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Sistemas de recordatorio e intervenciones para rescatar pacientes inasistentes para el diagnóstico y tratamiento de la tuberculosis

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Referencias

Referencias de los estudios incluidos en esta revisión

Cheng 1997 {published data only}

Cheng TL, Ottolini MC, Baumhaft K, Brasseux C, Wolf MD, Scheidt PC. Strategies to increase adherence with tuberculin test reading in a high‐risk population. Pediatrics 1997;100(2):210‐3.

Krishnaswami 1981 {published data only}

Krishnaswami KV, Somasundaram PR, Tripathy SP, Vaidyanathan B, Radhakrishna S, Fox WA. Randomised study of two policies for managing default in out‐patients collecting supplies of drugs for pulmonary tuberculosis in a large city in South India. Tubercle 1981;62(2):103‐12.

Mohan 2003 {published data only}

Mohan A, Nassir H, Niazi A. Does routine home visiting improve the return rate and outcome of DOTS patients who delay treatment?. Eastern Mediterranean Health Journal 2003;9(4):702‐8.

Paramasivan 1993 {published data only}

Paramasivan R, Parthasarathy RT, Rajasekaran S. Short course chemotherapy: A controlled study of indirect defaulter retrieval method. Indian Journal of Tuberculosis 1993;40(4):185‐90.

Roberts 1983i {published data only}

Roberts MC. Wurtele SK. Leeper JD. Experiments to increase return in a medical screening drive: two futile attempts to apply theory to practice. Social Science & Medicine 1983;17(11):741‐6.

Roberts 1983ii {published data only}

Roberts MC. Wurtele SK. Leeper JD. Experiments to increase return in a medical screening drive: two futile attempts to apply theory to practice. Social Science & Medicine 1983;17(11):741‐6.

Sanmarti 1993 {published data only}

Sanmarti LS, Megias JA, Gomez MN, Soler JC, Alcala EN, Sune MR, et al. Evaluation of the efficacy of health education on the compliance with antituberculosis chemoprophylaxis in school children. A randomized clinical trial. Tubercle and Lung Disease 1993;74(1):28‐31.

Tanke 1994 {published data only}

Tanke ED, Leirer VO. Automated telephone reminders in tuberculosis care. Medical Care 1994;32(4):380‐89.

Tanke 1994: diagnosis arm {published data only}

See Tanke 1994.

Tanke 1994: prophylaxis arm {published data only}

See Tanke 1994.

Tanke 1994: treatment arm {published data only}

See Tanke 1994.

Tanke 1997 {published data only}

Tanke ED, Martinez CM, Leirer VO. Use of automated reminders for tuberculin skin test return. American Journal of Preventive Medicine 1997;13(3):189‐92.

Referencias de los estudios excluidos de esta revisión

AL‐Hajjaj 2000 {published data only}

Al‐Hajjaj MS, Al‐Khatim IM. High rate of non‐compliance with anti‐tuberculosis treatment despite a retrieval system: a call for implementation of directly observed therapy in Saudi Arabia. International Journal of Tuberculosis and Lung Disease 2000;4(4):345‐9.

Alcaide Megías 1990 {published data only}

Alcaide Megías J, Altet Gómez MN, Canela Soler J, Serra Majen L, Garrido Morales P, Navas Alcalá E, et al. Influence of health education on compliance with antituberculous chemoprophylaxis in children: a community trial [Influencia de la educaci¨®n sanitaria en el cumplimiento de la quimioprofilaxis antituberculosa en ninos: ensayo comunitario]. Revista Clínica Española 1990;187(2):89‐93.

Bordley 2001 {published data only}

Bordley WC, Margolis PA, Stuart J, Lannon C, Keyes L. Improving preventive service delivery through office systems. Pediatrics 2001;108(3):41‐8.

Gordillo 2003 {published data only}

Gordillo AGC, Gordillo AJF, Jimenez DJ.E. Educational strategy for improving patient compliance with the tuberculosis treatment regimen in Chiapas, Mexico [Estrategia educativa para incrementar el cumplimiento del regimen antituberculoso en Chiapas, Mexico]. Pan American Journal of Public Health 2003;14(6):402‐8.

Hovell 2003 {published data only}

Hovell MF, Sipan CL, Blumberg EJ, Hofstetter CR, Slymen D, Friedman L, et al. Increasing Latino adolescents' adherence to treatment for latent tuberculosis infection: a controlled trial. American Journal of Public Health 2003;93(11):1871‐7.

Jin 1993 {published data only}

Jin BW, Kim SC, Mori T, Shimao T. The impact of intensified supervisory activities on tuberculosis treatment. Tubercle and Lung Disease 1993;74(4):267‐72.

Krishna 2002 {published data only}

Krishna S, Balas EA, Boren SA, Maglaveras N. Patient acceptance of educational voice messages: a review of controlled clinical studies. Methods of Information in Medicine 2002;41(5):360‐9.

