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Estrategia de atención integrada de las enfermedades prevalentes de la infancia (AIEPI) para niños menores de cinco años

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Resumen

Antecedentes

Más de 7 500 000 niños menores de cinco años de edad que viven en países de ingresos bajos y medios mueren cada año. La Organización Mundial de la Salud (OMS) desarrolló la estrategia de atención integrada de las enfermedades prevalentes de la infancia (AIEPI) para reducir la mortalidad y la morbilidad y para mejorar la calidad de la atención al mejorar la administración de diversas intervenciones curativas y preventivas médicas y conductuales en los establecimientos de salud, en el domicilio y en la comunidad.

Objetivos

Evaluar los efectos de los programas que implementan la estrategia de AIEPI en cuanto a la muerte, el estado nutricional, la calidad de la atención, la cobertura con materiales para la AIEPI y la satisfacción de los beneficiarios.

Métodos de búsqueda

Se hicieron búsquedas en el Registro Cochrane Central de Ensayos Controlados (Cochrane Central Register of Controlled Trials) (CENTRAL; 2015, número 3), incluyendo el registro especializado del Grupo Cochrane para una Práctica y Organización Sanitaria Efectivas (Cochrane Effective Practice and Organisation of Care Group‐ EPOC); MEDLINE; EMBASE, Ovid; Cumulative Index to Nursing and Allied Health Literature (CINAHL), EbscoHost; Latin American Caribbean Health Sciences Literature (LILACS), Virtual Health Library (VHL); WHO Library & Information Networks for Knowledge Database (WHOLIS); Science Citation Index and Social Sciences Citation Index, Institute for Scientific Information (ISI) Web of Science; Population Information Online (POPLINE); WHO International Clinical Trials Registry Platform (WHO ICTRP); y la base de datos Global Health, Ovid and Health Management, ProQuest. Se realizaron búsquedas hasta el 30 de junio 2015 y se complementaron buscando en las bibliografías revisadas y mediante contacto con expertos para identificar estudios en curso y no publicados.

Criterios de selección

Se intentó incluir los ensayos controlados aleatorios (ECA) y los estudios controlados tipo antes y después (controlled before‐after) (ECAD) con al menos dos sitios de intervención y dos sitios control que evaluaran la estrategia de AIEPI genérica o su adaptación en niños menores de cinco años de edad y que incluyeran esfuerzos mínimos para mejorar las habilidades de los trabajadores sanitarios para el tratamiento de los casos. Se excluyeron los estudios en los cuales la AIEPI se acompañó de otras intervenciones que incluyeron transferencias de dinero en efectivo condicionadas, administración complementaria de alimentos y empleo. El grupo de comparación recibió servicios sanitarios habituales sin la provisión de AIEPI.

Obtención y análisis de los datos

Dos autores de la revisión de forma independiente revisaron las búsquedas, seleccionaron los ensayos, y extrajeron, analizaron y tabularon los datos. Se utilizó la varianza inversa para los ensayos grupales y un coeficiente intragrupal de 0,01 cuando en el estudio primario no se había realizado el ajuste. Se utilizó el enfoque GRADE (Grades of Recommendation, Assessment, Development and Evaluation Working Group) para evaluar la seguridad de las pruebas.

Resultados principales

Dos ensayos aleatorios grupales (India y Bangladesh) y dos estudios controlados tipo antes y después (Tanzania e India) cumplieron los criterios de inclusión. Las estrategias incluyeron adiestramiento del personal de asistencia sanitaria, fortalecimiento de la administración de los sistemas de asistencia sanitaria (los cuatro estudios) y visitas al domicilio (dos estudios). Los dos estudios de la India incluyeron paquetes de atención dirigidos al período neonatal.

Un ensayo en Bangladesh calculó que la mortalidad en la niñez puede ser 13% inferior con la AIEPI, pero el intervalo de confianza (IC) incluyó ningún efecto (cociente de riesgos [CR] 0,87; IC del 95%: 0,68 a 1,10; 5090 participantes; pruebas poco confiables). Un ECAD en Tanzania proporcionó cálculos casi idénticos (CR 0,87; IC del 95%: 0,72 a 1,05; 1932 participantes).

Un ensayo en la India examinó la mortalidad infantil y neonatal al implementar la estrategia de atención integrada de las enfermedades prevalentes neonatales y de la infancia (AIEPNI) que incluye las visitas posnatales al domicilio. La mortalidad neonatal e infantil puede ser inferior en el grupo de AIEPNI en comparación con el grupo control (cociente de riesgos instantáneos [CRI] de la mortalidad infantil 0,85; IC del 95%: 0,77 a 0,94; CRI de la mortalidad neonatal 0,91; IC del 95%: 0,80 a 1,03; un ensayo, 60 480 participantes; pruebas poco confiables).

Se calculó el efecto de la AIEPI sobre cualquier mortalidad medida al combinar la mortalidad infantil y en la niñez en un ensayo de AIEPI y en un ensayo de AIEPNI. La mortalidad se puede reducir mediante la AIEPI (CR 0,85; IC del 95%: 0,78 a 0,93; dos ensayos, 65 570 participantes; pruebas poco confiables).

Dos ensayos (India, Bangladesh) evaluaron el estado nutricional y señalaron que puede haber poco o ningún efecto sobre el deterioro del crecimiento (CR 0,94; IC del 95%: 0,84 a 1,06; 5242 participantes, dos ensayos; pruebas poco confiables) y probablemente hay poco o ningún efecto sobre la emaciación (CR 1,04; IC del 95%: 0,87 a 1,25; dos ensayos, 4288 participantes; pruebas de confiabilidad moderada). El ECAD de Tanzania mostró resultados similares.

Los investigadores midieron la calidad de la atención al observar las prescripciones para las enfermedades comunes en los establecimientos de salud (727 observaciones, dos estudios; pruebas muy poco confiables) y al observar las prescripciones realizadas por los trabajadores sanitarios legos (1051 observaciones, tres estudios; pruebas muy poco confiables). No fue posible confirmar un efecto consistente sobre las prescripciones en los establecimientos de salud o por los trabajadores sanitarios legos, ya que las pruebas fueron muy poco confiables.

Para la cobertura con materiales para la AIEPI, se examinó la cobertura con vacunas y vitamina A, la solicitud de atención apropiada y la lactancia materna exclusiva. Dos ensayos (India, Bangladesh) calcularon la cobertura con vacunas contra el sarampión e informaron que probablemente hay poco o ningún efecto sobre la cobertura con la vacuna contra el sarampión (CR 0,92; IC del 95%: 0,80 a 1,05; dos ensayos, 4895 participantes; pruebas de confiabilidad moderada), y en el ECAD de Tanzania se observaron efectos similares. Dos estudios midieron la tercera dosis de la vacuna contra la difteria, la tos ferina y el tétanos; y dos midieron la cobertura con vitamina A; todos proporcionaron pocas o ninguna prueba de un aumento de la cobertura con la AIEPI.

Cuatro estudios (dos de la India y uno de Tanzania y otro de Bangladesh) informaron la solicitud de atención apropiada y obtuvieron información a partir del interrogatorio cuidadoso a las madres acerca de enfermedades recientes. Algunos estudios sobre los efectos de la AIEPI pueden informar mejor sobre el comportamiento de solicitar atención, pero otros no lo informaron.

Los cuatro estudios registraron las respuestas de las madres sobre la lactancia materna exclusiva. Proporcionaron resultados mixtos y pruebas muy poco confiables. Por lo tanto, no se sabe si la AIEPI repercute en la lactancia materna exclusiva.

Ningún estudio informó sobre la satisfacción de las madres y los usuarios de los servicios.

Conclusiones de los autores

Hubo una mezcla variada de intervenciones examinadas en los estudios de investigación que evaluaron la estrategia de AIEPI, y algunos estudios incluyen contribuciones específicas para mejorar la salud neonatal. La mayoría de los estudios se realizaron en el sur de Asia. Implementar la estrategia de atención integrada de las enfermedades prevalentes de la infancia puede reducir la mortalidad en la niñez, y los paquetes que incluyen intervenciones durante el período neonatal pueden reducir la mortalidad infantil. La AIEPI puede tener poco o ningún efecto sobre el estado nutricional y probablemente tiene poco o ningún efecto sobre la cobertura con vacunas. El comportamiento materno de solicitar atención puede ser más apropiado con la AIEPI, pero los resultados de los estudio han sido mixtos y proporcionan pruebas muy poco confiables acerca de si la AIEPI tiene efectos sobre la adherencia a la lactancia materna exclusiva.

PICO

Population
Intervention
Comparison
Outcome

El uso y la enseñanza del modelo PICO están muy extendidos en el ámbito de la atención sanitaria basada en la evidencia para formular preguntas y estrategias de búsqueda y para caracterizar estudios o metanálisis clínicos. PICO son las siglas en inglés de cuatro posibles componentes de una pregunta de investigación: paciente, población o problema; intervención; comparación; desenlace (outcome).

Para saber más sobre el uso del modelo PICO, puede consultar el Manual Cochrane.

Resumen en términos sencillos

Estrategia de atención integrada de las enfermedades prevalentes de la infancia (AIEPI) para los niños menores de cinco años de edad

¿Cuál es el objetivo de esta revisión?

El objetivo de esta revisión Cochrane es evaluar los efectos de los programas que utilizan la estrategia de atención integrada de las enfermedades prevalentes de la infancia (AIEPI) de la Organización Mundial de la Salud. Los investigadores Cochrane buscaron todos los estudios potencialmente relevantes y encontraron cuatro estudios que cumplieron los criterios de la revisión.

