NSNCD. Standardized demo- in bivariate analysis. Colinearity and interactions were
graphic, clinical, bacteriological and treatment data assessed. Stepwise logistic regression was used to con-
are entered directly into the national database by pub- struct a model to control for covariates associated
lic health staff from routine medical and laboratory with DOT and unsuccessful treatment outcomes, us-
records. Information on DOT and treatment out- ing odds ratios (ORs) and 95% confidence intervals
comes is also recorded in the NSNCD. (CIs). We used the Hosmer-Lemeshow test to evalu-
This analysis underwent ethical review by the US ate goodness-of-fit and the likelihood ratio test to
CDC; it was determined to be a program evaluation select the best fitting models. A multivariable Cox
activity, not human subjects research. proportional hazards model was used to assess the
independent relationship between proportion of DOT
Definitions and mortality.
A patient was classified as a DOT case if he/she had
been evaluated by a treating physician, signed a writ- RESULTS
ten consent form and had an official DOT observer
witness the ingestion of anti-tuberculosis medicines, Study population
as documented in the NSNCD. We defined percent- Among 12 867 new consenting TB cases documented
age of days on DOT as the number of days of DOT as being part of the DOT program in the national TB
by a DOT observer recorded in the daily log divided registry and starting treatment between 1 January
by the total number of days on treatment. In cases 2007 and 30 June 2008, 1339 were excluded: 101
where a patient had more than one daily log entry with extra-pulmonary disease, 173 with drug resis-
for DOT in one day, we counted one visit per day in tance, 176 with missing days on treatment, 5 who
the calculation. We categorized this variable into moved out of the country, 221 who did not have TB
three groups—zero DOT, between zero and 60%, and 760 who were still on treatment or had no treat-
and >60% DOT—based on the median percentage ment outcomes recorded at the end of 12 months
(60.6%) for those with any DOT. Patients’ outcomes (some cases had more than one exclusion criteria). A
were classified according to WHO categories.20 Suc- total of 11 528 cases remained in the analysis. The
464 The International Journal of Tuberculosis and Lung Disease

majority were male (72%), and the median age was ment was 205 (range 8–365) for >60% DOT, 210
67 years (range 1–96). (range 6–365) for ⩽60% DOT and 68 (range 0–365)
for no DOT.
Directly observed therapy
Among 11 528 patients initiating treatment, the per- Treatment outcomes
centage of days on which they received DOT was Proportion of DOT was strongly associated with
>60% for 5150 (45%), ⩽60% for 4601 (40%) treatment outcomes. Among patients with unsuccess-
and zero for 1777 (15%; Table 1). A greater propor- ful outcomes, respectively 5%, 40% and 55% had
tion of cases with no DOT were older, male or ini- >60% DOT, ⩽60% DOT and no DOT (P < 0.0001;
tially treated with a non-WHO-recommended regi- Table 2). All socio-demographic, diagnostic and treat-
men. DOT was significantly associated with smear ment characteristics in Table 2 were statistically sig-
and culture status and cavitary disease, indicators of nificant in their bivariate associations with treatment
disease severity at the time of diagnosis. Specifically, outcomes. The median number of days on treatment
patients with no DOT had the highest proportions of was 215 (range 154–365) for those with successful
both positive smear and culture, and patients receiv- outcomes and 60 (range 0–365) for those with un-
ing any DOT were more likely to have cavitary dis- successful outcomes (P < 0.0001).
ease than those with no DOT. More DOT was associ- In the multivariable logistic regression model, com-
ated with any report of an adverse event, specifically pared with patients who had >60% DOT, patients
nausea or vomiting, during treatment, whereas num- who received no DOT were much more likely to have
ber of hospitalizations was higher in patients with unsuccessful treatment outcomes after 12 months (ad-
less or no DOT. The median number of days on treat- justed OR [aOR] 73.1, 95%CI 58.9–90.6) (Table 2).