Lin 2006 {published data only}

Lin RL, Lin FJ, Wu CL, Peng MJ, Chen PJ, Kuo HT. Effect of a hospital‐based case management approach on treatment outcome of patients with tuberculosis. Journal of the Formosan Medical Association 2006;105(8):636‐44.

Morisky 1990 {published data only}

Morisky DE, Malotte CK, Choi P, Davidson P, Rigler S, Sugland B, et al. A patient education program to improve adherence rates with antituberculosis drug regimens. Health Education Quarterly 1990;17(3):253‐67.

Morisky 2001 {published data only}

Morisky DE, Malotte CK, Ebin V, Davidson P, Cabrera D, Trout PT, et al. Behavioral interventions for the control of tuberculosis among adolescents. Public Health Reports 2001;116(6):568‐74.

Nyamathi 2007 {published data only}

Nyamathi A. Stein JA. Schumann A, Tyler D. Latent variable assessment of outcomes in a nurse‐managed intervention to increase latent tuberculosis treatment completion in homeless adults. Health Psychology 2007;26(1):68‐76.

Thiam 2007 {published data only}

Thiam S, LeFevre AM, Hane F, Ndiaye A, Ba F, Fielding KL, et al. Effectiveness of a strategy to improve adherence to tuberculosis treatment in a resource‐poor setting: a cluster randomized controlled trial. JAMA 2007;297(4):380‐6.

Referencias adicionales

Bosch Capblanch 2007

Bosch‐Capblanch X, Abba K, Prictor M, Garner P. Contracts between patients and healthcare practitioners for improving patients' adherence to treatment, prevention and health promotion activities. Cochrane Database of Systematic Reviews 2007, Issue 2. [DOI: 10.1002/14651858.CD004808.pub3]

Goble 1993

Goble M, Iseman MD, Madsen LA. Treatment of 171 patients with pulmonary tuberculosis resistant to isoniazid and rifampin. New England Journal of Medicine 1993;328(8):527‐32.

Green 2003

Green D. ICT‐enabled development case studies series: The compliance service uses SMS technology for TB treatment. www.bridges.org/case_studies/137 2003 (accessed 1 September 2006).

Haynes 2008

Haynes RB, Ackloo E, Sahota N, McDonald HP, Yao X. Interventions for enhancing medication adherence. Cochrane Database of Systematic Reviews 2008, Issue 2. [DOI: 10.1002/14651858.CD000011.pub3]

Jagota 1996

Jagota P, Sreenivas TR, Parimala N. Improving treatment compliance by observing difference in treatment irregularity. Indian Journal of Tuberculosis 1996;43:75‐80.

Johansson 1999

Johansson E, Long NH, Diwan VK, Winkvist A. Attitudes to compliance with tuberculosis treatment among women and men in Vietnam. International Journal of Tuberculosis and Lung Disease 1999;3(10):862‐8.

Jüni 2001

Jüni P, Altman DG, Egger M. Systematic reviews in health care: Assessing the quality of controlled clinical trials. BMJ 2001;323(7303):42‐6.

Lefebvre 2006

Lefebvre C, Manheimer E, Glanville J. Chapter 6: Searching for studies. In: Higgins JPT, Green S (editors). Cochrane Handbook for Systematic Reviews of Interventions Version 5.0.0 (updated February 2008). The Cochrane Collaboration, 2008.. Available from www.cochrane‐handbook.org.

M'Imunya 2007

M'Imunya MJ, Volmink J. Education and counselling for promoting adherence to the treatment of active tuberculosis. Cochrane Database of Systematic Reviews 2007, Issue 3. [DOI: 10.1002/14651858.CD006591]

Mitchison 1998

Mitchison DA. How drug resistance emerges as a result of poor compliance during short course chemotherapy for tuberculosis. International Journal of Tuberculosis and Lung Disease 1998;2(1):10‐5.

O'Boyle 2002

O'Boyle SJ, Power JJ, Ibrahim MY, Watson JP. Factors affecting patient compliance with anti‐tuberculosis chemotherapy using the directly observed treatment, short‐course strategy (DOTS). International Journal of Tuberculosis and Lung Disease 2002;6(4):307‐12.

Ormerod 1991

Ormerod LP, Prescott RJ. Inter‐relations between relapses, drug regimens and compliance with treatment in tuberculosis. Respiratory Medicine 1991;85(3):239‐42.

Review Manager 5 [Computer program]

The Nordic Cochrane Centre, The Cochrane Collaboration. Review Manager (RevMan). Version 5.0. Copenhagen: The Nordic Cochrane Centre, The Cochrane Collaboration, 2008.

Thilakavathi 1993

Thilakavathi S, Fredrick JS, Fredrick KG, Parthasarathy R, Santha T. High coverage for long term follow‐up of patients with spinal tuberculosis. Indian Journal of Tuberculosis 1993;40(2):91‐4.

