
| Training Manual in Combatting Childhood Communicable Diseases Part I (Peace Corps, 1985, 579 pages) |
| Module 2: Primary health care |
![]() | Session 5: Primary health care |
An Interim Strategy for Disease Control in Developing Countries
JULIA A. WALSH, M.D., AND KENNETH S. WARREN, M.D.
From the Rockefeller Foundation, 1133 Avenue of the Americas, New York, NY 10036, where reprint requests may be addressed to Dr. Warren.Presented at a meeting on Health and Population in Developing Countries, cosponsored by the Ford Foundation, the International Development Research Center and the Rockefeller Foundation and lead at the Bellagio Study and Conference Center, Lake Como, Italy, April, 1979.
Abstract. Priorities among the infectious diseases affecting the three billion people in the less developed world have been based on prevalence, morbidity, mortality and feasibility of control. With these priorities in mind a program of selective primary health care is compared with other approaches and suggested as the most cost-effective form of medical intervention in the least developed countries. A flexible program delivered by either fixed or mobile units might include measles and diphtheria-pertussis-tetanus vaccination, treatment for febrile malaria and oral rehydration for diarrhea in children, and tetanus toxoid and encouragement of breast feeding in mothers. Other interventions might be added on the basis of regional needs and new developments. For major diseases for which control measures are inadequate, research is an inexpensive approach on the basis of cost per infected person per year. (N Engl J Med 301:967-974, 1979)
THE three billion people of the less developed world suffer from a plethora of infectious diseases. Because these infections tend to flourish at the poverty level, they are important indicators of a vast state of collective ill health. The concomitant disability has an adverse effect on agricultural and industrial development, and the infant and child mortality inhibits attempts to control population growth.
What can be done to help alleviate a nearly unbroken cycle of exposure, disability and death? The best solution, of course, is comprehensive primary health care, defined at the World Health Organization conference held at Alma Ata in 1978 as
the attainment by all peoples of the world by the year 2000 of a level of health that will permit them to lead a socially and economically productive life. Primary health care includes at least: education concerning prevailing health problems and the methods of preventing and controlling them; promotion of food supply and proper nutrition, an adequate supply of safe water and basic sanitation; maternal and child health care, including family planning; immunization against the major infectious diseases; prevention and control of locally endemic diseases; appropriate treatment of common diseases and injuries; and provision of essential drugs.1
The goal set at Alma Ata is above reproach, yet its very scope makes it unattainable because of the cost and numbers of trained personnel required. Indeed, the World Bank has estimated that it would cost billions of dollars to provide minimal, basic (not comprehensive) health services by the year 2000 to all the poor in developing countries. The bank's president, Robert McNamara, offered this somber prognosis in his annual report in 1978:
Even if the projected - and optimistic - growth rates in the developing world are achieved, some 600 million individuals at the end of the century will remain trapped in absolute poverty. Absolute poverty is a condition of life so characterized by malnutrition, illiteracy, disease, high infant mortality and low life expectancy as to be beneath any reasonable definition of human decency.2
How then, in an age of diminishing resources, can the health and well-being of those "trapped at the bottom of the scale" be improved before the year 2000? A valid approach to this overwhelming problem can be based on the realization that the state of collective ill health in many of the less developed countries is not a single problem. Traditional indicators, such as infant mortality or life expectancy, do not permit a grasp of the issues involved, since they are actually composites of many different health problems and disorders. Each of the many diseases endemic to the less developed countries (Table 1) has its own unique cause and its own complex societal and scientific facets; there may be several points in the process for which interventions could be considered. 3-5
Thus, a rationally conceived, best-data-based, selective attack on the most severe public-health problems facing a region might maximize improvement of health and medical care in less developed countries. In the discussion that follows, we try to show the rationale and need for instituting selective primary health care directed at preventing or treating the few diseases that are responsible for the greatest mortality and morbidity in less developed areas and for which interventions of proved efficacy exist.
ESTABLISHING PRIORITIES FOR HEALTH CARE
Faced with the vast number of health problems of mankind, one immediately becomes aware that all of them cannot be attacked simultaneously. In many regions priorities for instituting control measures must be assigned, and measures that use the limited human and financial resources available most effectively and efficiently must be chosen. Health planning for the developing world thus requires two essential steps: selection of diseases for control and evaluation of different levels of medical intervention from the most comprehensive to the most selective.
Selecting Diseases for Control
In selecting the health problems that should receive the highest priorities for prevention and treatment, four factors should be assessed for each disease: prevalence, morbidity, mortality and feasibility of control (including efficacy and cost).
Table 2 incorporates these factors into an analysis of three representative illnesses of the less developed world. The newly discovered Lassa fever was associated with a 30 to 66 per cent mortality rate in the few limited outbreaks recorded in Nigeria, Liberia and Sierra Leone. Those who survived recovered fully after an illness lasting seven to 21 days. Although this fatality rate seems to suggest giving Lassa fever high priority in a major health program, the prevalence of overt disease appears to be low. Furthermore, the only treatment available is injections of serum from patients who have recovered. Since its mode of transmission is unknown and there is no vaccine, Lassa fever is impossible to control at present.6 Therefore, concentration on preventing Lassa fever would be neither efficient nor efficacious.
Ascaris, the giant intestinal roundworm, causes the most prevalent infection of man, with one billion cases throughout the world.7 Yet disability appears to be minor and death relatively rare.3,4 Treatment, however, requires periodic chemotherapy for an indefinite period.3,4,8 Control may ultimately require massive, long-term improvements in sanitary and agricultural practices to reduce reinfection. In view of the difficulty of eliminating exposure to the roundworm and the low morbidity associated with the infection, ascariasis deserves less attention than its ubiquity seems to suggest.