Table 1 Characteristics of new pulmonary tuberculosis patients by proportion of DOT*


>60% DOT ⩽60% DOT No DOT Total
(n = 5150) (n = 4601) (n = 1777) (N = 11 528)
Characteristic n (%) n (%) n (%) n (%)
Socio-demographic
Age at diagnosis, years
⩽24 360 (7.0) 295 (6.4) 20 (1.1) 675 (5.9)
25–44 908 (17.6) 737 (16.0) 105 (5.9) 1 750 (15.2)
45–64 1501 (29.2) 1165 (25.3) 325 (18.3) 2 991 (25.9)
⩾65 2381 (46.2) 2404 (52.3) 1327 (74.7) 6 112 (53.0)
Sex
Female 1554 (30.2) 1288 (28.0) 438 (24.7) 3 280 (28.5)
Male 3596 (69.8) 3313 (72.0) 1339 (75.3) 8 248 (71.5)
Living in a mountainous region†
No 4952 (96.2) 4372 (95.0) 1755 (98.8) 11 079 (96.1)
Yes 198 (3.8) 229 (5.0) 22 (1.2) 449 (3.9)
Diagnosis
Bacteriology results
Smear- and culture-negative 125 (2.4) 340 (7.4) 32 (1.8) 497 (4.4)
Smear- and culture-positive 3119 (60.9) 2337 (51.2) 1067 (61.2) 6 523 (57.0)
Smear- or culture-positive 1880 (36.7) 1890 (41.4) 644 (37.0) 4 414 (38.6)
Cavitary disease
Normal CXR 117 (2.3) 105 (2.3) 57 (3.2) 279 (2.4)
Abnormal CXR and no cavity present 3666 (71.9) 3376 (74.0) 1396 (79.4) 8 438 (73.9)
Abnormal CXR and cavity present 1313 (25.8) 1081 (23.7) 306 (17.4) 2 700 (23.7)
Treatment
Initial treatment prescribed
Other regimens 573 (11.1) 690 (15.0) 439 (24.7) 1 702 (14.8)
WHO-recommended regimen 4577 (88.9) 3911 (85.0) 1338 (75.3) 9 826 (85.2)
Any report of adverse event
No 4517 (87.7) 4094 (89.0) 1741 (98.0) 10 352 (89.8)
Yes 633 (12.3) 507 (11.0) 36 (2.0) 1 176 (10.2)
Number of hospitalizations during treatment
0 2867 (55.7) 1374 (29.9) 172 (10.0) 4 413 (38.5)
1 2015 (39.1) 2044 (44.5) 1229 (71.4) 5 288 (46.1)
⩾2 267 (5.2) 1175 (25.6) 321 (18.6) 1 763 (15.4)
Treatment outcome at end of 1 year
Unsuccessful treatment 116 (2.3) 877 (19.1) 1191 (67.0) 2 184 (19.0)
Successful treatment 5034 (97.8) 3724 (80.9) 586 (33.0) 9 344 (81.0)
* All socio-demographic, diagnostic and treatment characteristics in Table 1 are significant in bivariate associations with DOT based on the χ2 test (P < 0.05).
Cell counts do not always sum to column total due to missing data. Missing data were excluded when missing data for all of the cell percentages across all
categories comprised <2%.
† Proxy measure for indigenous populations and hard-to-reach areas.

DOT = directly observed therapy; CXR = chest radiograph.