Mensajes clave

Esta revisión muestra que el uso de la estrategia de AIEPI de la Organización Mundial de la Salud puede dar lugar a menos muertes entre los niños desde el nacimiento hasta los cinco años de edad. Los efectos de la AIEPI sobre otros aspectos como la enfermedad o la calidad de la atención fueron mixtos, y algunas pruebas fueron muy poco confiables. En el futuro, los investigadores deben estudiar cómo se debe mejorar la administración de la estrategia de AIEPI.

¿Qué se estudió en la revisión?

A nivel global más de 7 500 000 niños mueren cada año antes de alcanzar la edad de cinco años. La mayoría son de comunidades pobres y viven en los países más pobres. Estos niños tienen mayores probabilidades que otros de padecer desnutrición e infecciones como la sepsis neonatal, el sarampión, la diarrea, el paludismo y la neumonía.

Las estrategias efectivas para la prevención y el tratamiento de las enfermedades de los niños están disponibles pero no llegan a ellos. Una razón de lo anterior es que los servicios de asistencia sanitaria a menudo están demasiado lejos o son muy costosos. Los establecimientos de salud en estos contextos a menudo carecen de suministros y trabajadores sanitarios bien adiestrados. Además, los niños enfermos pueden tener varios problemas de salud al mismo tiempo, lo que puede dificultar el diagnóstico y el tratamiento para los trabajadores sanitarios.

En los años noventa, la Organización Mundial de la Salud (OMS) desarrolló una estrategia llamada atención integrada de las enfermedades prevalentes de la infancia (AIEPI) dirigida a estos problemas. Esta estrategia tiene como objetivo evitar la muerte y las enfermedades a la vez que mejora la calidad de la atención a los niños enfermos hasta la edad de cinco años. Consiste en tres partes.

• Mejoría de las habilidades de los trabajadores sanitarios al proporcionar adiestramiento y guías.

• Mejoría en la organización y administración de los sistemas de asistencia sanitaria, que incluye el acceso a los suministros.

• Visitas a los domicilios y a las comunidades para promover buenas prácticas de crianza de los niños y una buena nutrición, a la vez que estimulan a los padres a llevar a sus hijos a un consultorio cundo los niños están enfermos.

La OMS alienta a los países a que adapten la estrategia de AIEPI a sus propios contextos nacionales. Los tipos de enfermedades de la infancia priorizados y las maneras en las cuales se prestan los servicios pueden variar de un país a otro.

¿Cuáles son los principales resultados de la revisión?

Esta revisión Cochrane incluyó cuatro estudios que evaluaron la efectividad de la estrategia de AIEPI. Estos estudios se realizaron en Tanzania, Bangladesh y la India. La estrategia de AIEPI se utilizó de forma muy diferente entre los estudios. Por ejemplo, el estudio de Tanzania implementó el adiestramiento de los trabajadores sanitarios y mejoró el suministro de fármacos, pero no incluyó visitas al domicilio ni actividades comunitarias; el estudio de Bangladesh añadió nuevos trabajadores sanitarios a la vez que adiestró a los trabajadores sanitarios existentes; y los dos estudios indios se dirigieron específicamente a los recién nacidos, así como a los niños mayores.

Esta revisión mostró que el uso de la AIEPI:

• puede dar lugar a menos muertes entre los niños desde el nacimiento hasta los cinco años de edad (pruebas poco confiables);

• puede tener poco o ningún efecto sobre el número de niños que presentan retraso del crecimiento (pruebas poco confiables);

• probablemente tiene poco o ningún efecto sobre el número de niños que presentan emaciación (pruebas de fiabilidad moderada);

• probablemente tiene poco o ningún efecto sobre el número de niños que reciben vacunas contra el sarampión; y

• puede dar lugar a resultados mixtos en el número de padres que solicitan atención cuando su hijo está enfermo.

No se sabe si la AIEPI tiene algún efecto sobre la manera en la que los trabajadores sanitarios tratan las enfermedades comunes porque las pruebas fueron muy poco confiables.

No se sabe si la AIEPI tiene efectos sobre el número de madres que lactan a su hijo de forma exclusiva porque las pruebas fueron muy poco confiables.

Ninguno de los estudios incluidos evaluó la satisfacción de las madres y los usuarios de los servicios al utilizar una estrategia de AIEPI.

¿Cuán actualizada está esta revisión?

Los autores de la revisión buscaron estudios que se habían publicado hasta el 30 junio 2015.

Authors' conclusions

Implications for practice

Providing accessible comprehensive primary health care services to children in low‐ and middle‐income countries seems a good approach to providing health care. This review indicates that IMCI may have a modest effect on mortality and may well be worth implementing, but policymakers need to be careful about justifying the considerable investment on the basis that it will result in large improvements in mortality.

One study measured neonatal and infant mortality and showed that these may be lower in the IMNCI group than in the control group. In this study, the strategy included neonatal care, emphasizing that these services have the potential to create impact during this period when mortality is high. IMCI programmes should consider including services directed at the neonate ("IMCNI") as an integral component of the strategy.

In addition, this strategy, variously implemented in these studies, did not show consistent effects on quality of care, and the certainty of evidence was very low because of concerns regarding precision, consistency, and directness. Therefore we do not know whether IMCI improves quality of care.

There is a continuing need to assure the components of the IMCI package are delivered appropriately, that coverage is maintained and that managerial and support approaches are taken to assure that appropriate, good quality care is in place.

Implications for research

Demonstrating an effect on mortality of effective implementation of routine primary neonatal and child health care services is a large and expensive undertaking. Many influences on child mortality occur over time, and studies must be large. Efforts by researchers to evaluate effects of IMCI help to demonstrate this. In the meantime, services and health may be improving over time, as was clear in Arifeen 2009, which reported dramatic falls in child mortality over the five years of the study in both intervention and control arms.

Important further research will involve evaluating strategies that improve access to, and the quality of, various components of delivery of a comprehensive package of primary child health care, with the IMCI package serving as a base for countries to draw on and modify as appropriate.

Summary of findings

Open in table viewer
Summary of findings for the main comparison. Integrated management of childhood illness strategy compared with routine care

Patient or population: children < 5 years of age

Settings: middle‐ and low‐income countries

Intervention: integrated management of childhood illness

Comparison: usual health services

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

IMCI

Mortality

Child mortality

Risk ratio 0.87a

(0.68 to 1.10)

5090 children

(1 trial)1

⊕⊕⊝⊝

Lowb,c

due to indirectness and imprecision

Child mortality may be decreased, but confidence intervals include no effect

31 per 1000 live births

27 per 1000 live births
(21 to 34)

Infant mortality

HR 0.85

(0.77 to 0.94)

60,480e

(1 trial) 2

⊕⊕⊝⊝
Lowf,g,h

due to indirectness and imprecision

Infant mortality may decrease

69 per 1000 live births

59 per 1000 live births

(54 to 65)d

Nutritional status

Stunting

Risk ratio 0.94i

(0.84 to 1.06)

5242

(2 trials) 1,2

⊕⊕⊝⊝
Lowb,f,j

due to indirectness and imprecision

Little or no effect on stunting possible

57 per 100

53 per 100

(48 to 60)

Wasting

Risk ratio 1.04i

(0.87 to 1.25)

4288

(2 trials) 1,2

⊕⊕⊕⊝
Moderateb,j

due to indirectness

Probably little or no effect on wasting

13 per 100

14 per 100

(11 to 16)

Quality of care

Prescribing at health facilities

Mixed effectsk

727

(2 studies)1,3

⊕⊝⊝⊝

Very lowl,m

due to imprecision, inconsistency, and indirectness

Not known whether consistent effect on prescribing quality at health facilities

Prescribing by lay health care workers

No consistent effects

1051 observations

(3 studies)1,3,4

⊕⊝⊝⊝

Very lowl,m

due to imprecision, inconsistency, and indirectness

Not known whether consistent effect on prescribing quality of lay health care workers

Coverage of IMCI deliverables

Vaccine coverage (measles)

RR 0.92

(0.80 to 1.05)

4895

(2 trials) 1,2

⊕⊕⊕⊝

Moderaten,j

due to indirectness

Probably little or no effect on measles vaccine coveragen

57/100

54/100

(46 to 60)

Supplement coverage (vit A)

RR 0.93

(0.88 to 0.98)

831

(1 trial)1

⊕⊕⊕⊝

moderaten,j

due to indirectness

Probably little or no effect on vitamin A coverage

83 per 100

77 per 100

(73 to 81)

Appropriate care seeking

Mixed effectso

4182

(3 studies)1,2,3

⊕⊕⊝⊝
Lowp

due to inconsistency

Appropriate care seeking possibly improved in some studies, but not in others

Exclusive breast feeding

Mixed effectsq

7975

(4 studies) 1,2,3,4

⊕⊝⊝⊝
Very lowp,r,s,t,u

due to indirectness and inconsistency

Not known whether effect on exclusive breast feeding

Satisfaction of beneficiaries

Not measured

Not known whether users prefer IMCI or usual clinics

The basis for assumed risk is median control group risk across studies. The corresponding risk (and its 95% confidence interval) is based on assumed risk in the comparison group and relative effect of the intervention (and its 95% CI)
CI: confidence interval; ICC: intracluster correlation co‐efficient; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: We are very confident that the true effect lies close to the estimate of effect
Moderate certainty: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of effect but may be substantially different
Low certainty: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of effect
Very low certainty: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect.

aIn the Bangladesh trial, mortality declined over the 5 years from 43 per 1000 live births to 27 per 1000 live births in the intervention area (reduced by 37%), and from 44.8 per 1000 live births to 31.2 per 1000 live births in control areas (reduced by 30%). A small difference in the reduction in child mortality was noted in the 2 groups (8.6% in the intervention group vs 7.8% in control groups).