Malaria is associated with a far smaller mortality rate than that of Lassa fever and a far lower prevalence that that of ascariasis. Yet its mode of transmission is well known, and it produces much recurring illness and death; about one million children in Africa alone die annually from malaria.9 What also distinguishes malaria from Lassa fever and ascariasis is that it can be controlled through regular mosquito-spraying programs or chemoprophylaxis.3,9 Of these three infections, then, malaria would be as signed the highest priority for prevention in the most effective approach to reducing morbidity and mortality.
By means of the process outlined above for Lassa fever, ascariasis and malaria, the major infections endemic to the developing world (Table 1) were evaluated and assigned high (I), medium (II) or low (III) priorities. Within categories exact rank is not of major importance, and rank may change or items may be added or deleted, depending on the geographic area under consideration. For instance, schistosomiasis, to which a high priority was assigned, does not occur in many areas of the developing world. Our results and rationale for the proposed hierarchy are listed in Table 3.
Table 1. Prevalence, Mortality and Morbidity of the Major Infectious Diseases of Africa, Asia and Latin America, 1977-1978.*
|
INFECTION |
INFECTIONS (THOUSANDS/Yr) |
DEATHS (THOUSANDS/Yr) |
DISEASE (THOUSANDS OF CASES/Yr) |
AVERAGE No. OF DAYS OF LIFE LOST (PER CASE) |
RELATIVE PERSONAL DISABILITY** |
|
Diarrheas |
3-5,000,000 |
5-10,000 |
3-5,000,000 |
3-5 |
2 |
|
Respiratory infections |
4-5000 |
5-7 |
2-3 | ||
|
Malaria |
800,000 |
1200 |
150,000 |
3-5 |
2 |
|
Measles |
85,000 |
900 |
80,000 |
10-14 |
2 |
|
Schistosomiasis |
200,000 |
500-1000 |
20,000 |
600 1000 |
3-4 |
|
Whooping cough |
70000 |
254450 |
20,000 |
21-28 |
2 |
|
Tuberculosis |
1,000,000 |
400 |
7000 |
200-400 |
3 |
|
Neonatal tetanus |
120-180 |
100-150 |
120-180 |
7-10 |
1 |
|
Diphtheria |
40,000 |
50-60 |
700-90.0 |
7-10 |
1 |
|
Hookworm |
7 - 900 000 |
50-60 |
1500 |
100 |
4 |
|
South American trypanosomiasis |
12000 |
60 |
1200 |
600 |
2 |
|
Onchocerciasis | |||||
|
Skin disease |
Low |
2-5000 |
3000 |
3 | |
|
30,000 | |||||
|
River blindness |
20-50 |
200-500 |
3000 |
1-2 | |
|
Meningitis |
150 |
30 |
150 |
7-10 |
1 |
|
Amebiasis |
400,000 |
30 |
1500 |
7-10 |
3 |
|
Ascariasis |
800,000 1,000.000 |
20 |
1000 |
7-10 |
3 |
|
Poliomyelitis |
80,000 |
10-20 |
2000 |
3000+ |
2 |
|
Typhoid |
1000 |
25 |
500 |
14-28 |
2 |
|
Leishmaniasis |
12,000 |
5 |
12,000 |
100-200 |
3 |
|
African trypanosomiasis |
1000 |
5 |
10 |
150 |
1 |
|
Leprosy |
Very low |
12,000 |
500-3000 |
2-1 | |
|
Trichuriasis |
500,000 |
Low |
100 |
7-10 |
3 |
|
Filariasis |
250,000 |
Low |
2-3000 |
1000 |
1 |
|
Giardiasis |
200,000 |
Very low |
500 |
5-7 |
1 |
|
Dengue |
3 4000 |
0.1 |
1-2000 |
5-7 |
2 |
|
Malnutrition |
5-800,000 |
2000 |
* Based on estimates from the World Health Organisation and its Special Programme for Research and Training in Tropical Diseases, confirmed or modified by extrapolations from published epidemiologic studies performed in well defined populations (see references). Figures do not always match those officially reported, because under-reporting is great.
** 1 denotes bedridden, 2 able to function on own to some extent, 3 ambulatory, & 4 minor.
Table 2. An Approach to the Establishment Priorities for Disease Control, Based on Prevalence, Mortality, Morbidity and Feasibility of Control of Three Representative Infections.
|
Infection |
Prevalence |
Mortality |
Mortality |
Feasibility of control |
Priority |
|
Lassa fever |
Unknown (thought to be low) |
High (30-66%) |
Moderate (bedridden 7-21 days) |
Extremely poor al present |
Low prevalence low, feasibility of control poor |
|
Ascariasis |
Extremely high (thought to affect 1 billion people) |
Extremely low (approximately 0,001 %) |
Low (minor disability & often assymptomatic) |
Poor (continuous drug treatment required) |
Low: mortality & morbidity low, feasibility of control
poor |
|
Malaria |
High (more than 300 million infected annually) |
Low (approximately 0.1%) |
High (severe, many complications, often recurrent) |
Good (chemoprophylaxis available; regular spraying programs for
vectors practical) |
High: prevalence high, morbidity high, feasibility of control
good |
Group I contains the infections causing the greatest amount of most readily preventable illness and death: diarrheal diseases, malaria, measles, whooping cough, schistosomiasis and neonatal tetanus. With the exception of schistosomiasis, all the infections receiving highest priority for health-care planning affect young children more than adults.10-14 Together with respiratory infections and malnutrition, they account for most of the morbidity and mortality among infants and young children.11,15,17 Members of this age group (five years old or less) have a death rate many times greater than that of their counterparts in Western countries - accounting for 40 to 60 per cent of all mortality in most less developed countries.11,15,17 It infant and child deaths from these infections are reduced, a large decline in the overall death rate will result. Such a situation would be an optimal outcome of a selective disease-control program.