DOT and treatment outcomes in Taiwan 465

Table 2 Factors associated with unsuccessful treatment outcomes in bivariate analysis and the multivariate logistic regression
model (N = 11 528)*
Successful Unsuccessful
treatment treatment
(n = 9344) (n = 2184)
Characteristic n (%) n (%) OR (95%CI) aOR (95%CI)
Age at diagnosis, years
⩽24 664 (7.1) 11 (0.5) 1.0 1.0
25–44 1662 (17.8) 88 (4.0) 3.2 (1.7–6.0) 2.5 (1.3–4.8)
45–64 2676 (28.6) 315 (14.4) 7.1 (3.9–13.0) 4.7 (2.5–8.9)
⩾65 4342 (46.5) 1770 (81.1) 24.6 (13.5–44.8) 15.1 (8.2–27.8)
Sex
Female 2745 (29.4) 535 (24.5) 1.0 1.0
Male 6599 (70.6) 1649 (75.5) 1.3 (1.2–1.4) 1.2 (1.1–1.4)
Living in a mountainous region
No 8945 (95.7) 2134 (97.7) 1.0
Yes 399 (4.3) 50 (2.3) 0.5 (0.4–0.7)
Bacteriology results
Smear- and culture-negative 438 (4.7) 59 (2.8) 1.0 1.0
Smear- and culture-positive 5241 (56.4) 1282 (59.8) 1.8 (1.4–2.4) 2.0 (1.5–2.7)
Smear- or culture-positive 3613 (38.9) 801 (37.4) 1.6 (1.2–2.2) 1.5 (1.1–2.0)
Cavitary disease
Normal CXR 223 (2.4) 56 (2.6) 1.0
Abnormal CXR and no cavity present 6688 (72.3) 1750 (80.8) 1.0 (0.8–1.4)
Abnormal CXR and cavity present 2341 (25.3) 359 (16.6) 0.6 (0.5–0.8)
Initial treatment prescribed
Other regimens 1172 (12.5) 530 (24.3) 1.0 1.0
WHO-recommended regimen 8172 (87.5) 1654 (75.7) 0.5 (0.4–0.5) 0.7 (0.6–0.8)
Any report of adverse event
No 8291 (88.7) 2061 (94.4) 1.0
Yes 1053 (11.3) 123 (5.6) 0.5 (0.4–0.6)
Number of hospitalizations during treatment
0 4198 (44.9) 215 (10.1) 1.0
1 3936 (42.1) 1352 (63.8) 6.7 (5.8–7.8)
⩾2 1210 (13.0) 553 (26.1) 8.9 (7.5–10.6)
Proportion of days of DOT
>60% DOT 5034 (53.9) 116 (5.3) 1.0 1.0
⩽60% DOT 3724 (39.9) 877 (40.2) 10.2 (8.4–12.5) 10.7 (8.7–13.2)
No DOT 586 (6.3) 1191 (54.5) 88.2 (71.6–108.7) 73.1 (58.9–90.6)
* All socio-demographic, diagnostic and treatment characteristics in Table 2 are significant in bivariate associations with DOT based on the χ2 test (P < 0.05).
Cell counts do not always sum to column total due to missing data. Missing data were excluded when missing data for all of the cell percentages across all
categories comprised <2%.
† Proxy measure for indigenous populations and hard-to-reach areas.

OR = odds ratio; aOR = adjusted OR; CI = confidence interval; CXR = chest radiograph; DOT = directly observed therapy.

The effect was similar, but less dramatic, for patients aOR 53.7, 95%CI 43.1–66.8; ⩽60% DOT: aOR
with ⩽60% DOT (aOR 10.7, 95%CI 8.7–13.2). In- 10.6, 95%CI 8.7–13.1). In a proportional hazards
creasing age, male sex and having a positive smear analysis, a similar dose-response effect was found be-
and/or culture were associated with unsuccessful treat- tween proportion of DOT and death, after control-
ment outcome, whereas having a WHO-recommended ling for age, sex, bacteriology results and initial treat-
initial treatment regimen was associated with suc- ment. Receiving no DOT (adjusted hazard ratio [aHR]
cessful outcome. 53.9, 95%CI 43.0–67.4) and ⩽60% DOT (aHR 10.9,
To look for a threshold effect, we further exam- 95%CI 8.7–13.6) significantly increased the risk of
ined the distribution of DOT by deciles; at approxi- death compared with receiving >60% DOT.
mately 40–50% DOT, 84% of TB cases achieved
treatment success, near the WHO target of 85% treat-
DISCUSSION
ment success.
Death during TB treatment occurred in 2030 In this national-level study, we quantified DOT for
(17.6%) patients. To evaluate the impact of early each patient on anti-tuberculosis treatment in a large
deaths on unsuccessful outcomes, we excluded 344 programmatic setting. The most important factor
(3%) patients who died during the first 2 weeks of associated with treatment outcomes was proportion
treatment from the logistic regression analysis. The of DOT. Among new pulmonary TB cases, a dose-
association between proportion of DOT and unsuc- response effect was observed: increased DOT was
cessful treatment outcomes remained similar (no DOT: strongly associated with better treatment outcomes,
466 The International Journal of Tuberculosis and Lung Disease