The Tanzanzia CBA study had mortality estimates that were very similar to the Bangladesh trial (RR 0.87, 95%CI 0.72 to 1.05).

bDowngraded by 1 for serious indirectness: The Bangladesh trial modified the intervention after early analysis for care seeking and referral completion, suggesting that coverage was not increasing as expected. This included modification of treatment and referral guidelines and introduction of a new cadre of village health care workers trained and equipped to provide community case management for pneumonia and diarrhoea in 2005. These adjustments, including the new staff cadre, were in response to an intermediate process evaluation in the trial, and are unlikely to be mirrored in routine implementation programmes.

cDowngraded by 1 for imprecision: 95% CI is wide and includes a clinically important reduction in mortality and no effect. In addition, dominant change was secular (see note 1)

dAbsolute rates were calculated from hazard ratio by using the formula RR = (1 ‐ exp(HR ×ln(1 ‐ assumed risk)))/assumed risk

eIMCI in this trial included perinatal and neonatal components

fDowngraded for serious imprecision. Confidence intervals include no important effect to an important effect

gDowngraded by 1 for serious indirectness: This single study was conducted in a mixed rural/urban population in northern India with a substantive neonatal component with home visiting. Findings may not be easily generalized to other settings in Asia or elsewhere

hSubgroup analysis showed lower mortality in the intervention group among babies delivered at home, with no effect apparent in the subgroup delivering at hospital. This subgroup effect was evident for both neonatal and infant mortality

iConfidence intervals for Arifeen adjusted assuming ICC of 0.01

j The Tanzania CBA study has very similar estimates compatible with this estimate

kLarge improvements in 6 parameters in Arifeen; no clear effect in 2 parameters in Schellenberg

lDowngraded by 1 for both imprecision and inconsistency. Small numbers of participants observed; effect varies between trials and parameters measured

mDowngraded by 1 for indirectness. All measurements through direct observation of health care worker; may not represent behavior unobserved

nDowngraded by 1 for indirectness. Approximately 80% of the estimate taken from 1 study, so generalisability to other settings is uncertain

oPoint estimate for vaccine coverage suggests higher coverage in control group, and 95% confidence intervals exclude beneficial effect of IMCI on coverage.

pThis outcome was measured in various ways by different studies on samples of patients. Large improvements noted in some studies but not in others. As the outcome was so varied, we did not prepare a meta‐analysis

qDowngraded by 2 for inconsistency. Some large effects in some studies, and modest/no effects in others

rMixed effects between the 4 studies preclude meta‐analysis

sDowngraded by 2 for inconsistency. Large amounts of qualitative heterogeneity

tDowngraded by 1 for indirectness. See (b) above and the large effects seen in Bhandari associated with several home visits, which would not be feasible in other settings

uDowngraded by 1 for risk of bias. Breast feeding was reported through questionnaire from health care workers to mothers

Studies

1 Arifeen 2009;2 Bhandari 2012; 3 Schellenberg 2004 ; 4 Mohan 2011

Background

Description of the condition

More than 7.5 million children globally die each year before reaching the age of five. Most of these deaths occur in low‐ and middle‐income countries (LMICs) (Black 2003; Liu 2012), where interaction of common infections (including neonatal sepsis, measles, diarrhoea, malaria, and pneumonia) with poor nutritional status, combined with inadequate health infrastructure and poverty, results in poor health outcomes (Liu 2012; Tulloch 1999). Statistical projections over the past decade suggest that these common childhood illnesses will continue to be major contributors to the child morbidity and mortality burden until 2020 (Murray 1996). These projections have been uncannily accurate, as shown by recent mortality data (WHO 2012), providing a strong case for introducing new strategies to tackle problems contributing to poor outcomes.

In addition to overall high child mortality globally, there are large differences in mortality between countries, with earlier studies indicating that 95% of global mortality happens in 42 less‐developed countries (Victora 2003); there are also differences in mortality between socio‐economic groups within countries. Children who belong to the more underprivileged sections of society are more likely to suffer from malnutrition and to experience greater severity of illness and higher mortality (Black 2003; Victora 2003). These inequalities are reflected in the quality of health care received. Studies have shown that at first‐level health facilities in LMICs, assessment by health care workers is poor, treatment facilities are inadequate, and parents receive improper advice (Barros 2012; World Health Organization 1998).

Providing quality care to sick children in LMICs is important. Effective and affordable interventions have been known to reduce childhood morbidity and mortality for some time, but their availability, accessibility, and acceptability to the ultimate beneficiaries have been unacceptably low (Bryce 2003; Jones 2003).

Description of the intervention

Individual health interventions shown to be effective in reducing child mortality include exclusive breast feeding, improved vaccination coverage, oral rehydration therapy, pneumonia therapy, and early treatment for malaria in endemic areas (Bhutta 2008; Markowitz 1991; Mathew 2011; Thwing 2011). However, children presenting to first‐level health facilities seldom present with a single ailment. The presence of multiple and overlapping morbidities makes diagnosis and treatment difficult for the health care worker. Although each of these interventions has been individually shown to be effective, it has gradually become clear to health care planners that a more integrated approach is needed to achieve better outcomes. This has resulted in a policy push toward a multi‐pronged strategy aimed at integrating improved health care services with better case management skills and healthier community practices to reduce child mortality and morbidity (WHO 1996). Health care packages that aim to integrate these components of health care strategy have been designed and implemented at community, national, and international levels. In the mid‐1990s, the World Health Organization (WHO), in collaboration with the United Nations Children's Emergency Fund (UNICEF) and other agencies, developed a strategy known as integrated management of childhood illness (IMCI) in response to these challenges.

The IMCI strategy includes both curative and preventive interventions targeted at improving health practices at health care facilities, at home, and in the community. This strategy includes three main components (Tulloch 1999): (1) improvement in the case management skills of health care staff through provision of locally adapted guidelines on IMCI and activities to promote their use; (2) improvement in the overall health care system required for effective management of childhood illnesses; and (3) improvement in family and community health care practices.

In 1995, WHO technical programs and partners, supported by sound research, introduced case management guidelines for IMCI (WHO 1997), with a core intervention targeting five of the most important causes of child mortality: acute respiratory infection (ARI), diarrhoea, measles, malaria, and malnutrition. The following year, a training program was targeted at first‐level health care workers. These case management guidelines were adapted to local epidemiology and clinical practice, and training of the first health care workers started in 1995. This was followed by a short period of exploratory implementation and documentation in a small number of countries (Lambrechts 1999). After an initial pilot phase, IMCI was introduced in Tanzania and Uganda in 1996 (Bryce 2005). Results from these two countries were encouraging, with improvements noted in quality of care and health care worker practices (Lambrechts 1999). In the early phase of its implementation, IMCI was focused on training health care workers, with less attention paid to the other two components, namely, strengthening health care systems and improving community practices. Initial guidelines and training materials were considered appropriate for countries with an infant mortality rate greater than 40/1000 live births, and with documented transmission of Plasmodium falciparum malaria. The guidelines and training materials represented an attempt to outline what needed to be done at a first‐level health facility by any health worker ‐ doctor, nurse, or paramedical worker ‐ seeking to treat sick children while reducing mortality.

Upon receipt of an encouraging response from partner organizations, various countries, and the World Bank, the WHO provided a detailed blueprint of a three‐phase rollout for countries wishing to adopt IMCI (WHO 1999). The process consisted of the introduction phase, the early implementation phase, and the expansion phase. The purpose of the introduction phase is to ensure that policymakers understand IMCI. This involves initiating contact to provide information, holding orientation meetings, and building national capacity in IMCI. In the early implementation phase, health care staff conduct and monitor IMCI activities in a limited number of districts to study impact. Other issues studied during this phase include the relationship of IMCI to other health care sector activities, drug availability, and policy and supervision. The expansion phase involves increasing access to interventions introduced in the first two stages. The WHO and collaborating agencies provide technical assistance in preparation for early implementation of IMCI.

Anecdotal data, qualitative reviews, and systematic reviews from various countries suggest that IMCI has been effective in improving health service quality and increasing health care cost savings (Ahmad 2010; Amaral 2008). Since its introduction, IMCI has been taken up by numerous countries, initially as a pilot project, and later as a national program. The three components of IMCI have been implemented in various ways in different countries. Key features of IMCI include its evidence‐based approach to diagnosis and treatment and its flexibility in terms of adapting guidelines to local epidemiological situations. The adaptation process involves detailed comparisons of existing guidelines in a country with IMCI and application of the most effective components of both. Consensus is needed on the conditions that should be covered. Malaria can be removed from guidelines in which falciparum malaria is not a problem. Other countries have included dengue fever as an important problem. IMCI has already been adapted to include the neonatal period, and some countries, like India, have incorporated neonatal care in implementation of the program. Selection of antibiotics for ARI and diarrhoea is based on local sensitivity patterns and availability. Some countries have shortened the duration of training to reduce costs. In many countries, especially in sub‐Saharan Africa, HIV/AIDS contributes significantly to child morbidity and mortality, resulting in the need to include specific assessment and management of symptomatic HIV infection in IMCI guidelines. A draft HIV component of the IMCI guidelines, which included management of symptomatic HIV cases with referral for counselling and testing, was evaluated in South Africa. A revised version was then validated in Ethiopia and Uganda, where prevalence of HIV, malnutrition, and malaria is different from South Africa. IMCI materials were then adapted to include an HIV component (Qazi 2006). The WHO has formulated an Adaptation Guide to describe the process of adaptation by a country and facilitate continuous evolution of the program (WHO 1999a).