Groups II and III contain health problems that are either less important or more difficult to control. Respiratory infections, a major cause of disability and death, are not listed in Group I because of the difficulties involved in preventing and managing them. A wide variety of viruses and bacteria are associated with pulmonary infections, and no specific causative agent has been found in most patients.16,28 As in the industrialized world, where pneumonia is frequently the terminal episode in elderly patients weakened by cancer or cardiovascular disease, lower-respiratory-tract infections affect children in developing countries who are already afflicted with chronic malnutrition and parasitic infections.16 Pneumococcal and influenza vaccines prevent only a small percentage of cases, and influenza immunization must be given almost yearly because the virus changes antigenically. When penicillin injections were given to all children with clinical signs of pneumonia in the Narangwal Project in India, the mortality rate decreased by 50 per cent,21 but this method must be evaluated more extensively before it can be regarded as a major improvement in prevention of respiratory disease.
A medium or low priority was assigned if control measures were inadequate. For example, there is no acceptable therapy for chronic Chagas' disease.3,4 Only toxic drugs and procedures of unknown efficacy, such as nodulectomy, are available for treatment of onchocerciasis.3,4 Leprosy and tuberculosis require years of drug therapy and even longer follow-up periods to ensure cure.4,22,23 instead of attempting immediate, large-scale treatment programs for these infections, the most efficient approach may be to invest in research and development of less costly and more efficacious means of prevention and therapy. To reiterate, the most important factor in establishing priorities for endemic infections, even when evaluating diseases with high case rates, is a knowledge of which diseases contribute most to the burden of illness in an area and which are reasonably controllable.
Table 3. Priorities for Disease Control in the Developing World, Based on Prevalence, Mortality, Morbidity and Feasibility of Control.
|
Priority group |
Reasons roe Assignment to this category |
|
I High |
High prevalence, high mortality or high morbidity, effective
control |
|
Diarrheal diseases | |
|
Measles | |
|
Malaria | |
|
Whooping cough | |
|
Schistosomiasis | |
|
Neonatal tetanus | |
|
II Medium | |
|
Respiratory infections |
High prevalence, high mortality, no effective
control |
|
Poliomyelitis |
High prevalence, low mortality, effective control |
|
Tuberculosis |
High prevalence, high mortality, control
difficult |
|
Onchocerciasis |
Medium prevalence, high morbidity, low mortality, control
difficult |
|
Meningitis |
Medium prevalence, high mortality, control
difficult |
|
typhoid |
Medium prevalence, high mortality, control
difficult |
|
Hookworm |
High prevalence, low mortality, control difficult |
|
Malnutrition |
High prevalence, high morbidity, control complex |
|
III Low | |
|
South American trypanosomiasis (Chagas' disease) |
Control difficult |
|
African trypanosomiasis |
Low prevalence, control difficult |
|
Leprosy |
Control difficult |
|
Ascariasis |
Low mortality, low morbidity, control difficult |
|
Diphtheria |
Low mortality, low morbidity |
|
Amebiasis |
Control difficult |
|
Leishmaniasis |
Control difficult |
|
Giardiasis |
Control difficult |
|
Filariasis |
Control difficult |
|
Dengue |
Control difficult |
EVALUATING AND SELECTING MEDICAL INTERVENTIONS
Once diseases are selected for prevention and treat. meet, the next step is to devise intervention programs of reasonable cost and practicability. The interventions relevant to the world's developing areas that are considered below are comprehensive primary health care (which includes general development as well as all systems of disease control), basic primary health care, multiple disease-control measures (e.g., insecticides, water supplies), selective primary health care, and research. Below is a discussion of each approach, with emphasis on the relative cost involved in undertaking and maintaining these programs and on the benefits that have accrued.
This section of our analysis relies on reported results from individual studies conducted in various parts of the world. In addition, we have examined estimates of cost and effectiveness in terms of expected deaths averted by each intervention for a model area in Africa. The model area is an agricultural, rural portion of Sub-Saharan tropical Africa with a population of about 500,000 (100,000 are five years old or less). For reference purposes, the average figures for Sub-Saharan Africa will be used: the birth rate is 46 per thousand total population, the crude death rate 19 per thousand total population, and the infant mortality rate 147 per thousand live births.24,25
Comprehensive versus Basic Primary Health Care
Comprehensive primary health care for everyone is the best available means of conquering global disease, the humane and noble goal declared at Alma Ata. As defined by the World Health Organization, this system encompasses development of all segments of the economy, ready and universal access to curative care, prevention of endemic disease, proper sanitation and safe water supplies, immunization, nutrition, health education, maternal and child care and family planning. Since resources available for health programs are usually limited, the provision of comprehensive primary health care to everyone in the near future remains unlikely.
Basic primary health-care systems are far more circumscribed in their goals, which are to provide health workers and establish clinics for treating all illnesses within a population. Nevertheless, this approach is far from inexpensive. The World Bank has estimated that the cost of furnishing basic health services to all the poor in developing countries by the year 2000 will be $5.4 to $9.3 billion (in 1975 prices).24 This investment, which includes only initial capital investment and training costs, would provide one community health worker or auxiliary nurse-midwife for every 1500 to 2000 people and one health facility for every 8000 to 12,000 people or every 10 km2, whichever is greater. In the model area in Africa, the World Bank estimated that supplying the minimum care offered by building one health post with one vehicle per 10,000 people and training 125 auxiliary nurse-midwives and 250 community health workers would cost $2,500,000, or $5 per capita. To this figure must be added the recurrent costs of salaries, drugs, supplies and maintenance. Other costs not included are for training facilities, continuing education, expansion of referral services and development of communication, transportation and administrative networks to supply and manage the health facilities. Furthermore, the effectiveness of this model program for averting deaths or applying such preventive measures as education in sanitation and nutrition has not been clearly established.