Vann 2005

Jacobson Vann JC, Szilagyi P. Patient reminder and recall systems to improve immunization rates. Cochrane Database of Systematic Reviews 2005, Issue 3. [DOI: 10.1002/14651858.CD003941.pub2]

Volmink 2007

Volmink J, Garner P. Directly observed therapy for treating tuberculosis. Cochrane Database of Systematic Reviews 2007, Issue 4. [DOI: 10.1002/14651858.CD003343.pub3]

Weis 1994

Weis SE, Slocum PC, Blais FX, King B, Nunn M, Matney GB, et al. The effect of directly observed therapy on the rates of drug resistance and relapse in tuberculosis. New England Journal of Medicine 1994;330(17):1179‐84.

WHO 2003a

WHO Global Tuberculosis Programme. Treatment of tuberculosis: guidelines for national programmes [WHO/CDS/TB/2003.313]. 3rd Edition. Geneva: World Health Organization, 2003.

WHO 2003b

World Health Organization. Adherence to long term therapies: evidence for action. Geneva, Switzerland: World Health Organization, 2003.

WHO 2006

World Health Organization, Communicable Diseases Cluster. Global tuberculosis control: surveillance, planning, financing : WHO report 2006 [WHO/HTM/TB/2006.362]. Geneva: World Health Organization, 2006.

WHO 2007

World Health Organization. Global tuberculosis control: surveillance, planning, financing. WHO Report 2007. WHO/HTM/TB/2007.376. Geneva: World Health Organization, 2007.

WHO 2008

WHO/IUATLD Global Project on Anti‐tuberculosis Drug Resistance Surveillance 2002?2007. Anti‐tuberculosis drug resistance in the world. Report No. 4. Geneva, Switzerland: World Health Organization, 2008.

Characteristics of studies

Characteristics of included studies [ordered by study ID]

Cheng 1997

Methods

Quasi‐randomized controlled trial

Generation of allocation sequence: randomized by day of the week

Allocation concealment: unclear

Blinding of outcome assessors: unclear

Blinding of providers and participants: not possible

Inclusion of randomized participants in the analysis: 627/627 (100%)

Protection against contamination: unclear

Participants

Number: 627 randomized

Inclusion criteria: consecutive children ages 1 to 12 years due for a tuberculosis test in an urban children's hospital outpatient department; 1 child per family enrolled

Exclusion criteria: not stated

Interventions

Intervention of interest
1. Reminder phone call (reminders included a written information sheet with the times to return; skin tests circled in permanent marker and date of return stamped on mother's and child's hands)

Other interventions
2. Positive reinforcement group (transportation tokens and toy on return)
3. Negative reinforcement group (asked to leave school forms until they returned for test reading and were told that the test would be repeated if not read on time)
4. Parents trained to read the Mantoux tuberculosis test for induration or no induration, and a nurse home visit was scheduled to verify results

Control
5. Routine verbal and written instructions

All families received education regarding the importance of skin testing for tuberculosis and the need for follow up to read the results. Instructions were given to return to the clinic in 48 to 72 hours

Outcomes

Non‐adherence to return visit for Mantoux test reading

Notes

Location: USA

Baseline data: comparable

Krishnaswami 1981

Methods

Randomized controlled trial

Generation of allocation sequence: unclear

Allocation concealment: unclear

Blinding of outcome assessors: unclear

Blinding of providers and participants: not possible

Inclusion of randomized participants in the analysis: 150/170 (89%); 20 participants excluded from main analysis because of death (8), lost to follow up (6), chemotherapy change (3), or transfer to more accessible clinics (3)

Protection against contamination: unclear

Participants

Number: 170 randomized; 150 analysed

Inclusion criteria: patients with symptoms reporting at the Institute of Tuberculosis and Chest Diseases in Madras; with radiographic evidence of tuberculosis but negative smears; aged ≥12 years; prescribed national tuberculosis programme recommended regimen; living within a radius of about 5 km from the clinic; bona fide residents of Madras city and regarded as stable (expected to remain in the city for at least 1 year)

Exclusion criteria: not stated

Interventions

Intervention
1. In the event of default, a health visitor went to the participant's home on the 4th day to persuade the patient to attend the clinic. If necessary, further visits were made on the 11th day, and at 1 and 2 months. At one of the latter 2 visits, a doctor accompanied the health visitor if the latter had met the patient at an early visit but had failed to persuade the patient to attend

Control
2. In the event of default, a reminder letter in Tamil (the local language) asking the patient to attend the clinic was posted to the home address on the evening of the 4th day. If the patient still failed to attend, a health visitor went to the home on the 11th day to see the patient personally and persuade him/her to attend

Outcomes

1. Failure to retrieve the defaulters with the first action for the first episode of default
2. Failure to retrieve the defaulters with the first action for all episodes of default
3. Mean number of drug collections for one year
4. Patients who discontinued treatment prematurely
5. Number of episodes of default

Notes

Location: South India

Baseline data: comparable

Default: defined by the trial authors as failure of the patient to collect his/her supply of drugs on the due date or within the next 3 days