after controlling for other factors. These findings high- that DOT was provided to patients but not docu-
light the importance of DOT in improving treatment mented. Also, many patients do not receive DOT dur-
outcomes in Taiwan. The provision of standardized ing the weekends; at most they would receive DOT 5
treatment with supervision and patient support is a out of 7 days per week (>71% of the time). The DOT
key component of the Stop TB strategy.1 DOT can categorization used in this analysis would still clas-
help ensure patients adhere to and complete lengthy sify these cases as >60%, and therefore our findings
and complex TB treatment regimens. By reducing poor are able to take this into account. As this was an ob-
treatment outcomes, such as default, DOT can ulti- servational study in a large programmatic setting, it
mately help to reduce the spread of infection, the risk was not feasible to measure all confounders, includ-
of acquired drug resistance and the development of ing some individual characteristics, such as alcohol
new cases.9,22 An important area of research would and drug use, and homelessness. Human immuno-
be to examine the risk of recurrence among patients deficiency virus (HIV) status was not assessed; how-
with and without DOT in Taiwan. ever, due to the small proportion (0.7%) of TB patients
Based on our criteria, among patients in the DOT estimated to have HIV infection in Taiwan, it is un-
program initiating TB treatment, 15% did not have likely that HIV status would have greatly influenced
any DOT recorded. These findings highlight the chal- the conclusions.30 Furthermore, we were unable to
lenges faced by TB control programs when imple- evaluate the quality of care (e.g., DOT observer skills,
menting and widening the reach of DOT nation- or relationship between DOT observer and patient).
wide, while simultaneously maintaining high-quality In Taiwan, where DOT observers receive training and
services in all sectors of society.23 A greater propor- close supervision and have a reasonable case load,
tion of patients who were older, male or who started the quality of DOT is likely to influence outcomes, al-
treatment with a non-standard regimen did not re- though this was not assessed in this study.
ceive DOT. Understanding who is not receiving DOT A strength of this study is that it is a large,
can help identify high-risk patients and ensure that national-level analysis examining the impact of DOT
they receive additional treatment support. Innovative on treatment outcomes in a programmatic setting
strategies have been implemented in Taiwan to sup- with sufficient sample size to control for potential
port TB patients and clinicians with DOT, including a confounding and assess different criteria for the pro-
lottery program that rewards patients for taking their portion of DOT.
medications by providing opportunities for monetary
incentives, and a remuneration scheme set up by the
CONCLUSION
Bureau of National Health Insurance for clinicians
treating TB patients.24 DOT is a practical and implementable approach with-
In addition to proportion of DOT during treatment, in the Stop TB strategy. Combined with strong politi-
other factors associated with poor treatment outcomes cal commitment, including promotion of innovative
in Taiwan were older age, male sex, having both a strategies that improve case notification and treat-
positive smear and culture and receiving a non-WHO- ment outcomes, and an exemplary information sys-
recommended regimen at baseline. These findings are tem that tracks the progress of every patient and fa-
consistent with smaller studies from Taiwan that have cilitates accountability and evaluation, such as those in
previously found that being older,25,26 male27 and Taiwan, effective TB control is feasible.31 These find-
positive bacteriology at baseline27 are predictive of ings help to improve our understanding and highlight
poor treatment outcomes among pulmonary TB pa- the importance of ensuring universal DOT in Taiwan.
tients. Although data were only available for the initial
Disclaimer: The findings and conclusions in this report are those
treatment regimen, it is not clear why, for almost
of the authors and do not necessarily represent the official position
15% of cases, a non-WHO-recommended regimen of the US Centers for Disease Control and Prevention.
was used in Taiwan. However, these findings are sim-
ilar to a 2007 study in which up to 15% of regimens
were found not to comply with recommendations References
to prescribe the standardized four drug regimen.28 1 World Health Organization. The Stop TB Strategy: building on
In response, Taiwan CDC reduced reimbursements and enhancing DOTS to meet the TB-related Millennium De-
velopment Goals. WHO/HTM/TB/2006.368. Geneva, Switzer-
for suboptimal regimens, and prescriptions of non-
land: WHO, 2006. http://whqlibdoc.who.int/hq/2006/WHO_
standardized regimens fell to 5% in 2008.29 HTM_STB_2006.368_eng.pdf Accessed January 2012.
There were several limitations in this study. As 2 Stop TB Partnership. The Global Plan to Stop TB, 2006–2015.
only TB cases reported to the NSNCD were included, Actions for life: towards a world free of tuberculosis. WHO/
this analysis missed TB cases who were not registered HTM/STB/2006.35. Geneva, Switzerland: WHO, 2006. http://
whqlibdoc.who.int/publications/2006/9241593997_eng.pdf
in the system. No formal evaluation was performed
Accessed January 2012.
to assess whether the DOT data in the NSNCD are 3 World Health Organization. Forty-fourth World Health As-
accurate. Furthermore, the absence of data does not sembly, resolutions and decisions. Resolution WHA 44.8. Ge-
always signify the absence of services: it is possible neva, Switzerland: WHO, 1991.
DOT and treatment outcomes in Taiwan 467