Large‐scale rollout and continuation of IMCI require money. In several countries, external donors have largely funded IMCI implementation. Within 10 years, donor support began to wane, leaving health departments of poor countries with inadequate funds (Duke 2009). Indeed the places where IMCI is needed most, and in which it provides the greatest impact, are those in which the health care system is weakest and implementation of the strategy often fades. Therefore, it is important to ensure adequate development along with the introduction of newer innovations. A global study conducted across 27 countries cited high cost as a major challenge to scaling up of the program (Goga 2011). Apart from modifications such as shortening of training duration, new technology such as the IMCI computerized adaptation and training tool (ICATT) is being introduced. Trials are currently under way to assess the effectiveness of these tools.

How the intervention might work

The IMCI clinical guidelines target children up to five years of age ‐ the age group that bears the greatest burden of death from common childhood diseases. These guidelines are derived from an evidence‐based, syndromic approach to case management and emphasize rational, effective, and affordable use of drugs and diagnostic tools (Gove 1997; Hill 2004). With well‐formulated guidelines and proper training of health care workers, it would be possible to systematically assess common symptoms and clinical signs, ultimately leading to rational and effective actions. Such an approach can help in diagnosing the clinical condition, assessing the severity of the condition, and implementing actions that can be taken to care for the child (e.g. refer the child immediately, manage within available resources, manage at home).

Initially, IMCI referred to case management of children. It later became a vehicle for WHO and UNICEF child survival strategies at household, community, health facility, and referral levels. Thus it incorporated health service strengthening on the one hand and, on the other hand, face‐to‐face nutrition and health advice provided through home visits and active involvement of family members and the community in the health care process (Gove 1997; Hill 2004). Thus, over the years, implementation of IMCI, called the IMCI strategy, has come to include three components.

  • Training component: training of health care workers in clinical care with the use of IMCI guidelines.

  • Systems component: investment in health care systems organization and management, including supplies, related specifically to delivery of IMCI.

  • Community health component: Auxiliary health care staff and community health care workers attached to clinics conduct home visits and community health promotion to promote good child rearing practices, good nutrition, and access to services when the child is ill (Hill 2004).

Why it is important to do this review

Currently, more than 75 countries are implementing the IMCI strategy on a large scale. For years, individual aspects of child health, often contained within trials evaluating the efficacy of one intervention, have been carried out, for example, in vitamin A supplementation. Individual components of IMCI have often been tested and have proved effective in rigorously conducted randomised controlled trials and systematic reviews. However, it is unclear whether delivery of this package impacts hard outcomes such as mortality. As provision of IMCI is expensive, solid evidence of an impact on child health contributes to continued provision of political and financial support of this comprehensive child health strategy.

Global evaluation of IMCI, called "the multi‐country evaluation of IMCI," was started in the early 1990s to generate information on effectiveness, cost, and impact, alongside other initiatives, such as the IMCI evaluation by the Centers for Disease Control and Prevention (CDC) (Schellenberg 2004); investigators reported across five study sites (WHO 2002). Other reviews have described health care worker performance as the primary outcome indicator (Amaral 2008) or have assessed the impact of the duration of training for IMCI (Rowe 2008), thereby not analysing the impact of the intervention on beneficiaries. A comprehensive systematic review is therefore required to evaluate the effectiveness of IMCI in improving child health (as measured by mortality or nutritional status), its impact on the quality of care delivered, and whether basic healthy practices delivered by caregivers improve.

Objectives

To evaluate the effects of programs that implement the integrated management of childhood illnesses (IMCI) strategy in terms of death, nutritional status, quality of care, coverage with IMCI deliverables, and satisfaction of beneficiaries.

Methods

Criteria for considering studies for this review

Types of studies

Randomised controlled trials, including cluster‐randomised trials.

Non‐randomised trials with a concurrent comparison group (no IMCI intervention) and adjustment for baseline characteristics and confounders.

Controlled before‐after (CBA) studies in which allocation to different comparison groups was not made by study investigators, and outcomes were measured in both intervention and control groups at baseline and after the IMCI program had been introduced.

All studies required at least two intervention sites and at least two control sites.

Types of participants

The unit of study was primary health care services in low‐ and middle‐income countries (as categorized by The World Bank using gross national income per capita in US dollars and the Atlas conversion factor (World Bank 2012)). This could be provided by the public, private, or non‐government agency sector.

Participants were children younger than five years of age and health care providers in low‐ and middle‐income countries (as categorized by The World Bank using gross national income per capita in US dollars and the Atlas conversion factor (World Bank 2012)).

Types of interventions

Children younger than five years of age allocated to receive the generic WHO/UNICEF IMCI intervention or its adaptation. To be included, the IMCI intervention needed to include improving health care worker skills for case management as one component.

We included studies of (1) IMCI training alone; (2) IMCI training plus systems interventions to improve care delivery; (3) IMCI training with additional activities to improve community health practices; and (4) all three interventions.

We excluded studies that included IMCI only as a part of a wider intervention package that could include conditional cash transfers, food supplementation, employment, and vertical disease‐specific measures.

Studies providing specific additional interventions in both intervention and control areas were eligible for inclusion as long as these additional interventions were similar across intervention and control areas.

Comparison

We included studies in which the comparison group received usual health services without the integrated health care package (IMCI).

Types of outcome measures

  • Measures of mortality (neonatal, infant, and under‐five mortality) rates.

  • Measures of nutritional status, including stunting and wasting.

  • Quality of care assessed by adherence to standard practice guidelines.

  • Coverage of key IMCI deliverables, including (1) vaccine coverage; (2) appropriate care seeking for common illnesses; and (3) exclusive breast feeding.

  • Satisfaction of beneficiaries.

As one study also reported on other newborn care practices, which we did not anticipate, we describe these results under "coverage." In addition, in the protocol, we stated that we would assess morbidity episodes as secondary outcomes. As it is unlikely that IMCI would influence the incidence of disease, and studies did not report on this, we have not commented further on this outcome.

Search methods for identification of studies

Electronic searches

We attempted to identify all relevant trials irrespective of language or publication status. We used the search term "IMCI" OR "IMNCI" OR "integrated management of childhood illness" across various databases. A more complex search strategy was not needed, as "IMCI" does not have a corresponding medical subject heading (MeSH) term, and all papers that consider IMCI use this term in the title, abstract, or text.

We (TG and DS) searched the following databases using the strategy described above.

  • Cochrane Central Register of Controlled Trials (CENTRAL) (www.cochranelibrary.com), including the Cochrane Effective Practice and Organisation of Care (EPOC) Group Specialised Register (searched 30 June 2015).

  • MEDLINE (1946 to date), Ovid (searched 30 June 2015).

  • EMBASE (1980 to date), Ovid (searched 30 June 2015).

  • Cumulative Index to Nursing and Allied Health Literature (CINAHL) Plus (2000 to date), EbscoHost (searched 30 June 2015).

  • Latin American Caribbean Health Sciences Literature (LILACS), Virtual Health Library (VHL) (searched 30 June 2015).

  • World Health Organization (WHO) Library & Information Networks for Knowledge Database (WHOLIS) (searched 30 June 2015).

  • Science Citation Index and Social Sciences Citation Index, Institute for Scientific Information (ISI) Web of Science (1950 to present) (searched 30 June 2015).

  • Population Information Online (POPLINE) (searched 30 June 2015).

  • World Health Organization (WHO) International Clinical Trials Registry Platform (WHO ICTRP) (searched 30 June 2015).

  • Global Health (1973 to 2016 Week 17), OvidSP (searched 08 May 2016).

  • Health Management (1986 to present), ProQuest (searched to 17 December 2012. We did not have access to this database after this date).

We have listed in Appendix 1 search strategies used for the various databases and the number of trials identified.

Searching other resources

We scanned the reference lists of all included papers and relevant reviews to identify citations that could have been missed in the primary search. We contacted authors of other relevant reviews in the field regarding relevant studies of which they were aware.

Data collection and analysis

Selection of studies

Two review authors (TG and DS) removed duplicate records, then independently scanned the titles and abstracts of studies identified in the computerized search to exclude literature that clearly did not meet the inclusion criteria. We examined full‐text articles against eligibility criteria while using a structured form. We resolved uncertainties about inclusion by discussion and consensus between all review authors. Controlled before‐after studies were required to include at least two control groups and at least two intervention groups, as otherwise differences detected are totally confounded by study site.

Data extraction and management

Two review authors (TG and DS) used a structured form to independently extract relevant data, including details of methods, participants, setting, context, interventions, outcomes and results, publications, and investigators. We resolved discrepancies by mutual discussion. When discrepancies could not be resolved, we sought assistance from a third review authors (HSS).

We described the IMCI strategy by using a matrix to detail inputs and activities. This matrix includes (1) training inputs; (2) tools and manuals, including guidelines; (3) additional equipment and drugs provided; (4) managerial supervision and monitoring, including additional health information collected; and (5) engagement, training, and support of community volunteers, as well as health care providers involved in the program. We intended to stratify the analysis to reflect inputs (separating simple training; training and systems support; training and community engagement; and training, systems support, and community engagement) but found that data were insufficient.