Mohan 2003

Methods

Randomized controlled trial

Generation of allocation sequence: random‐numbers table

Allocation concealment: sequentially numbered and sealed opaque envelopes

Blinding of outcome assessors: yes

Blinding of providers and participants: not possible

Inclusion of randomized participants in the analysis: 480/480 (100%)

Protection against contamination: done

Participants

Number: 480 randomized

Inclusion criteria: new smear‐positive pulmonary tuberculosis (PTB); never been treated previously; delayed coming to collect drugs at the health centre for at least 3 days after scheduled appointment; identified from official patient record cards

Exclusion criteria: re‐treatment patients

Interventions

Intervention
1. Home visit by a local female volunteer from a local nongovernmental organization who was trained to motivate patient to attend health centre daily and to give health education (co‐intervention) for the patient and his/her family

Control
2. No home visit

Outcomes

1. Patient who did not complete treatment
2. Treatment interrupted for ≥ 2 consecutive months
3. Treatment failure: patient who is sputum positive at 5 months or later during treatment
4. Death
5. Sputum smear positive follow up

Notes

Location: Iraq

Baseline data: not reported

Default: defined by the author as treatment interrupted for ≥ 2 consecutive months

Paramasivan 1993

Methods

Randomized controlled trial

Generation of allocation sequence: random‐numbers table

Allocation concealment: centralized randomization by a third party

Blinding of outcome assessors: no

Blinding of providers and participants: no

Inclusion of randomized participants in the analysis: 200/200 (100%)

Protection against contamination: done

Participants

Number: 200 randomized

Inclusion criteria: newly diagnosed adult pulmonary tuberculosis patients; sputum positive for acid‐fast bacilli (AFB); no treatment or < 15 days previous treatment; not in moribund condition or suffering from disorders like diabetes, cardiac failure, or renal failure; willing to stay in the hospital for the initial 1‐month intensive phase of treatment

Exclusion criteria: not stated

Interventions

Intervention
1. First indirect defaulter action was posting of a reminder letter to the correct home address on the 4th day of the due date. The second defaulter action became due only when the first action failed to retrieve the patient, and it would be posted on the 8th day after the first action.

Control
2. No reminder letter

Outcomes

1. Number of patients who did not complete treatment
2. Number of patients who did not complete the treatment in spite of defaulter retrieval
3. Defaulters retrieval

Notes

Location: South India

Baseline data: not reported

Defaulter defined by author as a patient who failed to collect the drugs within 3 days after the due date of drug collection

Roberts 1983i

Methods

Randomized controlled trial

Generation of allocation sequence: unclear

Allocation concealment: unclear

Blinding of outcome assessors: unclear

Blinding of providers and participants: not possible

Inclusion of all randomized participants in the analysis: 200/200 (100%)

Protection against contamination: unclear

Participants

Number: 200 randomized

Inclusion criteria: volunteers who participated in a university‐sponsored tuberculosis detection drive; mostly college students

Exclusion criteria: not stated

Interventions

Intervention
1. Take‐home card
2. Postcard
3. Telephone call

Control
Direct person‐to‐person reminder

Outcomes

Number of participants who fail to return for skin‐test reading

Notes

Location: USA

Baseline data: comparable

Roberts 1983ii

Methods

Randomized controlled trial

Generation of allocation sequence: unclear

Allocation concealment: unclear

Blinding of outcome assessors: unclear

Blinding of providers and participants: not possible

Inclusion of all randomized participants in the analysis: 553/553 (100%)

Contamination: unclear

Participants

Number: 553 randomized

Inclusion criteria: volunteers who participated in a university‐sponsored tuberculosis detection drive

Exclusion criteria: not stated

Interventions

Intervention
1. Take‐home card with or without enhanced message on the importance of returning, and with or without three types of overt commitment to return

Control
2. No reminder card

Outcomes

Number of participants who fail to return for skin‐test reading

Notes

Location: USA

Baseline data: comparable

Sanmarti 1993

Methods

Randomized controlled trial

Generation of allocation sequence: unclear

Allocation concealment: unclear

Blinding of outcome assessors: unclear

Blinding of providers and participants: not possible

Inclusion of randomized participants in the analysis: 275/318 (85%); 43/318 (13.5%) withdrew from treatment

Protection against contamination: unclear

Participants

Number: 318 randomized

Inclusion criteria: school children of both sexes in the first year of primary school in state‐run and private schools in the provinces of Barcelona, on anti‐tuberculosis chemoprophylaxis

Exclusion criteria: children with active tuberculosis confirmed by medical examination and chest x‐ray

Interventions

Intervention of interest
1. Childrens' mothers were telephoned by a specialized nursing personnel every 3 months who informed them of the advantages of chemoprophylaxis for their child's health and encouraged them to continue with this preventive measure

