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Appendix III - Supplementary Tables

from 6 - Health Service Delivery

Published online by Cambridge University Press:  04 September 2021

Jo. M. Martins
Affiliation:
International Medical University, Malaysia
Indra Pathmanathan
Affiliation:
United Nations University - International Institute for Global Health
David T. Tan
Affiliation:
United Nations Development Programme
Shiang Cheng Lim
Affiliation:
RTI International
Pascale Allotey
Affiliation:
United Nations University - International Institute for Global Health

Summary

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2021
Creative Commons
Creative Common License - CCCreative Common License - BYCreative Common License - NCCreative Common License - SA
This content is Open Access and distributed under the terms of the Creative Commons Attribution licence CC-BY-NC-SA 4.0 https://creativecommons.org/cclicenses/

Appendix III Supplementary Tables

Supplementary Table 6.a Ten principal causes of admissions and deaths, 1960, 1974 and 1996

Causes1960, rank (%)1974, rank (%)1996, rank (%)
AdmissionsDeathsAdmissionsDeathsDeaths
Accidents1 (10.14)7 (5.63)1 (13.48)3 (10.53)3 (9.44)
Skin diseases2 (4.11)6 (2.58)
Gastroenteritis/digestive system diseases3 (3.90)3 (8.93)3 (3.71)8 (2.87)7 (4.60)
Complications of pregnancy4 (3.72)10 (2.64)2 (4.97)
Tuberculosis5 (2.88)5 (7.36)7 (4.40)
Malaria6 (2.65)
Mental illness7 (2.42)4 (3.10)
Bronchitis8 (2.34)10 (1.95)
Pyrexia of unknown origin9 (2.21)8 (2.16)
Heart diseases10 (1.77)2 (9.94)5 (2.59)2 (15.02)1 (15.61)
Disease of early infancy1 (15.2)7 (2.29)1 (18.99)6 (7.82)
Cardiovascular/cerebrovascular diseases8 (3.17)9 (2.08)4 (7.32)4 (9.27)
Pneumonia4 (8.48)6 (6.50)8 (4.17)
Neoplasms6 (6.03)5 (6.71)5 (8.92)
Deficiency diseases9 (2.81)10 (1.43)
Liver diseases9 (2.32)
Septicaemia2 (10.12)

Supplementary Table 6.b Infant and child mortality rates, 1957–2017

1957197019831990200020102016/2017
Infant mortality rate (per 1,000 live births)68.939.420.213.166.77.3
Neonatal mortality rate (per 1,000 live births)29.621.412.38.53.14.34.2
Toddler mortality rate (per 1,000 population aged 1–4 years)84.21.70.90.50.40.4
Under-5 mortality rate (per 1,000 live births)110.455.926.616.87.98.58.6

Supplementary Table 6.c National disease control programmes

Disease control programmeKey strategiesSupporting strategiesOutcomes
PreventionScreening/ detectionTreatment and managementHuman resource and capacity buildingSurveillance systemCommunity participation
Yaws Elimination Campaign, 1954 – with assistance from WHO and UNICEF (UN Children’s Fund)
  • Mass survey campaign, with annual re-surveys.

  • When the incidence rates declined, modified school surveys were deployed

  • every 6 months. If infectious cases were found, the entire area would be studied.

Mass treatment using procaine penicillin for open cases, latent cases and contact.Yaws elimination unit was set up.
  • Incidence rate declined from 140.85 per 100,000 population in 1958 to <2 in 1974.

  • Yaws control activities were integrated into the general health services in 1974. All health workers were trained to recognise yaws cases.

Filariasis Control Programme, 1960Case detection: House and population censuses and nocturnal mass blood survey. Whenever a nocturnal survey was not feasible, the diethylcarbamazine (DEC) stimulation technique was used during follow-up of cases or in school surveys.Mass treatment in the locality using DEC: Individual case follow-up was carried out after 3–5 months while the locality was resurveyed after about 2–3 years.
  • Peninsular Malaysia: Control team (medical assistant, public health auxiliary, junior laboratory technician, driver and vehicle).

  • Sabah and Sarawak: Ad hoc team to conduct surveys and treatment in specific areas.

  • 1988–90: There appeared to be a decreasing trend in the number of filariasis cases detected countrywide.

  • 1983: incorporated into the Vector-Borne Disease Control Programme.

  • National TB Control Programme, 1961 –

  • monitored and co-ordinated by the Division of TB and National TB Control Centre

  • National health education campaigns: To increase public awareness of TB signs and symptoms and early diagnosis.