The pilot projects for providing basic health-cam services that have been evaluated vary in their effectiveness in improving the general level of health care. For example, an outside evaluation of primary health service in Ghana revealed that a third to half the population of the districts lived outside the effective reach of health units providing primary care. Only about one fifth of the births were supervised by trained midwives; only one fifth of the children under the age of five years had been seen in a child-health clinic, and two thirds of the population lacked environmental sanitation services. Furthermore, the services were often of poor quality, notably in the crucial area of child care.27,28
The cost and effectiveness of several experimental programs providing primary health care in localized areas have been compared in Imesi, Nigeria29; Etimesgut, Turkey30,31; Narangwal, India21; Jamkhed, India32,33; Guatemalan villages34; Hanover, Jamaica35-37; and Kavar, Iran.38 The estimated cost per capita varied widely among the programs, particularly because they were initiated at different times over the past 15 to 20 years and furnished different services to their communities. In general, however, the cost per capita ranged between l and 2 per cent of the national per capita income of the particular country. The cost For infant deaths averted were difficult to compare because of the paucity of control groups and inconsistency of the population groups monitored. Figures ranged from $144 to $20,000, with a median of $700. The only precise calculations for the costs per infant death averted ($144) or child death evened ($988 per one to three-year-old child) were for a medical-care and nutrition-supplementation project in Narangwal, India.21 The estimates were much higher for deaths averted by nutrition supplements.
Under some circumstances, programs of basic primary health care have been successful, but the cost and the degree improvement in community health have varied markedly enough that refinements in the approach are still needed.
Multiple Disease-Control Measures
These interventions, which include vector control, water and sanitation programs and nutrition supplementation, are more specific and easily managed than primary health-care programs, and they control many similarly transmitted diseases simultaneously. They can decrease mortality and morbidity and have served as interim strategies for health care in less developed countries.
Vector Control
Vector control is directed at managing the insects and mollusks that carry human disease. This approach has the advantage of being comparatively inexpensive, but it must be continued indefinitely and may be ephemeral since the vectors tend to become resistant. The examples below reveal some of the complexities of maintaining vector control.
The control of malaria transmission through insecticides has been highly effective. In the tropical regions and savannas of Africa, twice-yearly spraying has decreased the crude death rate by approximately 40 per cent and infant mortality by 50 per cent.39-41 The World Health Organization has estimated that the average cost for house-to-house spraying with chlorophenothane (DDT) is $2 per capita annually.9 Therefore, the cost per adult and infant death averted is $250, and the cost per infant death averted is $600. Unfortunately, eradication of malaria with insecticides is becoming more difficult to accomplish. Because mosquitoes can be expected to become resistant to DDT within a few years, other, much more expensive pesticides must be substituted; the use of propoxur or fenetrithion will raise the cost of the chemicals five to 10 times.9 Furthermore, there is no way of knowing how long these insecticides will remain toxic to the mosquitoes. Among the mosquitoes in which widespread resistance to insecticides has developed are Culex pipiens fatigans the major vector of urban filariasis, and Aedes aegypti, the vector of yellow fever and dengue.5
Two other vector-control programs illustrate the prolonged maintenance required by this type of health intervention. Onchocerciasis, a potentially blinding helminth infection affecting 30 million people in Africa, is being managed in the Volta River Basin through a 20-year larvicide operation to control the blackfly vector. The program is estimated to cost $18 per capita for the entire 20-year period or $.90 per capita per year.26 Disability will be prevented, and economic activity in the area may increase if the program is successful, but continuous, indefinite applications of insecticide will be necessary. Since 1965, St. Lucia has had a program to control the snail-transmitted helminth infection schistosomiasis through molluscicides. An annual cost per capita of about $3.70 and good results have been reported: the prevalence of the infection has decreased from 45 to 35 per cent in adults and born 21 to 4 per cent in children. Despite these heartening figures, eradication of the vector cannot be considered on the horizon. Schistosomiasis is a long-term, chronic infection and the death rate will not begin to decline until many years after continuous mollusk control.
Water and Sanitation Programs
Proper sanitation and clean water make a substantial difference in the amount of disease in an area, but the financial investment involved is enormous. The success of such projects also depends on rigorous maintenance and alteration of engrained cultural habits.
With the installation of community water supplies and sanitation in developing areas, deaths from typhoid can be expected to decrease 60 to 80 per cent,43 deaths from cholera 0 to 70 per cent,43-48 from other diarrheas 0 to 5 per cent,48-51 from ascaris and other intestinal helminths 0 to 50 per cent8,10,52-54 and from schistosomiasis 50 per cent42,52 (after 15 to 20 years). The World Bank has estimated that the cost of providing community water supplies and sanitation to all those in need by the year 2000 will be $135 to $260 billion.26,35 Construction of a rural community stand-pipe costs $20 to $26 per capita, and rural sanitation costs $4 to $5 per capita. In urban areas the costs are $31 and $23, respectively. In our model area of Sub-Saharan Africa the initial investment would be $12 to $15 million if amortization and annual maintenance costs are only 10 per cent of this sum, the annual cost per deaths averted will be $2400 to $2900, and the cost per infant and child deaths averted will be $3600 to $4300.