Assessment of risk of bias in included studies

Two review authors (TG and DS) independently assessed the risk of bias for each controlled trial and controlled before‐after study using criteria outlined in the Cochrane Handbook for Systematic Reviews of Interventions and those recommended by EPOC (EPOC 2015; Higgins 2011). For randomised controlled trials, non‐randomised controlled trials, and CBA studies, these criteria include the following.

  • Sequence generation (selection bias).

  • Allocation sequence concealment (selection bias). 

  • Blinding of participants and personnel (performance bias).

  • Blinding of outcome assessment (detection bias).

  • Incomplete outcome data (attrition bias).

  • Selective outcome reporting (reporting bias).

  • Comparability of baseline outcome and characteristics.

  • Protection from contamination.

  • Other potential sources of bias.

For cluster‐randomised trials, particular biases to consider include the following.

  • Recruitment bias.

  • Baseline imbalance.

  • Loss of clusters.

  • Incorrect analysis.

We omitted "comparability with individually randomised trials", as this intervention could be tested only in the context of a cluster trial (Higgins 2011).

The judgment for each entry involves assessing risk of bias as "low," "high," or "unclear," with the last category indicating lack of information or uncertainty over the potential for bias. We resolved disagreements by discussion between review authors.

Measures of treatment effect

We expressed results as risk ratios (RRs) with 95% confidence intervals (CIs) for binary outcomes. We analysed continuous outcomes using mean differences (MDs).

Unit of analysis issues

When a cluster‐randomised trial was adjusted for clustering, we extracted cluster‐adjusted results and used them in analyses.

When a cluster‐randomised trial did not adjust for clustering, we extracted unadjusted results. As we were not able to obtain an estimate of intracluster correlation co‐efficients (ICCs) from the trials themselves, we used sensitivity analyses and an estimated ICC of 0.01 to investigate the impact of clustering on estimates of effectiveness.

Dealing with missing data

We anticipated that we would need to impute values to estimate cluster effects, but this was not required.

Assessment of heterogeneity

We described the context in which the intervention was implemented. We described in the table of included studies variability among participants, interventions, and outcomes studied.

Statistical heterogeneity was to be identified and measured as recommended by the Cochrane Handbook for Systematic Reviews of Interventions (Section 9.5.2) (Higgins 2011). As we found so few studies, we were careful about conducting meta‐analysis and carried this out only when it made sense to do so. If heterogeneity based on Chi2 was assessed as greater than 50%, we used a random‐effects model and interpreted results carefully.

Assessment of reporting biases

We anticipated using funnel plots to examine for publication bias but found insufficient trials to do this.

Data synthesis

Overall, the review provides a structured synthesis. When meta‐analysis made sense, we used Review Manager software (RevMan 5.3), expressing results as risk ratios with 95% confidence intervals, or mean differences, as applicable. We used CBA results alongside the trials results, but did not combine them statistically. We assessed the certainty of the evidence by using the GRADE approach and summarized key findings in summary of findings Table for the main comparison.

Subgroup analysis and investigation of heterogeneity

Our planned subgroup analyses were not possible, as data were insufficient.

Results

Description of studies

Results of the search

Searches of various databases yielded 1499 records to be screened, after duplicates were deleted. Of these, we found 1433 irrelevant to the review on screening. We obtained full texts of the remaining 50 studies, reported in 66 publications. Of these, four studies (two cluster RCTs and two CBA studies) described in 12 articles met our inclusion criteria (Figure 1). We reported reasons for excluding studies in the Characteristics of excluded studies table. We identified one trial through other sources in May 2016 (Boone 2016). We included this study amongst Studies awaiting classification and will consider it in an update in due course.


Study flow diagram.

Study flow diagram.

Included studies

Locations and populations

Studies were conducted in Tanzania (data collection from 1997 to 2002), Bangladesh (1999 to 2007), and India (2006 to 2010). One analysis was obtained from India's national program (2005 to 2009).

Schellenberg 2004 was carried out in four rural districts of Tanzania, with two intervention clusters and two control clusters that were geographically contiguous and matched for mortality rates. Arifeen 2009 was conducted in Bangladesh, in areas of a subdistrict where the sampling frame consisted of first‐level outpatient facilities. Bhandari 2012 was carried out in primary care health centres within a single district of a state in Haryana, India. In a second study from India, Mohan 2011 collected data from 12 districts of India that had initiated IMCI and compared them with data from matched control districts.

Strategies

Interventions are summarized as an input matrix (Table 1) related to human resource policies, health systems strengthening, and strategies for community engagement. Trials varied substantially in range of inputs provided. The earliest trial comprised two IMCI components: training for basic health care workers, and drug supply combined with tools and manuals (Schellenberg 2004).

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Table 1. IMCI components

Schellenberg 2004

Arifeen 2009

Mohan 2011

Bhandari 2012

Human resources policies for health care professionals

IMCI training

Basic health care worker

Y

Y

Y

Y

Senior/other

Y

Y

Doctors

Y

TBA

Y

Refresher

Private sector

Y

Staff recruitment

Filling vacancies

Y

New cadre of community health care worker (CHW)

Y

Conditions of service

Cash incentives

Y

Management

Home visits

Y

Y

Y

Supervision and monitoring

Y

Y

Y

Health system strengthening

Tools and manuals including guidelines

Supply education materials

Y

Y

Additional equipment and drugs

Drug supply

Ya

Y

Y

Y

Supply minor equipment

Y

Strategies for community engagement

Training

Unqualified village doctors

Y

Y

Social development

Establishing mother/women group meetings

Y

Y

Support of community leaders/volunteers

Y

Community theatre

Y

IMCI: integrated management of childhood illness; TBA: traditional birth attendant

aAssumed, as the study is an assessment of first 2 components of World Health Organization (WHO) generic integrated management of childhood illness (IMCI)

Arifeen 2009 included training of basic health care workers but provided more substantive supervision, health service strengthening, and strategies for community engagement. Investigators added a new cadre of health worker halfway into the study for treatment of community pneumonia and diarrhoea.

Bhandari 2012 included training of all cadres of health care workers consisting of human resource management strategies, drug supply, and community engagement, including support to village doctors, women's groups, and women's leaders.

Mohan 2011 reported fewer inputs than Bhandari 2012 but included home visits and drug supply.

The two trials in India (Bhandari 2012; Mohan 2011) modified the IMCI package to include a series of interventions specifically targeted at the neonate. These interventions were defined in the IMNCI guidelines by the Government of India (WHO 1998; WHO 2003).

Details of the interventions are included in Table 2. Routine health care was used for comparison in all trials.

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Table 2. Details of inputs described narratively

Study

Input

Schellenberg 2004

Incorporated 2 components of integrated management of childhood illness (IMCI), namely, training of health care workers and health system strengthening. All health care workers at the primary level received 11 days of training. IMCI nutrition education and counselling cards for educating mothers were prepared after operational research and subsequently translated into Swahili language to improve community practices. Health systems were strengthened using IMCI processes and by providing financial resources of approximately $0.92 per capita to implementing districts

Arifeen 2009

Incorporated all 3 components of IMCI. Health care workers were trained using the 11‐day course, followed by a 3‐day course on breast feeding counselling. Health systems strengthening consisted of making additional drugs available in the intervention area, and setting up a facility‐level drug tracking and reporting system. Job aids such as weighing scales, timer to count respiratory rate, thermometers, chart booklets, and locally adapted cards as aids for counselling mothers were provided to all intervention clusters. To improve community practices, special emphasis was given to messages related to pneumonia and malnutrition and to 3 practice areas, namely, care seeking for sick children, home management of illness, and responsive feeding

Mohan 2011

Retrospectively collected data about IMCI implementation from 12 districts that started implementation in 2005. Details of the intervention have not been described specifically for these 12 districts but are available for the entire country as part of a standard guideline. Training consisted of the 8‐day course for community‐based workers and auxiliary nurse midwives and an additional 2 days for supervisors. Workers are supposed to receive basic drugs and supplies as per guidelines of the Reproductive and Child Health II and Integrated Child Development Scheme (ICDS) programs. Community health practices include home visits to all newborns during which health care workers ensure exclusive breast feeding, provide counsel on temperature maintenance, explain danger signs, assess newborns (and other sick children) and refer them to an appropriate health facility, if required

Bhandari 2012

Health care workers were trained with the 8‐day IMNCI Basic Health Worker Course, and specialists received the 11‐day IMNCI Course for Physicians. Health systems interventions included (1) strengthened supervision of community health care workers and nurses and filling of vacant supervisor positions; (2) task‐based incentives to include IMNCI activities; and (3) establishment of drug depots in villages to ensure regular supply of drugs. Community health care workers made scheduled post‐natal home visits, promoted breast feeding, delayed bathing, provided cord care, and responded to care seeking for illness. They also ran women's health group meetings to increase awareness of healthy newborn care practices

Study design

Two studies were cluster‐randomised trials (Arifeen 2009; Bhandari 2012); two were controlled before‐after studies (Mohan 2011; Schellenberg 2004). Both cluster RCTs used appropriate methods to take clustering into account when reporting measures of treatment effect.

Outcomes

Arifeen 2009 reported mortality in children younger than five years of age, while excluding death in the first week of life. Schellenberg 2004 reported under‐five mortality rates at baseline and at two years after implementation of IMCI. Bhandari 2012 reported neonatal mortality, neonatal mortality beyond the first 24 hours of birth, and infant mortality.