  • BCG vaccination programme: Between 1961 and 1974, at least 75% of the susceptible population had been vaccinated (total BCG vaccinations performed: 4,965,982).

Case finding programme: Early case detection among symptomatic and high-risk groups (at least 66%) in the community using mass miniature radiography (MMR), X-ray, bacteriological and sputum examination and referred for appropriate treatment.
  • Treatment programme: 20-month standard treatment regimen (streptomycin with isoniazid or isoniazid with para-aminosalicylic acid or thiacetazone) for patients to render them non-infective (at least 95%).

  • The National TB Control Centre served as the national referral hospital for patients with complicated TB.

  • Countrywide training programme conducted by the National TB Centre, supported by hospitals, for different categories of personnel (doctors, nurses, hospital assistants, health inspectors, medical students and lab technicians).

  • Formation of State TB Control/Managerial Teams in 1973 to supervise and monitor the treatment programme and contact tracing.

1973: The TB registry was established.Working with MAPTB to provide socio-economic aid and increase community participation to reduce defaulter rates for treatment.
  • TB is no longer the major cause of death.

  • The National TB Control Programme was integrated with public health and general medical services in 1995.

Malaria Eradication Programme, 1967–82: Part of the Global Malaria Eradication Programme

Vector control:

Residual insecticide spraying using DDT (started with DDT wettable powder and replaced by DDT emulsion)

  1. - Abate 500 E was applied in drains and canals

  2. - Automatic siphons, tidal gates and sluice gates were constructed to manage water movement.

Health education for the community.

  • Active case detection in high-risk areas.

  • Passive case detection in patients seeking medical and health services.

  • Mass blood screenings

  • every 6 months in areas with increase of cases, influx of foreign workers, interior Orang Asli settlements and where there were cases in non-endemic areas.

  • Presumptive treatment (Darachlor (chloroquine/pyrimethamine)) was given to suspected cases, especially those from malarious areas before blood examination.

  • Radical and follow-up treatment (sulfadoxine/pyrimethamine, chloroquine and primaquine) was given for all reported cases.

Vertical organisational structure:

  1. - Director and deputy director

  2. - Administration bureau

  3. - Spraying bureau

  4. - Health education and training bureau

  5. - Epidemiology bureau

  6. - Entomology bureau

  7. - Malariologist

  8. - District chief and multi-purpose/special team

Specially trained personnel deployed to map and spray all houses and structures, perform

census counts, perform mass blood surveys and general

surveillance activities.

  • Case registries

  • Entomological surveillance activities to study vector habits.

  • Substantial decline in reported cases in West Malaysia and Sarawak, from 150,000 at the start of the programme to <50,000 a year in the late 1970s.

  • Did not succeed in eliminating malaria, re-orientated strategy to malaria control.

  • 1985: Incorporated into the Vector-Borne Disease Control Programme.

National Leprosy Control Programme Peninsular Malaysia (1969), Sarawak (1974), Sabah (1985)Early case finding by staff of the ‘skin clinics’.
  • Introduction of multiple drug therapy (MDT) and decentralisation of treatment:

  • patients were hospitalised only during the intensive phase of treatment, and follow-up treatment was available at 23 skin clinics throughout the country.

  • Institutional treatment only for infectious cases and non-infectious cases with severe reactions from drug cases requiring reconstructive surgery.

 A Central Registry of cases was established at the National Control Centre: it registered 50% or 8,710 estimated cases in 1969.Worked with MaLRA to reduce stigma and facilitate social integration of patients.1994: achieved WHO elimination status of <1 per 10,000 population.
  • National Immunisation Programme – Expanded Immunisation Programme was adopted as part of the National Immunisation Programme in the late 1980s.

  • Smallpox (early 1950s)

  • DPT (1958)

  • BCG (1961)

  • Poliomyelitis (1972)

  • Measles (1984)

  • Rubella (1988)

  • Hepatitis B (1989)

  • Immunisation campaigns jointly organised with NGOs.

  • Dissemination of health education messages through mass media.

  • Delivered through the rural health units or the MCH clinics in urban areas as part of MCH services.

  • Focus on low-coverage groups:

  • Estate population

  • Indigenous people

  • Religious subgroups

  • Urban poor

  • Defaulter tracing

  • Missed opportunities

  • Strengthening of the cold chain:

  • Provision of suitable refrigerators, ice packs and vaccine carriers

  • Training on the management, maintenance and monitoring of the cold chain

Development of a mapping system and improved monitoring system at district and local levels.
  • Almost 90% childhood immunisation coverage for BCG, DPT, polio and MMR in 1990

  • Decline of the infant and children mortality rate.

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