Other interventions
2. Specialized nurse went to the patient's home every 3 months providing health education to the mother and child, encouraging them to continue with the preventive therapy, and giving them the same information leaflets given at the first visit
3. Child was seen by the physician every 3 months at the TB Prevention and Control Centre, providing health education and leaflets at each visit

Control
4. No health education activity performed

Outcomes

1. Non‐adherence to final appointment
2. Negative Eidus‐Hamilton reaction

Notes

Location: Spain

Baseline data: not reported

Tanke 1994

Methods

Quasi‐randomized controlled trial

Generation of allocation sequence: within each 5‐week period each message variation was used once on each weekday, different variations were used each day of a given week by a computer‐generated system

Allocation concealment: unclear

Blinding of outcome assessors: unclear

Blinding of providers and participants: not possible

Inclusion of randomized participants in the analysis: 2008/2008 (100%)

Protection against contamination: unclear

Participants

Number: 2008 randomized

Inclusion criteria: patients with scheduled appointments in the Tuberculosis Control Program of Santa Clara County Health Department over a period of 6 months

Exclusion criteria: not stated

Interventions

Interventions
1. Basic reminder: pre‐recorded message (TeleMinder system) from the county health department; identified the patient by name, indicated that the patient had an appointment the following day, and gave the address and phone number of the clinic twice; message could be repeated by remaining on the line; message did not refer to tuberculosis
2. Basic reminder plus authority endorsement: identified the Public Health Nurse at the Health Department as the source of the message
3. Basic reminder plus importance statement: following statement was inserted after the basic information: "Coming to this appointment is important so that you and your family will not become seriously ill."
4. Basic reminder plus importance statement plus authority endorsement

Control
5. No message

Appropriate recorded message was sent to patients between 1800 and 2100 the evening before the scheduled appointment. The system allows a message to be left on answering machines and to call back up to 5 times at half‐hour intervals if patients' lines were busy or there was no answer after 8 rings. For households whose primary language was English, Spanish, Vietnamese, or Tagalog, the message was sent in that language

Outcomes

Non‐attendance for a scheduled appointment: if a patient had > 1 appointment during the course of the study, only data from the first appointment were included

Notes

Location: USA

Baseline data: not reported

Tanke 1994: diagnosis arm

Methods

Tanke 1994 results for patients in the Reactor Clinic for diagnosis

Participants

Interventions

Outcomes

Notes

Tanke 1994: prophylaxis arm

Methods

Tanke 1994 results for patients in the INH [isoniazid] Clinic for prophylaxis

Participants

Interventions

Outcomes

Notes

Tanke 1994: treatment arm

Methods

Tanke 1994 results for patients in the Case Clinic for treatment

Participants

Interventions

Outcomes

Notes

Tanke 1997

Methods

Randomized controlled trial

Generation of allocation sequence: unclear

Allocation concealment: unclear

Blinding of outcome assessors: unclear

Blinding of providers and participants: not possible

Inclusion of randomized participants in the analysis: 701/701 (100%)

Protection against contamination: unclear

Participants

Number: 701 randomized

Inclusion criteria: persons undergoing tuberculin skin test at the 2 largest clinics of Santa Clara (California) County Immunization Program

Exclusion criteria: not stated

Interventions

Intervention
1. Pre‐recorded telephone reminder message (TeleMinder system) between 1800 and 2100 the evening before the day on which they were to return to have their skin test read, and the information was repeated twice in the participant's primary language

Control
2. No reminder message

Outcomes

1. Total return failures
1.1. 2‐day delay
1.2. 3‐day delay

Notes

Location: USA

Baseline data: Not reported

Characteristics of excluded studies [ordered by study ID]

Study

Reason for exclusion

AL‐Hajjaj 2000

Case‐control study design

Alcaide Megías 1990

Intervention did not include reminders or late patient tracers

Bordley 2001

Most participants did not have need for screening, prophylaxis, or treatment for tuberculosis, and results for the individuals in these categories were not presented separately

Gordillo 2003

Intervention did not include reminders or late patient tracers

Hovell 2003

Intervention did not include reminders or late patient tracers

Jin 1993

Intervention did not include reminders or late patient tracers

Krishna 2002

Review article

Lin 2006

Cohort study design

Morisky 1990

Intervention did not include reminders or late patient tracers, except for those routinely provided and also applied to the control group

Morisky 2001

Intervention did not include reminders or late patient tracers

Nyamathi 2007

Process of late patient tracers not described, and the main objective was to assess predictors of latent tuberculosis infection completion by using structural equation modelling among homeless adults

Thiam 2007

Reminders or late patient tracers not adequately described or systematically applied

Data and analyses

Open in table viewer
Comparison 1. Late patient tracers vs no late patient tracer

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Patients who did not complete treatment Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 1.1

Comparison 1 Late patient tracers vs no late patient tracer, Outcome 1 Patients who did not complete treatment.

Comparison 1 Late patient tracers vs no late patient tracer, Outcome 1 Patients who did not complete treatment.

