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Table 1 Economic evaluations of latent tuberculosis infection screenings published up to July 2014

From: A scoping review of cost-effectiveness of screening and treatment for latent tuberculosis infection in migrants from high-incidence countries

Author (Country; Year)

Alternatives

Data source

EE Type

Perspective

Model Horizon Discount rate

Cost

Cost description

Differential Costs

ICER

Conclusion

Dasgupta et al. (Canada; 2000) [19]

1. Screening (medical evaluation, CXR);

Administrative data bases

CEA

Health care payer

Markov 20 years

Direct

CXR, clinic visits, investigations, hospitalization, drugs, physicians’ and pharmacists’ fees, administrative activities.

• TB case detected: CAN$ 31,418; prevented: CAN$ 73,125;

 

Close-contact investigation was highly cost-effective and resulted in net savings. Immigrant applicant screening and surveillance programs had a significant impact but were much less cost-effective, in large part because of substantial operational problems. Radiographic screening of newly arriving foreign-born populations for TB could be cost-effective and have considerable individual and public health benefits.

• CAN$ 55,728; CAN$ 155,729;

2. Surveillance of inactive TB, including LTBI treatment;

• CAN$ 10,275; CAN$ 29,668.

3. Close-contact investigation

Khan et al. (USA; 2002) [18]

1. No LTBI screening;

Data bases

CEA, CUA

Societal

Markov Lifetime 3.00%

Health Direct

Transportation, ambulatory care, services of interpreters, laboratory tests, medications, adverse drug reactions, hospitalization, and patients’ time.

Total savings: US$60 to US$90 million, assuming to avert 9–10 thousand TB infections per year.

CEA

Results variable according to country of origin.

• TST followed by INH: savings or dominated, depending on regions.

2. TST followed by INH;

Indirect

A strategy of detecting and treating LTBI was cost-saving among immigrants from Mexico, Haiti, sub-Saharan Africa, South Asia, and developing nations in East Asia and the Pacific.

• TST followed RIF: dominant.

4. TST followed by RIF plus PZM.

• TST followed RIF plus PZM: saving or cost/effective (US$2,551 - US$149,978 per future case averted), depending on regions.

3. TST followed by RIF;

per QALY

Screening was highly cost-effective among immigrants from other developing nations. RIF-PZM was the preferred treatment for treating LTBI in immigrants from Vietnam, Haiti, and the Philippines.

• TST followed by INH: savings, US$914 - US$5,952, or dominated depending on regions.

• TST followed by RIF: dominant.

• TST followed by RIF plus PZM: savings, or US$1,276 - US$53,388, depending on regions.

Brassard et al. (Canada; 2006) [17]

1. LTBI school-screening program in newly arrived immigrant children (TST followed by INH);

Clinical trialc

CBA

Health care payer

No

Health Direct

Total material and labor costs associated with the school-screening program and the associate investigations for children and associates.

Total savings: CAN$ 363,923.

 

The school-based LTBI-screening program was found to be cost-effective.

Without associate investigation: CAN$ 268,393.

Savings were mainly due to hospitalization costs.

2. Active TB management through passive case finding.

Porco et al. (USA; 2006) [20]

1. Follow-up of TB-notification patients, including LTBI treatment for latently infected individuals;

Published literature, administrative data bases

CEA, CUA

Health care payer

Markov 20 years 3.00%

Direct

Diagnostic tests, nursing assessments and doctor visits, drugs, side effects, hospitalizations.

The program yielded 7.7 net QALYs, US$ 25,000 in net savings, and prevented 4 cases of TB.

Treatment of TB4s was cost-saving.

Domestic follow up is highly cost-effective as early detection and treatment reduces the rate of hospitalization.

Treatment of TB2s was highly cost-effective: US$4,400 per QALY and US$4,700 per case prevented.

2. No follow-up.

Oxlade O et al. (Canada;2007) [11]

1. CXR;

Published literature, administrative data bases

CEA

Societal

Markov

Health Direct

All government and health system costs, patients’ out-of-pocket expenditures, but not TB-related death or disability.

Savings only in high-very high risk populations:

CXR - the least costly ICER per case prevented: CAN$ 875 for immigrants from high-incidence TB up to CAN$ 2.2 million from low incidence.

Screening with CXR would be the most and QFT the least cost-effective.

2. TST;

20 years

3. QFT;

3.00%

4. TST+QTF;

• CXR - CAN$ 44,710; CAN$ 65,490;

Screening for LTBI, with TST or QFT, is cost-effective only if the risk of disease is high. The most cost-effective use of QFT is to test TST-positive persons.

5. No screening.

QFT - the most expensive: CAN$62,643 up to CAN$1,122,200.

• TST - CAN$ 136260; CAN$ 476320;

TST - better than QFT with saving up to CAN$35,000 compared to QFT, but in populations BCG-vaccinated after infancy, where TST more expensive because of low specificity.

Three scenarios:

• QFT - CAN$ 100,490; CAN$ 440,550.

Screening with TST or QFT was much more cost-effective in contacts than entering immigrants.

a) immigration entry screening;

However, the selection of screening strategy is less important than program performance. Programs considering these new ex vivo tests for LTBI should thus first ensure that a high proportion of those with positive tests will be medically evaluated, prescribed and complete therapy.

b) close or

c) casual contacts.