4 World Health Organization. Global tuberculosis control. Tuberculosis epidemiology and directly observed treatment,
WHO report 2010. WHO/HTM/TB/2010.7. Geneva, Switzer- short course (DOTS) strategy report. Taipei, ROC: Centers for
land: WHO, 2010. http://www.who.int/tb/publications/global_ Disease Control, Department of Health, 2007.
report/2010/en/index.html Accessed January 2012. 18 Hsu C B, Lo H Y, Lee C Y, Yang S L, Wang K F, Yang S Y. Pre-
5 World Health Organization. WHO annual report 2009. liminary evaluation of Taiwan’s tuberculosis DOTS strategy,
Global tuberculosis control—epidemiology, strategy, financing. Centers for Disease Control, Department of Health. Taiwan
WHO/HTM/TB/2009.411. Geneva, Switzerland: WHO, 2009. Epidemiol Bull 2008; 24: 230–253.
http://www.who.int/tb/publications/global_report/2009/en/ 19 Department of Health, Taiwan, Executive Yuan. Mobilization
index.html Accessed January 2012. plan to reduce tuberculosis in half in ten years. No 0950031290.
6 American Thoracic Society/US Centers for Disease Control and Taipei, Taiwan: Department of Health, 2006.
Prevention/Infectious Diseases Society of America. Treatment of 20 World Health Organization. Treatment of tuberculosis: guide-
tuberculosis. MMWR Recomm Rep 2003; 52 (RR-11): 1–77. lines for national programmes. 3rd ed. WHO/CDS/TB.2003.313.
7 Sbarbaro J. What are the advantages of direct observation of Geneva, Switzerland: WHO, 2003. http://whqlibdoc.who.int/hq/
treatment? In: Frieden T, ed. Toman’s tuberculosis: case detec- 2003/who_cds_tb_2003.313_eng.pdf Accessed January 2012.
tion, treatment, and monitoring: questions and answers. 2nd ed. 21 Zignol M, Wright A, Jaramillo E, Nunn P, Raviglione M C.
Geneva, Switzerland: WHO, 2004: pp 183–184. Patients with previously treated tuberculosis: no longer ne-
8 World Health Organization, International Union Against Tu- glected. Clin Infect Dis 2007; 44: 61–64.
berculosis and Lung Disease, Royal Netherlands Tuberculosis 22 Centers for Disease Control and Prevention. Initial therapy for
Association. Revised international definitions in tuberculosis tuberculosis in the era of multidrug resistance: recommenda-
control. Int J Tuberc Lung Dis 2001; 5: 213–215. tions of the Advisory Council for the Elimination of Tubercu-
9 Chaulk C P, Kazandjian V A. Directly observed therapy for losis. MMWR Morb Mortal Wkly Rep 1993; 42 (RR-7): 1–8.
treatment completion of pulmonary tuberculosis consensus 23 Wu P S, Chou P, Chang N T, Sun W J, Kuo H S. Assessment of
statement of the public health tuberculosis guidelines panel. changes in knowledge and stigmatization following tuberculo-
JAMA 1998; 279: 943–948. sis training workshops in Taiwan. J Formos Med Assoc 2009;
10 China Tuberculosis Control Collaboration. Results of directly 108: 377–385.