1.1 Home visit plus health education vs usual care (directly observed therapy, short‐course)

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 Reminder letter vs usual care

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Failure of patients to return to treatment after first missed appointment Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 1.2

Comparison 1 Late patient tracers vs no late patient tracer, Outcome 2 Failure of patients to return to treatment after first missed appointment.

Comparison 1 Late patient tracers vs no late patient tracer, Outcome 2 Failure of patients to return to treatment after first missed appointment.

Open in table viewer
Comparison 2. Late patient tracers (home visit plus health education) vs usual care

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Patients who did not complete treatment Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 2.1

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 1 Patients who did not complete treatment.

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 1 Patients who did not complete treatment.

2 Treatment interrupted for 2 consecutive months or more Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 2.2

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 2 Treatment interrupted for 2 consecutive months or more.

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 2 Treatment interrupted for 2 consecutive months or more.

3 Treatment failure Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 2.3

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 3 Treatment failure.

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 3 Treatment failure.

4 Death Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 2.4

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 4 Death.

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 4 Death.

5 Sputum‐smear positive follow up Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 2.5

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 5 Sputum‐smear positive follow up.

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 5 Sputum‐smear positive follow up.

5.1 2 months

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.2 5 months

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.3 End of treatment

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Open in table viewer
Comparison 3. Late patient tracers (home visit) vs letter

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Patients who did not complete treatment Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 3.1

Comparison 3 Late patient tracers (home visit) vs letter, Outcome 1 Patients who did not complete treatment.

Comparison 3 Late patient tracers (home visit) vs letter, Outcome 1 Patients who did not complete treatment.

2 Failure of patients to return for treatment after missed appointment Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 3.2

Comparison 3 Late patient tracers (home visit) vs letter, Outcome 2 Failure of patients to return for treatment after missed appointment.

Comparison 3 Late patient tracers (home visit) vs letter, Outcome 2 Failure of patients to return for treatment after missed appointment.

Open in table viewer
Comparison 4. Reminders (automated telephone message) vs no message

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Non‐attendance at clinic appointment Show forest plot

3

Risk Ratio (M‐H, Random, 95% CI)

Totals not selected

Analysis 4.1

Comparison 4 Reminders (automated telephone message) vs no message, Outcome 1 Non‐attendance at clinic appointment.

Comparison 4 Reminders (automated telephone message) vs no message, Outcome 1 Non‐attendance at clinic appointment.

1.1 Basic message vs no message

3

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

1.2 Message + authority vs no message

3

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

1.3 Message + importance statement vs no message

3

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

1.4 Message + authority + importance vs no message

3

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

1.5 Any type of message vs no message

3

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

Open in table viewer
Comparison 5. Reminders (non‐automated reminder phone call) vs no reminder

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Non‐adherence to Mantoux test reading Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 5.1

Comparison 5 Reminders (non‐automated reminder phone call) vs no reminder, Outcome 1 Non‐adherence to Mantoux test reading.

Comparison 5 Reminders (non‐automated reminder phone call) vs no reminder, Outcome 1 Non‐adherence to Mantoux test reading.

1.1 Reminder phone call vs no call

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Open in table viewer
Comparison 6. Reminder plus health education vs usual care

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Non‐adherence to final clinic appointment Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 6.1

Comparison 6 Reminder plus health education vs usual care, Outcome 1 Non‐adherence to final clinic appointment.

Comparison 6 Reminder plus health education vs usual care, Outcome 1 Non‐adherence to final clinic appointment.

1.1 Phone call plus health education vs usual care

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 Home visit plus health education vs usual care

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Open in table viewer
Comparison 7. Reminder vs other types of reminders and no reminder

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Failed to return for skin test reading Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 7.1

Comparison 7 Reminder vs other types of reminders and no reminder, Outcome 1 Failed to return for skin test reading.

Comparison 7 Reminder vs other types of reminders and no reminder, Outcome 1 Failed to return for skin test reading.

1.1 Expert vs non‐expert

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 Take‐home card vs postcard

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.3 Take‐home card vs telephone call

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.4 Take‐home card vs person‐to‐person

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.5 Postcard vs telephone call

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.6 Postcard vs person‐to‐person

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.7 Telephone call vs person‐to‐person

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Failed to return for skin test reading Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Analysis 7.2

Comparison 7 Reminder vs other types of reminders and no reminder, Outcome 2 Failed to return for skin test reading.

Comparison 7 Reminder vs other types of reminders and no reminder, Outcome 2 Failed to return for skin test reading.