In Arifeen 2009, in the abstract of the article but not in the main text, study authors reported on the percentage difference in mortality rates in the last two years of the study (27.0/1000 in the IMCI group, 31.2/1000 in the control group). This is not corrected for baseline (which is lower in the IMCI group), thus this estimate is inflated. We calculated absolute differences in death between the two groups in summary of findings Table for the main comparison, as these data are more informative.

For nutritional status, three studies reported wasting and stunting (Arifeen 2009; Bhandari 2012; Schellenberg 2004).

For quality of care, Arifeen 2009 reported on health facility readiness and quality of assessment and treatment of sick children.

For coverage of key IMCI deliverables, studies included the following.

No study reported satisfaction of mothers and service users.

Funding

Arifeen 2009 and Schellenberg 2004 were included in the Multi‐Country Evaluation of IMCI Effectiveness, Cost, and Impact (MCE), which was co‐ordinated by the Department of Child and Adolescent Health and Development of WHO. The World Health Organization funded Bhandari 2012. No source of funding was given for Mohan 2011, but three study authors were (at the time of publication) affiliated with WHO or UNICEF.

Excluded studies

The Characteristics of excluded studies table summarizes the reasons why studies were excluded. Of the 45 studies (53 reported papers):

Risk of bias in included studies

See Figure 2 and Figure 3 for summaries of risk of bias, and the Characteristics of included studies table for details of risk of bias and methods used in each trial. Arifeen changed the intervention when care seeking and referral completion did not turn out as expected. This impacted the indirectness and generalisability of the trial.


Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.


Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Effects of interventions

See: Summary of findings for the main comparison Integrated management of childhood illness strategy compared with routine care

Mortality

Three studies summarized in Table 3 reported effects of IMCI on mortality.

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Table 3. Results: mortality

Outcome

Trial ID

Study design

Pre‐intervention mortality rate

Post‐intervention mortality rate

Cluster‐adjusted relative effect
(95% CI)

Coverage indicators

analysis summary

IMCI

Control

IMCI

Control

Neonatal mortality

Bhandari 2012a

Cluster RCT

32.6/1000 live births

(n NA)

32.4/1000 live births

(n NA)

41.9/1000 live births

(1244/29,667)

43/1000 live births

(1326/30,813)

Hazard ratio 0.91b,c

(0.80 to 1.03)

Adjusted for confounders

Infant mortality

Bhandari 2012

Cluster RCT

44.9/1000 live births

(n NA)

43.9/1000 live births

(n NA)

65 per 1000 live births

(1925/29,667)

69 per 1000 live births

(2136/30,813)

Hazard ratio 0.85b
(0.77 to 0.94)

Adjusted for confounders

Child mortality

Arifeen 2009d

Cluster RCT

43.0 per 1000 live births

(144/3348)

44.8 per 1000 live births
(179/3996)

27.0 per 1000 live births

(157/5815)

31.2 per 1000 live births

(221/7083)

Risk ratio 0.87

(0.66 to 1.14)

No effect after exclusion of injuriese

Schellenberg 2004f

CBA

27.2 per 1000 child‐years

(639/23,515)

27.0 per 1000 child‐years

(242/8977)

24.4 per 1000 child‐years

(1220/49,964)

28.2 per 1000 years

(619/21,965)

Risk ratio 0.87

(0.72 to 1.05)

No effect after adjustment

CBA: controlled before‐after study; IMCI: integrated management of childhood illness; RCT: randomised controlled trial
aBhandari 2012: Fieldworkers not involved with IMNCI implementation visited households monthly to identify new pregnancies. Infants were visited at 1, 3, 6, 9, and 12 months to determine survival

bBhandari 2012: Hazard ratio was calculated after adjustment for cluster design and potential confounders between groups (markers of poverty, literacy, access to services)

cBhandari 2012: Although the overall effect was not statistically significant, a subgroup analysis found that a statistically significant reduction in neonatal mortality was significantly lower in the subgroup born at home (adjusted HR 0.80, 95% CI 0.68 to 0.93)

dArifeen conducted a household census in 2000 and 2007 where the complete birth history of all ever married women between the age of 15 and 49 years was used to estimate yearly and 2 year mortality rates. The data pertains to mortality between day 7 and 5 years of life.

eAfter exclusion of deaths due to malformation and injury (causes not related to IMCI), no effect of IMCI was noted on mortality (data not available)

fThis is the value adjusted for baseline differences in mortality. Unadjusted value is 4.2/1000 fewer deaths (95% CI ‐4.1 to 12.4). Mortality was slightly higher in the control group at baseline. Schellenberg study (Schellenberg 2004)

Also estimated mortality difference after “ignoring the between district variation” as 13% lower mortality (95% CI 5% to 21% lower) (P value = 0.004); risk ratio 0.87 (95% CI 0.79 to 0.95)

Child mortality

One trial and one CBA evaluated this. The Bangladesh trial estimated that child mortality may be 13% lower in the IMCI group, but the confidence intervals include no effect (RR 0.87, 95% CI 0.68 to 1.10, 5090 participants, low‐certainty evidence). The Tanzania CBA study produced very similar estimates (RR 0.87, 95% CI 0.72 to 1.05). (Analysis 1.1).

In the Bangladesh trial, it is important to note that mortality in both intervention and control groups fell markedly over the six‐year period. When the first two years were compared with the last two years, the rate fell from 70.0 to 49.3/1000 live births in the IMCI group, and from 65.6 to 50.5/1000 live births in the control group, but investigators detected no differences between intervention and control groups. Study authors reported that IMCI group mortality was slightly lower by 3.3% (95% CI ‐3.4 to 10.0, adjusted for baseline imbalance), but the estimate includes a null effect (Arifeen 2009).

Infant and neonatal mortality

Bhandari 2012, who included a neonatal component to IMCI, reported data on these outcomes, adjusted for potential confounders (Table 3). The infant mortality hazard ratio (HR) suggests that infant mortality may be lower in the IMNCI group than in the control group (cluster‐adjusted HR 0.85, 95% CI 0.77 to 0.94; low certainty of evidence; Analysis 1.1), although neonatal effects were marginal and confidence intervals included no effect (cluster‐adjusted HR 0.91, 95% CI 0.80 to 1.03; Analysis 1.1). In a subgroup analysis, the neonatal mortality rate was lower in IMCI clusters in the subgroup delivered at home (cluster‐adjusted HR 0.80,95% CI 0.68 to 0.93) but not in those delivered at a health facility (cluster‐adjusted HR 1.06, 95% CI 0.91 to 1.23). This subgroup effect was preserved for infant mortality (home deliveries, cluster‐adjusted HR 0.77, 95% CI 0.69 to 0.87; facility‐based deliveries, cluster‐adjusted HR 0.98, 95% CI 0.87 to 1.10). Study authors attributed the difference in mortality to more effective change in newborn care practices (including early breast feeding, exclusive breast feeding, delayed bathing, appropriate cord care) among home born babies compared with those delivered at the facility. The intervention may have improved timely seeking of health care for sick newborns, thereby affecting neonatal and infant mortality.

In a subsidiary analysis, we examined mortality among participants younger than five years of age, conducting a meta‐analysis that combined child mortality with infant mortality. This post hoc analysis was justified on the basis that infant mortality accounts for 70% of under‐five mortality (Analysis 1.2). Overall, under‐five mortality may be reduced by IMCI (RR 0.85, 95% CI 0.78 to 0.93; two trials; 65,570 participants).

Nutritional status

Three studies assessed nutritional status; we have summarized their findings in Table 4 (Arifeen 2009; Bhandari 2012; Schellenberg 2004). Published data from Arifeen 2009 were not cluster‐adjusted, so we used an ICC of 0.01 in the meta‐analysis (see Methods).

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Table 4. Results: nutritional parameters

Parameter

Study

Study design

Pre‐intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Wasting

Arifeen 2009a

Cluster RCT

21.5%

(74/346)

21.6%

(95/439)

12.6%

(89/706)

14.3%

(101/709)

Schellenberg 2004b

CBA

12.57%

(21/167)

10.5%

(21/200)

6.8%

(13/191)

5.6%

(10/177)

Bhandari 2012

Cluster RCT

16.6%

(243/1461)

14.3%

(202/1412)

Stunting

Arifeen 2009c

Cluster RCT

63.1%

(334/530)

62.5%

(432/692)

50.4%

(599/1189)

57.1%

(674/1180)

Schellenberg 2004c,d

CBA

59.7%

(297/497)

51.1%

(247/483)

42.6%

(249/585)

40.0%

(191/477)

Bhandari 2012

Cluster RCT

49.6%

(725/1461)

48.2%

(680/1412)

Low weight for age

Schellenberg 2004e

CBA

30.6%

(290/947)

26.3%

(238/905)

23.4%

(234/1001)

19.5%

(161/825)

HAZ score

Mean (SD)

Arifeen 2009

Cluster RCT

‐2.35 (0.20)

‐2.39 (0.33)

‐2.01 (0.14)

‐2.17 (0.20)

WHZ score

Mean (SD)

Arifeen 2009

Cluster RCT

‐1.18 (0.20)

‐1.23 (0.19)

‐0.77 (0.25)

‐0.84 (0.14)

CBA: controlled before‐after; HAZ: height for age z‐score; IMCI: integrated management of childhood illness; RCT: randomised controlled trial; WHZ: weight for age z‐score
aWHZ ≤ 2 in children 0 to 23 months of age. Data from baseline and end surveys

bWHZ ≤ 2 in children 12 to 23 months of age. Data from baseline and end surveys

cHAZ ≤ 2 in children 24 to 59 months of age. Data from baseline and end surveys

dWhen expressed as mean haz scores, differential change between IMCI and comparison districts reached statistical significance (data not available/depicted)

eWAZ ≤ 2. Data from baseline and end surveys

For stunting, all confidence intervals overlap, and we considered it not unreasonable to pool study results for the trials. Overall, we noted that there may be little or no effect on stunting (RR 0.94, 95% CI 0.84 to 1.06; two trials; low‐certainty evidence; Analysis 1.3).