observed short-course chemotherapy in 112 842 Chinese pa- 24 Li Y H, Tsai W C, Khan M, et al. The effects of pay-for-
tients with smear-positive tuberculosis. Lancet 1996; 23; 347: performance on tuberculosis treatment in Taiwan. Health Pol-
835–836. icy Plan 2010; 25: 334–341.
11 Chung W-S, Chang Y-C, Yang M-C. Factors influencing the 25 Chiang C-Y, Lee J-J, Yu M-C, Enarson D A, Lin T-P, Luh K-T.
successful treatment of infectious pulmonary tuberculosis. Int J Tuberculosis outcomes in Taipei: factors associated with treat-
Tuberc Lung Dis 2007; 11: 59–64. ment interruption for 2 months and death. Int J Tuberc Lung
12 Zwarenstein M, Schoeman J, Vundule C, Lombard C, Tatley Dis 2009; 13: 105–111.
M. Randomised controlled trial of self-supervised and directly 26 Wang C S, Chen H C, Yang C J, et al. The impact of age on the
observed treatment of tuberculosis. Lancet 1998; 352: 1340– demographic, clinical, radiographic characteristics and treat-
1343. ment outcomes of pulmonary tuberculosis patients in Taiwan.
13 Walley J D, Khan M A, Newell J N, Khan M H. Effectiveness Infection 2008; 36: 335–340.
of the direct observation component of DOTS for tuberculosis: 27 Lee J J, Wu R L, Lee Y S, Wu Y C, Chiang C Y. Treatment out-
a randomized controlled trial in Pakistan. Lancet 2001; 357: come of pulmonary tuberculosis in eastern Taiwan—experience
664–669. at a medical center. J Formos Med Assoc 2007; 106: 25–30.
14 Becx-Bleumink M, Djamaluddin S, Loprang F, de Soldenhoff 28 Chan P-C, Hsu C-B, Lin H-C, et al. The deviation from stan-
R, Wibowo H, Aryono M. High cure rates in smear-positive dardized treatment regimen in 108 randomly selected smear
tuberculosis patients using ambulatory treatment with once- positive tuberculosis patients. Taiwan Epidemiol Bull 2008; 24:
weekly supervision during the intensive phase in Sulawesi, Re- 254–263.
public of Indonesia. Int J Tuberc Lung Dis 1999; 3: 1066–1072. 29 Li Y-P, Chan P-C, Wang K-F, Yang C-H, Kuo H-S. Introduction
15 Volmink J, Garner P. Directly observed therapy for treating tu- of reducing reimbursement from NHI to improve the inade-
berculosis. Cochrane Database Syst Rev 2007; (4): CD003343. quate regimen for TB control. Int J Tuberc Lung Dis 2009; 13
16 Centers for Disease Control, Department of Health, Taiwan. (Suppl 1): S107.
Taiwan tuberculosis control report 2009. Taipei, ROC: Cen- 30 Centers for Disease Control, Department of Health, Taiwan.
ters for Disease Control, Department of Health, 2009. http:// Taiwan tuberculosis control report 2010. Taipei, Taiwan: CDC,
www.cdc.gov.tw/public/data/011310555271.pdf Accessed Jan- 2010.
uary 2012. 31 Frieden T R. Lessons from tuberculosis control for public
17 Centers for Disease Control, Department of Health, Taiwan. health. Int J Tuberc Lung Dis 2009; 13: 421–428.
DOT and treatment outcomes in Taiwan i