Late patient tracers vs no late patient tracer: Patients who did not complete treatment
Figuras y tablas -
Figure 1

Late patient tracers vs no late patient tracer: Patients who did not complete treatment

Late patient tracers (home visit) vs letter: Patients who did not complete treatment
Figuras y tablas -
Figure 2

Late patient tracers (home visit) vs letter: Patients who did not complete treatment

Reminders (automated telephone message) vs no message: Non‐attendance at clinic appointment
Figuras y tablas -
Figure 3

Reminders (automated telephone message) vs no message: Non‐attendance at clinic appointment

Reminder plus health education vs usual care: Non‐adherence to final clinic appointment
Figuras y tablas -
Figure 4

Reminder plus health education vs usual care: Non‐adherence to final clinic appointment

Comparison 1 Late patient tracers vs no late patient tracer, Outcome 1 Patients who did not complete treatment.
Figuras y tablas -
Analysis 1.1

Comparison 1 Late patient tracers vs no late patient tracer, Outcome 1 Patients who did not complete treatment.

Comparison 1 Late patient tracers vs no late patient tracer, Outcome 2 Failure of patients to return to treatment after first missed appointment.
Figuras y tablas -
Analysis 1.2

Comparison 1 Late patient tracers vs no late patient tracer, Outcome 2 Failure of patients to return to treatment after first missed appointment.

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 1 Patients who did not complete treatment.
Figuras y tablas -
Analysis 2.1

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 1 Patients who did not complete treatment.

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 2 Treatment interrupted for 2 consecutive months or more.
Figuras y tablas -
Analysis 2.2

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 2 Treatment interrupted for 2 consecutive months or more.

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 3 Treatment failure.
Figuras y tablas -
Analysis 2.3

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 3 Treatment failure.

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 4 Death.
Figuras y tablas -
Analysis 2.4

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 4 Death.

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 5 Sputum‐smear positive follow up.
Figuras y tablas -
Analysis 2.5

Comparison 2 Late patient tracers (home visit plus health education) vs usual care, Outcome 5 Sputum‐smear positive follow up.

Comparison 3 Late patient tracers (home visit) vs letter, Outcome 1 Patients who did not complete treatment.
Figuras y tablas -
Analysis 3.1

Comparison 3 Late patient tracers (home visit) vs letter, Outcome 1 Patients who did not complete treatment.

Comparison 3 Late patient tracers (home visit) vs letter, Outcome 2 Failure of patients to return for treatment after missed appointment.
Figuras y tablas -
Analysis 3.2

Comparison 3 Late patient tracers (home visit) vs letter, Outcome 2 Failure of patients to return for treatment after missed appointment.

Comparison 4 Reminders (automated telephone message) vs no message, Outcome 1 Non‐attendance at clinic appointment.
Figuras y tablas -
Analysis 4.1

Comparison 4 Reminders (automated telephone message) vs no message, Outcome 1 Non‐attendance at clinic appointment.

Comparison 5 Reminders (non‐automated reminder phone call) vs no reminder, Outcome 1 Non‐adherence to Mantoux test reading.
Figuras y tablas -
Analysis 5.1

Comparison 5 Reminders (non‐automated reminder phone call) vs no reminder, Outcome 1 Non‐adherence to Mantoux test reading.

Comparison 6 Reminder plus health education vs usual care, Outcome 1 Non‐adherence to final clinic appointment.
Figuras y tablas -
Analysis 6.1

Comparison 6 Reminder plus health education vs usual care, Outcome 1 Non‐adherence to final clinic appointment.

Comparison 7 Reminder vs other types of reminders and no reminder, Outcome 1 Failed to return for skin test reading.
Figuras y tablas -
Analysis 7.1

Comparison 7 Reminder vs other types of reminders and no reminder, Outcome 1 Failed to return for skin test reading.

Comparison 7 Reminder vs other types of reminders and no reminder, Outcome 2 Failed to return for skin test reading.
Figuras y tablas -
Analysis 7.2

Comparison 7 Reminder vs other types of reminders and no reminder, Outcome 2 Failed to return for skin test reading.