For wasting, we used the same estimate for the ICC. Analysis shows there is probably little or no effect of IMCI on wasting (RR 1.04, 95% CI 0.87 to 1.25; two trials; moderate‐certainty evidence; Analysis 1.4).

The Tanzania CBA study gave similar estimates for both parameters.

Quality of care

Arifeen 2009 conducted extensive assessments of quality of care in facilities, but Schellenberg 2004 measured fewer parameters (Table 5). Again, these data were collected by direct observation.

Open in table viewer
Table 5. Results: quality (facility level)

Outcome

Study

Pre‐intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Index of integrated assessment (0 to 100)

Arifeen 2009a

85.0%

(150/176)

11.0%

(15/132)

Correct management of all illness

Arifeen 2009a

64.6%

(111/172)

10.2%

(13/131)

Children with dehydration correctly treated

Arifeen 2009a

28.7%
(1/4)

0.0%

(0/2)

Schellenberg 2004b

20.0%

(1/5)

0.0%

(0/3)

Child with pneumonia correctly treated

Arifeen 2009a

80.8%

(46/ 57)

3.4%

(1/ 31)

Schellenberg 2004b

19.5%

(45/231)

10.1%

(19/188)

Child with anaemia correctly treated

Arifeen 2009a

0.0%

(3)

0.0%

(5)

Child needing referral was referred

Arifeen 2009a

35.7%

(2/6)

25.0 %

(1/4)

Children with fever treated with antimalarials

Schellenberg 2004b

39.4%

(147/373)

44.5%

(153/344)

27.4%

(108/394)

34.2%

(80/234)

IMCI: integrated management of childhood illness
aData from health facility surveys done in 2003 and 2005 and estimates weighted by total number of sick children seen in facilities on survey days.

Baseline data collected in 2003, 1 year after initiation of facility‐based IMCI. Indicators based on IMCI health facility survey guidelines

bData from household surveys conducted in 1999 and 2002

Prescribing at health facilities was measured in two studies. Performance in IMCI groups appeared considerably improved in the Bangladesh trial, and a small improvement in pneumonia correctly treated was found in Schellenberg 2004, although the base performance level was low. Schellenberg 2004 also measured administration of antimalarials for fever and found little or no difference following IMCI implementation (Table 5). As certainty of the evidence was very low, we do not know whether IMCI has a consistent effect on prescribing at health facilities.

Three studies measured prescribing by lay health care workers (Table 6). Investigators examined appropriate treatment under direct observation for three common illnesses: diarrhoea (and oral rehydration salts (ORS) use), pneumonia (antibiotic use), and fever (malaria treatment). As certainty of the evidence was very low, we do not know whether IMCI had a consistent effect on prescribing by lay health care workers.

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Table 6. Results: quality (prescribing by lay health care workers)

Outcome

Study

Study design

Pre‐Intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Children with diarrhoea treated with ORS

Arifeen 2009

Cluster RCT

48%

(60/125)

30%

(32/108)

Schellenberg 2004a

CBA

24.7%

(21/85)

10.4%

(10/96)

25.3%

(23/91)

19.0%

(15/79)

Change in % of children with diarrhoea treated with ORS

Mohan 2011b

CBA

1.6%

0.7%

Children with suspected pneumonia treated with antibiotics

Arifeen 2009

Cluster RCT

52%
(156/300)

48%
(167/348)

CBA: controlled before‐after study; IMCI: integrated management of childhood illness; ORS: oral rehydration salts; RCT: randomised controlled trial
aProportion of children ill in the last 2 weeks of the survey at baseline and at end of study period who were taken to an appropriate health care provider

bData collected from 2 rounds of district‐level health surveys in districts that implemented IMCI in 2005 and in control districts matched for IMR and proportion of scheduled castes and scheduled tribes. Weighted average of percentage change in coverage levels calculated for the 2 groups

Arifeen 2009 examined the appropriateness of referrals (percentage of children coming to a facility who required referral and were actually referred) and found little or no difference between IMCI and non‐IMCI clusters (Table 5).

Overall we found no consistent effect of the intervention on quality of care provided to beneficiaries.

Coverage of IMCI deliverables

Vaccine coverage

All four studies evaluated immunization coverage among children in the study populations (Arifeen 2009; Bhandari 2012; Mohan 2011; Schellenberg 2004). Among these, three studied coverage of the measles vaccine and found probably little or no effect on measles vaccine coverage (RR 0.92, 95% CI 0.80 to 1.05; two trials; Tanzania CBA showed a similar result; Analysis 1.5).

Two studies evaluated coverage of the third dose of diphtheria, pertussis, and tetanus vaccine ‐ one with very low coverage at follow‐up (15.6% in the control group, 21.2% in the IMCI group; Bhandari 2012) and one with much higher coverage at follow‐up (81.9% IMCI; 93% control; Schellenberg 2004; Analysis 1.6). The pattern was the same as for measles vaccine, with little or no evidence of improved coverage with IMCI.

Vitamin A coverage

Two studies reported vitamin A supplementation coverage. In the Bangladesh trial (Arifeen 2009), coverage was high in both intervention and control areas at baseline and at follow‐up. In the Tanzania study, vitamin A coverage was low at baseline in both groups and was high at follow‐up in both groups (Table 7). Analysis of end values shows that there was probably slightly better coverage in the control group of the Bangladesh trial (Analysis 1.7). Overall, there is probably little or no effect of IMCI on vitamin A coverage.

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Table 7. Results: coverage (vaccines)

Parameter

Study

Study design

Pre‐intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Measles vaccine coverage

Arifeen 2009a,b

Cluster RCT

36.9%

(124/335)

32.2%

(131/406)

52.7%

(219/416)

57.4%

(239/417)

Bhandari 2012

Cluster RCT

11.1%

(226/2045)

16.8%

(339/2017)

Schellenberg 2004c

CBA

88.3%

(159/180)

89.4%

(194/217)

88.2%

(180/204)

93.0%

(172/185)

Change in coverage of all vaccines

Mohan 2011d,e

CBA

3.8%

11.1%

DPT3 vaccine coverage

Bhandari 2012

Cluster RCT

15.6%

(318/2045)

21.2%

(427/2017)

Schellenberg 2004c

CBA

87.2%

(157/180)

85.3%

(185/217)

81.9%

(167/204)

95.1%

(176/185)

Vitamin A supplementation coverage

Arifeen 2009a

Cluster RCT

82.1%

(272/331)

74.4%

(301/405)

85.3%

(355/416)

91.7%

(381/415)

Schellenberg 2004c

CBA

12.9%

(25/194)

13.5%

(28/208)

77%

(154/200)

76.8%

(142/185)

CBA: controlled before‐after study; DPT: Diphtheria‐Pertussis‐Tetanus; IMCI: integrated management of childhood illness; RCT: randomised controlled trial

aData available from 6 monthly household surveys at baseline and at end

bData collected from vaccination cards

cData collected through information or registration during household surveys

dData collected from 2 rounds of district‐level health surveys in districts that implemented IMCI in 2005 and in control districts matched for IMR and proportion of scheduled castes and scheduled tribes. Weighted average of percentage change in coverage levels calculated for the 2 groups

eChange in proportion of children fully immunized

Appropriate care seeking

Care seeking was studied through various parameters in all four included studies with mixed results: Arifeen 2009 suggested improvement in the IMCI group, as did Bhandari 2012 (Table 8; Analysis 1.9). Schellenberg 2004 did not demonstrate improvement. Mohan 2011 reported on this and suggested better care seeking for ARI.

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Table 8. Results: coverage (care seeking behavior)

Outcome

Study

Study design

Pre‐intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Change (%) children with ARI seeking care

Mohan 2011a

CBA

NA

NA

+6.7%

‐11.1%

Appropriate care seeking

Bhandari 2012b

Cluster RCT

NA

NA

46.9%

(474/1010)

29.5%

(374/1269)

Arifeen 2009c

Cluster RCT

6%

(18/302)

4%

14/360)

24%

(111/462)

5%

(24/483)

Schellenberg 2004d

CBA

41.2%

211/512)

42.2%

(212/502)

38.2%

(203/531)

32.3%

(138/427)

Care seeking for children with danger signs

Schellenberg 2004d

CBA

53.1%

(86/162)

68%

(100/147)

54.9%

(78/142)

43.4%

(49/113)

ARI: acute respiratory infection; CBA: controlled before‐after study; IMCI: integrated management of childhood illness; IMR: infant mortality rate; RCT: randomised controlled trial
aData collected from 2 rounds of district‐level health surveys in districts that implemented IMCI in 2005 and in control districts matched for IMR and proportion of scheduled castes and scheduled tribes. Weighted average of percentage change in coverage levels calculated for the 2 groups

bProportion of neonates with danger signs who were taken to an appropriate health care provider (physician in government or private health facility or community health care worker)

cProportion of children ill in the last 2 weeks of the survey at baseline and at end of study period who were taken to an appropriate health care provider

dData from household surveys conducted in 1999 and 2002

Mohan 2011 also reported end values for "change in percentage of institutional deliveries," with 9.2% for IMCI and 5.0% for control and no differences in change detected (RR 4.2%, 95% CI ‐3.8 to 12.2).