What must be realized is that the above sums are largely for public standpipes, which are not highly effective in reducing morbidity and mortality from water-related diseases. It is well documented that connections inside the house are necessary to encourage the hygienic use of water.56 For example, shigella-caused diarrheas decreased 5 per cent with outside house connections but fell 50 per cent when sanitation and washing facilities were available within the home.51
All these estimates depend on exclusive use of protected sanitation and water supplies, without continuing use of environmental sources. In Bangladesh for example, there was no reduction in cholera in areas supplied with tube wells, primarily because of the use of contaminated surface water as well as the protected water supply.47 In St. Lucia, contact with surface water could not be discouraged until household water supplies and then swimming pools and laundry units were installed, and an intensive health-education campaign was instituted.42 In other words, changing peoples' habits in excretion and water usage takes more than introducing an adequate, dependable and convenient new source. Realistically speaking, a pervasive and effective health-education campaign37,38 is required.
Nutrition Supplementation
Nutrition programs have been advocated as among the most efficient means of decreasing morbidity and mortality in children, but supplementation alone has had no notable effect. Malnutrition is an underlying or associated factor in many deaths from infections in children; in a group of Latin American children, it was associated in 50 per cent of the cases.39 Poor nutrition may also increase susceptibility to disease or predispose an infected child to more severe illness.60-62 Conversely, infection may be a prominent cause of poor nutrition61,63-66 since less food is ingested and absorbed by a sick child. Therefore, if infections could be controlled it is probable that the nutritional status of children would improve greatly. There have been some situations, however, in which malnutrition has been reported to protect against certain infections, e.g., the Sahel famine was thought to suppress malaria, and iron deficiency was reported to protect against bacterial intections.67-76
In view of these findings, it is not surprising that few nutrition-supplementation programs alone have effected a major decrease in the death rate. The Narangwal Project is one of these few, but even in that program the cost per death averted in infants was $213. In children one to three years old the cost was $3000 - 1.5 to three times higher than the cost of medical care alone.21
Selective Primary Health Care
The selective approach to controlling endemic disease in the developing countries is potentially the most cost-effective type of medical intervention. On the basis of high morbidity and mortality and of feasibility of control, a circumscribed number of diseases are selected for prevention in a clearly defined population. Since few programs based on this selective model of prevention and treatment have been attempted, the following approach is proposed. The principal recipients of care would be children up to three years old and women in the childbearing years. The care provided would be measles and diphtheria-pertussis-tetanus (DPT) vaccination for children over six months old, tetanus toxoid to all women of childbearing age, encouragement of long-term breast feeding, provision of chloroquine for episodes of fever in children under three years old in areas where malaria is prevalent and, finally, oral rehydration packets and instruction.
If even 50 per cent of the children and their mothers and 50 per cent of the pregnant women in a community were contacted, deaths from measles would be expected to decrease at least 50 per cent,71,72 deaths from whooping cousin 30 per cent,73 from neonatal tetanus 45 per cent,74 from diarrhea 25 to 30 per cent75,76 and from malaria 25 per cent.9 Oral rehydration has been used successfully in hospitals,77,78 in out patient clinics79 and recently in the home75,76 to treat diarrheas of numerous causes.
These services could be provided by fixed units or by mobile teams visiting once every four to six month in areas where resources were more limited. Mobile units have been successfully used in immunization programs for smallpox and measles,80,81 in treatment services directed against African trypanosomiasis and meningitis82 and in provision of child care in rural areas.83-85
The cost of fixed units would be similar to that of basic primary health care, although efficiency should be much greater. Cost estimates for a mobile health unit used in the model area in Africa for malaria control and water and sanitation programs were based on an extensive study of the Botswana health services by Gish and Walker.85 They estimated $1.26 as the cost per patient contact in 1974, on a sample 306-km trip that reached 753 patients; the estimated cost per infant and child death averted was $200 to $250. Medications accounted for 30 to 50 per cent of this cost, but this figure could be decreased with contributions of drugs from abroad or their manufacture within the country.
Whether the system is fixed or mobile, flexibility is necessary. The care package can be modified at any time according to the patterns of mortality and morbidity in the area served. Chemotherapy for intestinal helminths, treatment of schistosomiasis and supplementation with new vaccines or treatments as they become available are all types of selective primary health care that could be added or subtracted to this core of basic preventive care. It is important, however, for the service to concentrate on a minimum number of severe problems that affect large numbers of people and for which interventions of established efficacy can be provided at low cost.
Research
For a number of prevalent infections, treatment or preventive measures are expensive, difficult to administer, toxic or ineffective. These infections, which include Chagas' disease, African trypanosomiasis, leprosy and tuberculosis, may better be dealt with through an investment in research. In terms of the potential benefits, the cost of research is low. Indeed, the total amount now being spent on research in all tropical diseases is approximately $60 million, exceedingly small in relation to the number of people infected. As Table 4 shows, expenditures for research on some of the major diseases in the developing world have by far the lowest per-capita cost of all medical interventions discussed.84
The estimated cost for the research and development leading to the pneumococcal vaccine licensed in the United States in 1978 was $3 to $4 million (Austrian R: personal communication). Death and disability in developing countries would be reduced by heat-stable vaccines for measles, malaria, leprosy and rotavirus and Escherichia coli-induced diarrheas, by improved chemotherapy for leprosy, tuberculosis, American and African trypanosomiasis, onchocerciasis and filariasis and by depot drugs [or malaria and intestinal helminths.