Table 1. Detailed search strategies

Search set

Cochrane SRa

CENTRAL

MEDLINEb

EMBASEb

LILACSb

SCI‐EXPANDED & SSCI

CINAHL

1

tuberculosis

tuberculosis

tuberculosis

tuberculosis

tuberculosis

tuberculosis

tuberculosis

2

adherence

PATIENT COMPLIANCE

TUBERCULOSIS/DRUG THERAPY/PREVENTION AND CONTROL

TUBERCULOSIS

adherence

adherence

adherence

3

compliance

PATIENT DROPOUTS

PATIENT COMPLIANCE

PATIENT‐COMPLIANCE

compliance

compliance

compliance

4

monitor*

REMINDER SYSTEMS

PATIENT DROPOUTS

medication adherence

monitor*

monitor*

monitor*

5

reminder*

TREATMENT REFUSAL

COOPERATIVE BEHAVIOUR

REMINDER‐SYSTEM

reminder*

reminder*

reminder*

6

2 or 3 or 4 or 5 or 6

DIRECTLY OBSERVED THERAPY

TREATMENT REFUSAL

TREATMENT‐REFUSAL

2 or 3 or 4 or 5

non‐adherence

non‐adherence

7

1 and 6

medication adherence

medication adherence

DIRECTLY‐OBSERVED‐THERAPY

1 and 6

late patient tracer

late patient tracer

8

electronic monitoring

REMINDER SYSTEMS

electronic monitoring

2‐7/or

2‐7/or

9

nonadherence

electronic monitoring

nonadherence

1 and 8

1 and 8

10

non‐adherence

nonadherence

non‐adherence

11

late patient tracer

non‐adherence

late patient tracer

12

2‐11/or

DIRECTLY OBSERVED THERAPY

1 or 2

13

1 and 12

late patient tracer

3‐11/or

14

1 or 2

13 and 14

15

3‐13/or

16

14 and 15

aCochrane Infectious Diseases Group Specialized Register and the Cochrane Effective Practice and Organisation of Care Group Specialized Register.
bSearch terms used in combination with the search strategy for retrieving trials developed by The Cochrane Collaboration (Lefebvre 2006); upper case: MeSH or EMTREE heading; lower case: free text term.

Figuras y tablas -
Table 1. Detailed search strategies
Table 2. Risk of bias assessment

Intervention

Trial

Design

Generation of allocation sequence

Allocation concealment

Blinded assessment

Inclusion of randomized participants in the analysis

Protection against contamination

Late patient tracers

Krishnaswami 1981

RCT

Unclear

Unclear

Unclear

Adequate

Unclear

Paramasivan 1993

RCT

Adequate

Adequate

No

Adequate

Done

Mohan 2003

RCT

Adequate

Adequate

Yes

Adequate

Done

Reminder systems

Roberts 1983i

RCT

Unclear

Unclear

Unclear

Adequate

Unclear

Roberts 1983ii

RCT

Unclear

Unclear

Unclear

Adequate

Unclear

Sanmarti 1993

RCT

Unclear

Unclear

Unclear

Adequate

Unclear

Tanke 1994

Quasi‐RCT

Inadequate

Unclear

Unclear

Adequate

Unclear

Cheng 1997

Quasi‐RCT

Inadequate

Unclear

Unclear

Adequate

Unclear

Tanke 1997

RCT

Unclear

Unclear

Unclear

Adequate

Unclear

RCT: randomized controlled trial.

Figuras y tablas -
Table 2. Risk of bias assessment
Comparison 1. Late patient tracers vs no late patient tracer

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Patients who did not complete treatment Show forest plot

2

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

1.1 Home visit plus health education vs usual care (directly observed therapy, short‐course)

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 Reminder letter vs usual care

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Failure of patients to return to treatment after first missed appointment Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Figuras y tablas -
Comparison 1. Late patient tracers vs no late patient tracer
Comparison 2. Late patient tracers (home visit plus health education) vs usual care

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Patients who did not complete treatment Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

2 Treatment interrupted for 2 consecutive months or more Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

3 Treatment failure Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

4 Death Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

5 Sputum‐smear positive follow up Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

5.1 2 months

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.2 5 months

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5.3 End of treatment

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Figuras y tablas -
Comparison 2. Late patient tracers (home visit plus health education) vs usual care
Comparison 3. Late patient tracers (home visit) vs letter

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Patients who did not complete treatment Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

2 Failure of patients to return for treatment after missed appointment Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Figuras y tablas -
Comparison 3. Late patient tracers (home visit) vs letter
Comparison 4. Reminders (automated telephone message) vs no message

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Non‐attendance at clinic appointment Show forest plot

3

Risk Ratio (M‐H, Random, 95% CI)

Totals not selected

1.1 Basic message vs no message

3

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

1.2 Message + authority vs no message

3

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

1.3 Message + importance statement vs no message

3

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

1.4 Message + authority + importance vs no message

3

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

1.5 Any type of message vs no message

3

Risk Ratio (M‐H, Random, 95% CI)

0.0 [0.0, 0.0]

Figuras y tablas -
Comparison 4. Reminders (automated telephone message) vs no message
Comparison 5. Reminders (non‐automated reminder phone call) vs no reminder

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Non‐adherence to Mantoux test reading Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

1.1 Reminder phone call vs no call

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Figuras y tablas -
Comparison 5. Reminders (non‐automated reminder phone call) vs no reminder
Comparison 6. Reminder plus health education vs usual care

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Non‐adherence to final clinic appointment Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

1.1 Phone call plus health education vs usual care

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 Home visit plus health education vs usual care

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

Figuras y tablas -
Comparison 6. Reminder plus health education vs usual care
Comparison 7. Reminder vs other types of reminders and no reminder

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Failed to return for skin test reading Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

1.1 Expert vs non‐expert

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 Take‐home card vs postcard

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.3 Take‐home card vs telephone call

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.4 Take‐home card vs person‐to‐person

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.5 Postcard vs telephone call

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.6 Postcard vs person‐to‐person

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

1.7 Telephone call vs person‐to‐person

1

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Failed to return for skin test reading Show forest plot

1

Risk Ratio (M‐H, Fixed, 95% CI)

Totals not selected

Figuras y tablas -
Comparison 7. Reminder vs other types of reminders and no reminder