· Technology
for TB Control: While the technology to control TB exists, it is generally
underused.
· DOTS
(Directly Observed Treatment, Short-course):
- Originally referred to
directly observed treatment with short-course chemotherapy.
- Now a broader public
health strategy with five key elements:
- Political
commitment.
- Case
detection through sputum smear microscopy,
mostly among self-referring, symptomatic patients.
- Standard
short-course chemotherapy with supportive
patient management, including DOT.
- Reliable
drug supply system.
- Standardized
recording and reporting system,
including treatment outcome evaluations.
· MDG Framework
for TB Control:
- Comprises two
DOTS-focused measures:
- Case
detection.
- Treatment
success.
- Includes three impact
measures applicable to TB control in general:
- Incidence.
- Prevalence.
- Deaths.
- Promotes
epidemiological evaluation beyond DOTS and a comprehensive TB control
approach.
· Comprehensive
Approach Beyond DOTS:
- Prevention
methods and improved patient care.
- Engaging public and
private clinicians, especially for patients with HIV or drug-resistant TB.
- Integration
of new technologies and optimization of
existing tools.
· Estimating
TB Incidence Rates:
- Rarely measured
directly; often estimated from:
- Population-based
surveys on M. tuberculosis infection or TB disease prevalence.
- Independent,
qualitative assessments of surveillance systems.
- Accuracy limitations
due to challenges in calculating incidence from prevalence.
· Regional
TB Management Challenges:
- Africa and Eastern
Europe face TB control challenges linked to HIV/AIDS and drug
resistance.
- Region-specific
solutions are needed for these unique problems.
· DOTS
Limitations and Expansion:
- By 2003, DOTS had
nearly maxed out the utility of public notification systems.
- Next steps involve:
- Adapting
DOTS for non-public healthcare facilities
(e.g., in Indonesia).
- Encouraging
all medical practitioners to adopt the basic DOTS care package.
- Expanding
health services to areas lacking professional healthcare.
· Factors
Influencing TB Incidence and Death Rates:
- Not solely determined
by drug treatment; other factors include:
- Nutritional
status, tobacco and alcohol use.
- Other
infections and genetic susceptibility.
- These determinants
warrant further study to fully understand TB dynamics.
· TB Death
Statistics:
- Ideally sourced from
reliable vital registration systems.
- Many poorer countries
lack systematic or accurate cause-of-death records.
Dye, C., Watt, C.J., Bleed, D.M., Hosseini, S.M. and Raviglione, M.C., 2005. Evolution of tuberculosis control and prospects for reducing tuberculosis incidence, prevalence, and deaths globally. Jama, 293(22), pp.2767-2775.
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Liu, Q., You, N., Wen, J., Wang, J., Ge, Y., Shen, Y., Ding, X., Lu, P., Chen, C., Zhu, B. and Zhu, L., 2023. Yield and efficiency of a population-based mass tuberculosis screening intervention among persons with diabetes in Jiangsu Province, China. Clinical Infectious Diseases, 77(1), pp.103-111.
Feasibility and Focus: Mass tuberculosis (TB) screening among persons with diabetes (PWD) is feasible but may not be cost-efficient due to low detection rates.
Cost Efficiency: The high costs were largely driven by diabetes management rather than TB-related expenses.
Targeted Screening: Concentrating screening efforts in populations with at least 100 TB cases per 100,000 persons is effective and should be continued.
Risk-Stratified Approaches: Risk-stratified screening could be more practical in settings with low to medium TB burden.
Symptom Screening Limitations: Relying solely on symptom screening is insufficient for TB detection, highlighting the need for more comprehensive methods.
Program Integration: Successful implementation required collaboration between diabetes and TB control programs, leveraging existing community-based diabetes screening efforts.
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Alisjahbana, B., Sahiratmadja, E., Nelwan, E.J., Purwa, A.M., Ahmad, Y., Ottenhoff, T.H., Nelwan, R.H., Parwati, I., Meer, J.W.V.D. and Crevel, R.V., 2007. The effect of type 2 diabetes mellitus on the presentation and treatment response of pulmonary tuberculosis. Clinical infectious diseases, 45(4), pp.428-435.
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