Hardy et al. (UK; 2010) [21]

1. NICE guidance 2006;

Clinical trialc

CEA

Health care payer

No

Health Direct

Cost per case LTBI identified

Cost per case identified:

 

QFT-first protocol can be carried out more cheaply than a CXR-first protocol, with a cost-saving of about 35% (£67.65) compared to NICE protocol. This saving is due to the reduced number of CXRs required.

• NICE protocol: £160.81;

• Leed protocol: £93.16.

2. Leeds protocol: QTF first in immigrants from countries with TB incidence >200/105 followed by CXR (all ages, but mean age was 30.8 year).

Linas et al. (USA; 2011) [23]

1. TST;

Published literature

CEA, CUA

Health care payer

Markov Lifetime 3.00%

Health Direct

Nursing and physician visits, diagnostic tests, medications, hospitalizations, contact tracing, and directly observed therapy.

 

• Individuals at highest risk of TB reactivation (close contacts and HIV-infected) - ICER of IGRA compared to TST was <$100,000/QALY gained.

In foreign-born subjects IGRA was cost-saving compared to TST and cost-effective compared to no screening.

2. IGRA;

3. No LTBI screening.

Risk-groupsa

• The foreign-born - IGRA was cost-saving compared to TST and cost-effective compared to no screening (ICER <$100,000/ QALY gained).

• Vulnerable populations (homeless, drug user, former prisoner) - ICER of TST screening was approximately $100,000-$150,000/QALY gained, but IGRA was not cost-effective.

• Medical co-morbidities (diabetes and others) - ICER of screening with TST or IGRA was >$100,000/QALY.

Pareek et al. (UK; 2011) [15]

1. QFT;

Clinical trialc

CEA

Government health care payer

Markov 20 years 3.50%

Direct

UK NICE TB guidelines

Screening of immigrants from any countries irrespective of tuberculosis incidence would cost:

• Screen immigrants aged 16–35 years from countries with incidences/105

Screening for latent infection can be implemented cost-effectively at a level of incidence that identifies most immigrants with latent tuberculosis, thereby preventing substantial numbers of future cases of active tuberculosis.

2. NICE guidance 2006b.

• QFT more than £1.5 million and prevent 44.5 cases of tuberculosis;

≥250/105: £ 17,956 per case averted; ≥ 150/105: £ 20,819; ≥40/105: £ 29,403.

Screen immigrants aged ≤35 years irrespective of TB incidence: £ 101,938.

• NICE guidance ≈£850,000 and prevent 13.2 cases.

Pareek et al. (UK; 2012) [16]

1. TST+ in <35y old immigrants;

Clinical trialc

CEA

Government health care payer

Markov 20 years

Direct

 

Current UK national guidance associated with additional costs of between £594,957 and £1,530,303 over 20 years.

• QFN (single): £21,565 - £34,754 per TB case averted.

Mandatory CXR on arrival could be safely eliminated in order to improve screening cost-effectiveness with single-step QTF at incidence threshold >250/105 per year.

• CXR plus single QFN: £59,489.

2. QTF+ in <35y old immigrants;

• CXR plus single T.SPOT.TB: £402,422.

3. T-SPOT+ in <35y old immigrants.

All with or without CXR port of entry.

Iqbal et al. (USA, 2014) [22]

1. QFT;

Administrative data base (2007)

CEA

Government health care payer

Decision model

Health Direct

Screening, CXR, Treatments, lab tests and diagnostics, physicians’ and staff time.

Total screening cost: TST US$38; QFT-G US$74

Differential costs for screening and follow-up for subjects who were estimated to be test positive on 1,000 latent TB infections

QFT is cost-effective especially for high-risk populations such as foreign-born individuals.

2. TST.

Key assumption.

False positive rates:

• U.S. born

• U.S. born

QFT: +US$25,037 vs. TST.

TST 66%; QFT 40%

• Foreign born

Treatment duration: 9 months

QFT: −US$135,946.

• Foreign born

TST 69%; QFT 18%

Treatment duration: 9 months

  1. EE economic evaluation, ICER Incremental cost-effectiveness ratio, CEA cost-effectiveness analysis, CXR chest X-ray, CAN$ Canadian dollar, INH isoniazid, RIF rifampicin, PZM pyrazinamide, CUA cost-utility analysis, US$ United States dollar, TST tuberculin skin test, QTF Quantiferon, QALY Quality Adjusted Life Years, CBA cost-benefit analysis, LTBI latent tuberculosis infection, TB tuberculosis, NICE National Institute for Health and Care Excellence, TB2 subjects with evidence of infection but no evidence of disease, TB4 subjects with stable radiographic abnormalities suggestive of TB together with evidence of TB infection and negative bacteriologic studies
  2. a) Risk groups including recent immigrant adults and children, foreign-born residents living in the U.S. for more than five years (stratified by age), close contact adults and children, HIV-infected individuals, the homeless, injection drug users, former prisoners, gastrectomy patients, underweight patients, and persons with silicosis, diabetes, and end-stage renal disease.
  3. b) CXR in all immigrants from countries with TB incidence>40/105 and >16yo; TST if <16yo or <35yo from Sub Saharan Africa or from countries >500/105; QTF in TST positive to confirm LTBI.
  4. c) Clinical trial description reported as Additional file 1: Table S2