Table 4. Research Funding for Major Diseases of the Developing World, 1978.
|
Infection |
Amount of Funding ($) |
Cost/Infected Person/Yr ($) |
|
Malaria |
15,000,000 |
0.02 |
|
Schistosomiasis |
7,000.000 |
0.04 |
|
Filariasis |
2,000,000 |
0.01 |
|
Trypanosomiasis |
5,000,000 |
0.38 |
|
Leishmaniasis |
1,200,000 |
0.10 |
|
Leprosy |
2,000,000 |
0.16 |
CONCLUSIONS
Until comprehensive primary health care can be made available to all, services aimed at the few moss important diseases (selective primary health care) may be the most effective means of improving the health of the greatest number of people. The crucial point is how to measure the effectiveness of medical interventions. In all the foregoing calculations, we based our analysis of cost effectiveness on changes in mortality or deaths averted. We did not measure the illness and disability that would be prevented. No other benefits For which intervention may have been responsible were measured because they are much more difficult to quantify. The inadequacy of available data makes it impossible to measure distinct and undeniable secondary benefits. For example, water supplies close by would save time for the women who carry water, and increased amounts could irrigate a home garden.
Accordingly, Table 5 summarizes the estimated costs per capita and per death averted for the various health interventions considered. The per capita costs are calculated in terms of the entire infant, child and adult population or the area covered by the service. A-5 the table Suggests, selective primary health care may be a cost-effective interim intervention For many less developed areas.
Table 5. Estimated Annual Costs of Different Systems of Health Intervention.
|
Intervention |
Per Capita cost ($) |
Cost per infant and/or Child Death Averted*
($) |
|
Basic primary health care ** | ||
|
Range |
0.40-7.50 |
144-20,000 (I) |
|
Median |
2.00 |
700 |
|
Mosquito control for malaria |
2 00 |
600 (I) |
|
Onchocerciasis control program |
0.50 |
Few infant & child deaths |
|
Mollusk control for schistosomiasis |
3.70 |
Few infant & child deaths |
|
Community water supplies & sanitation |
30-54 |
3600-4300 (I,C) |
|
Narangwal nutrition |
1.75 |
213(I) |
|
supplementation |
3000 (C) | |
|
Selective primary health care *** |
0.25 |
200 250 (I,C) |
* I denotes infant & C child.
** Delivered by village
health workers
*** In this case, delivered by mobile units
REFERENCES
1. World Health Organization: Declaration of Alma Ata (Report on the International Conference Primary Health Care, Alma Ala USSR, September 6-12, 1978). Geneva, World Health Organization, 1978
2. McNamara RS: Address to the Board of Governors of the World Bank Washington, DC, World Bank, 1978
3. Geographic Medicine for the Practitioner Algorithms in the diagnosis and management of exotic diseases. Edited by KS Warren, AAF Mahmoud. Chicago, University of Chicago Press, 1978
4. Tropical Medicine. Edited by GW Hunter III, JC Swartzwelder, DF Clyde. Fifth edition. Philadelphia, WB Saunders Company, 1976
5. Resistance of vectors and reservoir of disease to pesticides: twenty-second report of the WHO Expert Committee on Insecticides. WHO Tech Rep Ser 585:1-88, 1976
6. Viral Infections of Humans Epidemiology and control Edited by AS Evens. New York, Plenum Medical Book Company, 1976
7. Peters W: Medical aspects - comments end discussion II, The Relevance of Parasitology to Human Welfare Today (Symposia of the British Society for Parasitology. Vol 16). Edited by ERA Taylor, R Mullet. Oxford, Blackwell Scientific Publications, 1978, pp 25-41
8. Arfaa F. Sahba GH, Farahmandian I: Evaluation of the effect of different methods of control of soil-transmitted helminths in Khuzestan, southwest Iran. Am J Trop Med Hyg 26:230-233, 1977
9. WHO Expert Committee on Malaria: sixteenth report. WHO Tech Rep Ser 549:1-89, 1974
10. Preston SH, Keyfitz, N. Schoen R: Clutter of Death Life tables for national populations New York, Seminar Press, 1972
11. Wyon JB, Gordon JE: The Khana Study: Population problems in the rural Punjab. Cambridge, Massachusetts, Harvard University Press, 1971
12. Ongom VL, Bradley DJ: The epidemiology and consequence of Schistosoma mansoni infection in West Nile, Uganda. I. Field studies, of a community at Panyogoro. Trans R Soc Trop Med Hyg 66:835-851, 1972
13. Farooq, M, Samaan SA, Nielsen T: Assessment of seventy of disease caused by Schistosoma haematobium and S. mansoni in the Egypt-49 project area. Bull WHO 35:389-404, 1966
14. Siongok TKA, Mahmoud AAF, Ouma JH, et al: Morbidity in Schistosomiasis mansoni in relation to intensity of infection: study of a community in Machakos, Kenya Am J Trop Med Hyg 25:273-284, 1976
15. Hull TH, Rohde JE: Prospects for Rapid Decline of Mortality Rates in Java: A study of causes of death and the feasibility of policy interventions for mortality control. Yogyakarta, Indonesia, Population Institute, Gadjah Made University, 1978
16. Bulls A, Hitze KL: Acute respiratory infections: a review. Bull WHO 56:481-498, 1978
17. Dyson T: Levels, trends, differentials and causes Child mortality - a survey. World Health Stat Rep 30:282-311, 1977