RÉSUMÉ

C O N T E X T E : Le traitement directement observé (DOT) lesquels un observateur officiel du DOT a été témoin du
est un élément-clé du traitement de la tuberculose (TB) traitement est > 60% chez 5150 patients (45%) et ⩽60%
et des efforts de lutte. A Taïwan, le DOT a été mis en chez 4601 patients (40%), alors que chez 1777 patients
œuvre en 2006, moment où la stratégie Stop TB a été (15%) aucun jour de traitement observé n’a été enregis-
adoptée comme politique nationale. tré. Les facteurs liés de manière indépendante à des ré-
O B J E C T I F : Quantifier le DOT au niveau national chez sultats de traitement non couronnés de succès et à la
les patients sous traitement TB et mesurer l’association mortalité sont l’âge plus avancé, le sexe masculin, les ré-
entre la quantité de DOT et les résultats du traitement sultats positifs de l’examen bactériologique et l’admini-
TB. stration dès le début d’un régime de traitement non re-
S C H É M A : Nous avons analysé de manière prospective commandé par l’Organisation Mondiale de la Santé. On
les données colligées sur l’ensemble des nouveaux cas de a trouvé un rapport dose-effet entre la proportion de
TB pulmonaire déclarés au registre national relié à in- DOT et ces résultats.
ternet entre le 1er janvier 2007 et le 30 juin 2008. Nous C O N C L U S I O N : Ces observations soulignent l’impor-
avons comparé dans des analyses multivariées les résul- tance d’assurer un DOT universel si l’on veut améliorer
tats du traitement et la quantité de DOT. les résultats du traitement chez les nouveaux patients at-
R É S U LTAT S : Parmi 11 528 patients commençant un teints de TB pulmonaire.
traitement de la TB, la proportion de jours pendant

RESUMEN

MARCO DE REFERENCIA: El tratamiento directamente tratamiento antituberculoso, la proporción de días en


observado (DOT) constituye un elemento central de los los cuales un observador oficial de DOT presenció la
programas de control y tratamiento de la tuberculosis administración del tratamiento fue >60% en 5150 pa-
(TB). En Taiwán, el DOT se introdujo en el 2006 cuando cientes (45%) e ⩽60% en 4601 pacientes (40%), pero
se adoptó la iniciativa Alto a la Tuberculosis como una en 1777 pacientes (15%) no se encontró el registro de
política nacional. DOT. Los factores que se asociaron en forma indepen-
O B J E T I V O : Cuantificar la aplicación del DOT en los diente con el fracaso terapéutico y la mortalidad fueron
pacientes que se encontraban en tratamiento antituber- la ancianidad, el sexo masculino y en forma simultánea
culoso y medir la correlación entre la cantidad de dosis haber tenido resultados bacteriológicos positivos y reci-
recibidas con DOT y los desenlaces terapéuticos a escala bido un tratamiento diferente del recomendado por la
nacional en Taiwán. Organización Mundial de la Salud al comienzo. Se en-
M É T O D O : Se analizaron de manera prospectiva los da- contró un efecto de dosis y respuesta entre la propor-
tos recogidos sobre todos los casos nuevos de TB notifi- ción de la aplicación de DOT y estos desenlaces.
cados por internet al registro nacional entre el 1° de en- C O N C L U S I Ó N : Los resultados del presente estudio de-
ero del 2007 y el 30 de junio del 2008. En los análisis stacan la importancia de la aplicación universal del DOT
multifactoriales se compararon los desenlaces terapéuti- en el mejoramiento de los desenlaces terapéuticos de los
cos y la proporción de dosis recibidas con DOT. casos nuevos de TB pulmonar.
R E S U LTA D O S : En los 11 528 pacientes que iniciaron el

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