18. Preston SH: Mortality Patterns in National Populations: With special reference to recorded causes of death. New York, Academic Press, 1976
19. United Nations Demographic Yearbook 1974. New York, United Nations, 1975
20. Sobëslawsky O, Sebikari SRK, Harland PSEG, et al: The viral etiology of acute respiratory infections in children in Uganda. Bull WHO 55:625-631, 1977
21. Taylor CE, Kielmann AA, Parker RL et al: Malnutrition, Infection Growth and Development The Narangwal experience final report. Washington, DC, World Bank, 1978
22. Fox W, Mitchison DA: Short course chemotherapy for pulmonary tuberculosis. Am Rev Respir Dis 111:845-848; 329-352, 1975
23. WHO Expert Committee on Leprosy: fifth report. WHO Tech Rep Ser 607:1-48, 1977
24. Kane TT, Myers PF: 1978 World Population Data Sheet Washington, DC, Population Reference Bureau, 1978
25. United Nations Demographic Yearbook 1976. Geneva, World Health Organization, 1977
26. Burki SJ, Voorhoeve JJC, Layton R. et al: Global Estimates for Meeting Basic Needs: Background paper (Basic Needs Paper No. 1). Washington, DC, World Bank, 1977
27. Institute of Development Studies Research Reports Health Needs and Health Services in Rural Ghana. Brighton, England, University of Sussex, 1978
28. Primary care in Ghana. Lancet 2:1085, 1978
29. Cunningham NJ: The under fives clinic - what difference does it make. J Trop Pediatr (in press)
30. Fisek NH: An Account of the Activities of the Etimesgut Rural Health District 1967, 1968s, and 1969. Ankara, Hacettepe Press and Hacettepe University School of Medicine, Institute of Community Medicine, 1970
31. Idem: An Account of the Activities of the Etimesgut Rural Health District 1970-1974. Ankara, Ayyildiz Matbaasi and Hacettepe University School of Medicine, Institute of Community Medicine, 1975
32. Arole M, Arole R: A comprehensive rural health project in Jamkhed (India), Health by the People. Edited by KW Newell. Geneva, World Health Organization, 1975, pp 70-90
33. Gwatkin DR, Wilcox JR, Wray JD. Can Intervention Make a Difference?: The policy implications of field experiment experience: a report to the World Bank. Washington, DC, World Bank, 1978
34. Working Group on Rural Medical Care: Delivery of primary care by medical auxiliaries: techniques of use and analysis, of benefits achieved in some rural villages in Guatemala, Medical Auxiliaries: Proceedings of a symposium held during the twelfth meeting of toe PAHO Advisory Committee on Medical Research, June 25,1973. Washington, DC, Pan American Health Organization, 1973, pp 24-40
35. Alderman MH, Husted J. Levy B. et al: A young-child nutrition programme in rural Jamaica. Lancet 1:1166-1169, 1973
36. Alderman MH, Cadien DS, Haughton PBH, et at: A student rural health project in Jamaica. West Indian Med J 21(1):20-24, 1972
37. Alderman M H. Wise PH, Ferguson RP, et al: Reduction of young child malnutrition and mortality in rural Jamaica. J Trop Pediatr 24:7-11, 1978
38. Ronaghy HA: Kavar village health worker project. J Trop Pediatr 24:13-60, 1978
39. Kouznetsov RL: Malaria control by application of indoor spraying of residual insecticides in tropical Africa and its impact on community health. Trop Doct 7:81-91, 1977
40. Payne D, Grab B, Fontaine RE, et al: Impact of control measures on malaria transmission and general mortality. Bull WHO 54:369-377, 1976
41. Fontaine RE, Pull JH, Payne D, et al: Evaluation of fenitrithion for the control of malaria. Bull WHO 56:445-452, 1978
42. Jordan P: Schistosomiasis - research to control. Am J Trop Mod Hyg 26:877-886, 1977
43. Zaheer M, Prasad BG, Govil KK, et al: A note on urban water supply in Uttar Pradesh. J Indian Med Assoc 38:17-82, 1962
44. Azurin JC, Alvero M: Field evaluation of environmental sanitation measures against cholera. Bull WHO 51:19-26, 1974
45. Wolff HL, Van Zijl WJ: Houseflies, the availability of water, and diarrhoeal disease. Bull WHO 41:952-959, 1969
46. Briscoe J: The role of water supply in improving health in poor countries (with special reference to Bangladesh). Am J Clin Nutr 31:2100-2113, 1978
47. Sommer A, Woodward WE: The influence of protected water supplies on the spread of classical-Inaba and El Tor-Ogawa cholera in East Bengal. Lancet 2:985-987, 1972
48. Levine RJ, Khan MR, D'Souza S, et al: Failure of sanitary wells to protect against cholera and other diarrhoeas in Bangladesh. Lancet 2:86-89, 1976
49. Schneider R E, Shiffman M, Faigenblum J: The potential effect of water on gastrointestinal infections prevalent in developing countries. Am J Clin Nutr 31:2089-2099, 1978
50. Feachem R, Burn E. Cairncross S, et al: Water, Health and Development. London, Tri-Med Books, 1978
51. Hollister AC Jr, Beck MD, Gittlesohn AM, et al: Influence of water availability on Shigella prevalence in children of farm labor families. Am J Public Health 45:354-362, 1955
52. Khalil M: The relation between sanitation and parasitic infections in the tropics. J R Sanit Inst 47:210-215, 1926
53. Chandler AC: A comparison of helminthic and protozoan infections in two Egyptian villages two years after the installation of sanitary improvements in one of them. Am J Trop Med Hyg 3:59-73, 1954
54. Schliessmann DJ, Atchley FO, Wilcomb MJ Jr, et al: Relation of Environmental Factors to the Occurrence of Enteric Diseases in Areas of Eastern Kentucky (PHS Publication No. 591). Washington, DC, Government Printing Office, 1958, pp 1-35
55. Appropriate Technology for Waste Supply and Waste Disposal in Developing Countries. Washington, DC, World Bank. 1977
56. White GF, Bradley DJ, White AU: Drawers of Water: Domestic water use in East Africa. Chicago, University of Chicago Press, 1972
57. Wolman A: Environmental sanitation in urban and rural areas: its importance in the control of enteric infections. Bull Pan Am Health Organ 9:157-159, 1975
58. Gordon JE, Béhar M, Scrimshaw NS: Acute diarrhoeal disease in less developed countries. 3. Methods for prevention and control. Bull WHO 31:21-28, 1964
59. Puffer RR, Serrano CV: Patterns of Mortality in Childhood. Washington, DC, Pan American Health Organisation, 1973
60. Mata LJ: Th Children of Santa Mariá Cauqué: A prospective field study of health and growth. Cambridge, Massachusetts, MIT Press, 1978
61. Idem: The malnutrition-infection complex and its environmental factors. Presented at the Symposium on Protein-Energy Malnutrition sponsored by The Nutrition Foundation, London, September, 1978
62. Mata L.J., Kronmal RA, Garcia B: Breast-feeding weaning and the diarrhoeal syndrome in a Guatemalan Indian village. Ciba Found Symp 42:311-338, 1976
63. Condon-Paoloni D, Cravioto J, Johnston FE, et al: Morbidity and growth of infants and young children in a rural Mexican village. Am J Public Health 67:651-656, 1977
64. Martorell R, Habicht J-P, Yarbrough C, et al: Acute morbidity and physical growth in rural Guatemalan children. Am J Dis Child 129:1296-1301, 1975
65. Whitehead RG: Some quantitative considerations of importance to the improvement of the nutritional status of rural children. Proc R Soc Lond [Biol] 199:49-64, 1977
66. Rowland MGM, Cole TJ, Whitehead RG: A quantitative study into the role of infection in determining nutritional status in Gambian village children, Br J Nutr 37:441-450, 1977
67. Scrimshaw NS, Taylor CE, Gordon JE: Interactions of nutrition and infection. Am J Med Sci 237:367-403, 1959
68. Murray MJ, Murray AB, Murray NJ, et at: Refeeding - malaria and hyperferraemia. Lancet 1:653-654, 1975
69. Murray MJ, Murray AB, Murray MB, et at: The adverse effect of iron repletion on the course of certain infections. Br Med J 2:1113-1115, 1978
70. Murray J, Murray A, Murray M, et al: The biological suppression of malaria: an ecological and nutritional interrelationship of a host and two parasites. Am J Clin Nutr 31:1363-1366, 1978
71. Clinical trial of live measles vaccine given atone and five vaccine preceded by killed vaccine: fourth report to the Medical Research Council by the Measles Sub-committee of the Committee on Development of Vaccines and Immunisation Procedures. Lancet 2:571-575, 1977
72. Ministry of Health of Kenya and the World Health Organization: measles immunity in the first year after birth and the optimum age for vaccination in Kenyan children. Bull WHO 55:21-30, 1977
73. Mahieu JM, Muller AS, Voorhoeve AM, et al: Pertussis in a rural area of Kenya: epidemiology and a preliminary report on vaccine trial. Bull WHO 56:773-780, 1978
74. Kielmann AA, Vohra S: Control of tetanus neonatorum in rural communities - immunization effects of high-dose calcium phosphate adsorbed tetanus toxoid. Indian J Med Res 66:906-916, 1977
75. Kielmann AA, McCord C: Home treatment of childhood diarrhea in Punjab villages. J Trop Pediatr 23:197-201, 1977
76. Rohde JE; Preparing for the next round: convalescent care after acute infection. Am J Clin Nutr 31:2258-2268, 1978
77. Nalin DR, Levine MM, Mata L, et al: Comparison of sucrose with glucose in oral therapy of infant diarrhoea. Lancet 2:277-279, 1978
78. Chatterjee A, Mahalanabis D, Jalan KN, et al: Oral rehydration in infantile diarrhoea: controlled trial of a low sodium glucose electrolyte solution. Arch Dis Child 53:284-289, 1978
79. Mahalanbis D, Choudhuri AB, Bagchi NG, et al: Oral fluid therapy of cholera among Bangladesh refugees. Johns Hopkins Med J 132:197-205, 1973
80. Foege WH: Evaluation of Smallpox Eradication/Measles Control Program - The Gambia. Atlanta, National Communicable Disease Center, 1968
81. Idem: Measles Vaccination in Africa: Proceedings - International Conference on the Application of Vaccines against Viral, Rickettsial, and Bacterial Diseases of Man. Washington, DC, Pan American Health Organization, 1971, pp 207-221
82. Gonzalez CL: Mass Campaigns and General Health Services. Geneva, World Health Organization, 1965
83. Van Der Mei J, Belcher DW: Comparing under-five programmes in a hospital-based clinic and in satellite mobile clinics. Trop Geogr Med 26:449-456, 1974
84. Wilkinson JL, Smith H, Smith OI: The organization and economics of a mobile child welfare team in Sierra Leone. J Trop Med Hyg 70:14-18, 1967
85. Gish O, Walker G: Mobile Health Services. London, Tri-Med Books, 1977
86. World Health Organisation: Report of the Meting of Technical Review Group III, Geneva, 28 Aug. - 1 Sept. 1978: UNDP/World Bank/WHO Special Programme for Research and Training in Tropical Diseases. Geneva, World Health Organization, 1978
(From: The New England Journal of Medicine. Boston. Vol. 301, No. 18, pp. 967-974 )