Exclusive breast feeding

Exclusive breast feeding was reported in four studies (Table 9), which showed mixed results of very low certainty (Analysis 1.8): One study (Bhandari 2012), which included home visits to encourage breast feeding, found a large effect. Other measures related to breast feeding in this study followed this pattern; in the intervention group, fewer pre‐lacteal feeds were given and breast feeding was commenced within an hour of birth more commonly, although these measures were self reported. We noted little difference in relation to complementary feeding. The other three studies demonstrated no differences in breast feeding‐related parameters.

Open in table viewer
Table 9. Results: coverage (breast feeding and other child rearing practices)

Practice

Study

Study design

Pre‐intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Exclusive breast feeding

Bhandari 2012a,b

Cluster RCT

77.6%

(4811/6204)

37.3%

(2300/6163)

Arifeen 2009c

Cluster RCT

56.3%

(825/1466)

56.2%

(1021/1817)

75.5%

(1024/1356)

65.3%

(1149/1759)

Schellenberg 2004d

CBA

20.7%

(23/111)

26.1%

(18/69)

22.7%

(15/66)

32.1%

(17/53)

Mohan 2011e

CBA

30.0%

24.3%

Complementary feeding

Arifeen 2009f

Cluster RCT

60.4%

(734/1216)

52.8%

(873/1653)

67.6%

(792/1172)

57.2%

(783/1369)

Schellenberg 2004f

CBA

89.9%

(71/79)

95.9%

(70/73)

98.8%

(80/81)

98.7%

(74/75)

Bhandari 2012g

Cluster RCT

33.6%

(687/2045)

37.6%

(759/2017)

Pre‐lacteal feeds not given

Bhandari 2012a

Cluster RCT

80.2%

(4977/6204)

32.6%

(2006/6163)

Breast feeding initiated

within 1 hour of birth

Bhandari 2012a

Cluster RCT

40.7%

(2527/6204)

11.2%

(689/6163)

Mohan 2011e

CBA

18.1%

13.6%

Newborn care practices

Delayed bathing

Bhandari 2012a

Cluster RCT

84.5%

(5243/6204)

46.2%

(2848/6163)

Cord care

Bhandari 2012a,h

Cluster RCT

84.1%

(5219/6204)

39.5%

(2436/6163)

Appropriate clothing

Skin‐to‐skin contact on day of birth

Bhandari 2012a

Cluster RCT

97.5%

(6048/6204)

1.7%

(108/6204)

97.9%

(6036/6163)

0.0%

(2/6163)

CBA: controlled before‐after study; IMCI: integrated management of childhood illness; RCT: randomised controlled trial
aA separate team of research assistants interviewed a randomly selected subset of mothers at 29 days to ascertain newborn care practices

bExclusive breast feeding at 4 weeks of life

cChildren < 6 months exclusively breast feeding. Data from baseline and end population surveys

dChildren younger than 4 months exclusively breast fed

eData collected from 2 rounds of district‐level health surveys in districts that implemented IMCI in 2005 and in control districts matched for IMR and proportion of scheduled castes and scheduled tribes. Weighted average of percentage change in coverage levels calculated for the 2 groups

fChildren aged 6 to 9 months receiving both breast feeding and complementary food. Data from baseline and end population surveys

gInfants who received solid, semi solid, or soft foods in previous 24 hours and started complementary feeding between 6 and 8 months of age

hNothing or Gentian Violet applied to the cord

Newborn care practices

Bhandari 2012 examined several newborn care practices following implementation of IMCI. These practices included delayed bathing, cord care, and appropriate temperature maintenance. Investigators found improvement in all practices, except use of appropriate clothing to maintain newborn temperature while preventing hypothermia.

Discussion

Summary of main results

See summary of findings Table for the main comparison.

The integrated management of childhood illness (IMCI) strategies evaluated in these four studies included training of health care staff and management strengthening of health systems (all four studies), as well as home visiting (two studies). Two studies from India included care packages targeting the neonatal period.

Two studies (Tanzania and Bangladesh) showed that child mortality may be lower with IMCI, possibly as much as 28‐32% lower, but the confidence interval also included no effect.

One study in India, which implemented the integrated management of neonatal and childhood illness (IMNCI) strategy, including post‐natal home visits, examined infant and neonatal mortality, suggesting that neonatal and infant mortality may be lower in the IMNCI group than in the control group.

Three studies (Tanzania, India, Bangladesh) evaluated nutritional status and noted little or no effect on both stunting and wasting.

Investigators measured quality of care by observing prescribing for common illnesses in two studies (Tanzania and Bangladesh). Effects were mixed and ranged from no effect to quite large effects, so we do not know whether the effect on prescribing quality was consistent.

For coverage of IMCI deliverables, we examined vaccine coverage, appropriate care seeking, and exclusive breast feeding. Three studies (Tanzania, India, Bangladesh) estimated vaccine coverage for measles, reporting probably little or no effect on measles vaccine coverage; two of these studies measured the third dose of diphtheria, pertussis, and tetanus vaccine; and two measured vitamin A coverage, all providing little or no evidence of increased coverage with IMCI.

Four studies (two from India and one each from Tanzania and Bangladesh) reported appropriate care seeking, using information derived from careful questioning of mothers about recent illness. IMCI areas may show better reported care seeking behavior in some studies, but not in others.

All four studies recorded maternal responses on exclusive breast feeding. Results were mixed and were of very low certainty, with some studies indicating that exclusive breast feeding was higher in IMCI areas but was not very different in others.

No study reported satisfaction of mothers and service users.

Overall completeness and applicability of evidence

All included studies involved study populations from low‐ to middle‐income countries (LMICs) with high infant and child mortality rates; these settings are expected to benefit from IMCI interventions. Three of the four studies evaluated the impact of all three components of IMCI, and the fourth did not include the community component. Thus all four studies did include the two important components, namely, training of workers and strengthening of health care systems, but most also included the community component. The nature of interventions under each heading varied among trials (see Table 1).

All included studies were substantive in scope and in length of follow‐up. Control groups in all trials were comparable with intervention groups at baseline and continued to receive routine health care services as per ongoing programs. Thus any observed effects in the intervention groups are more likely to be attributable to the IMCI strategy than to spontaneous improvements noted over time. Evidence from these trials is largely applicable to real‐life situations among populations in LMICs.

Three (out of four) studies were conducted in South Asia ‐ two of these in India; thus the evidence base from African settings is particularly sparse.

Control groups in all studies received health care, so these studies evaluated the added value of IMCI or IMNCI. Such added value is likely to show a modest effect.

Quality of the evidence

Integrated management of childhood illness is a complex intervention, and conducting field trials to assess its impact is undoubtedly a challenging task. Therefore, generated evidence is valuable even if it is graded by the GRADE (Grades of Recommendation, Assessment, Development and Evaluation Working Group) approach as having low to moderate certainty (summary of findings Table for the main comparison). Of the four studies included in this review, two were carefully conducted cluster‐randomised controlled trials (Arifeen 2009; Bhandari 2012) with low risk of selection and recruitment bias, no attrition (loss of clusters), and good baseline comparability. The two controlled before‐after studies (Mohan 2011; Schellenberg 2004) were cluster studies with purposive selection of control and intervention clusters.

All studies included in this systematic review had been funded or supported by the World Health Organization (WHO) or had serving employees of WHO as co‐authors. As the World Health Organization is the primary institution responsible for facilitating global advocacy and implementation of IMCI, we were concerned about competing interests resulting in over‐optimistic interpretation of study results. However, included studies were generally well conducted and reported.

Potential biases in the review process

Two of the studies were conducted in India, and the lead and senior authors are familiar with these research studies in their own country. However, the authorship team was aware of this potential bias and ensured that application of inclusion criteria, data extraction, and interpretation were neutral. During the process of peer review, we became aware of another trial (Boone 2016) that might be eligible for inclusion in the review and will be included when we update this review. It is unlikely that we missed any trials because such trials are likely to be large, to require extensive funding, and to be of interest to the World Health Organization, which promotes this strategy. Therefore they are likely to have been picked up by our exhaustive search strategy, which included contacting all relevant stakeholders to identify eligible trials.

Agreements and disagreements with other studies or reviews

To our knowledge, no published systematic review has assessed the impact of IMCI implementation in population settings (in children younger than five) on mortality and other outcomes.

A recently published systematic review (Willey 2013) assessed the effectiveness of interventions to strengthen national health service delivery; the findings are consistent with our review.

Another systematic review (Nguyen 2013) assessed the impact of IMCI on the skills of health care workers. This review included cluster‐randomised controlled trials (RCTs), pre/post studies, and cross‐sectional studies and found that IMCI‐trained workers performed better in classifying illnesses, prescribing medications, vaccinating children, counselling families, and administering oral therapies. We did not consider these outcomes in our review.

We identified two trials (Amorim 2008; Rowe 2011) that were excluded because they were non‐randomised controlled trials with single comparison units. Notes of these findings are appended in the Characteristics of excluded studies table).

Study flow diagram.
Figuras y tablas -
Figure 1

Study flow diagram.

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
Figuras y tablas -
Figure 2

Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
Figuras y tablas -
Figure 3

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Comparison 1 IMCI versus standard services, Outcome 1 Mortality.
Figuras y tablas -
Analysis 1.1

Comparison 1 IMCI versus standard services, Outcome 1 Mortality.

Comparison 1 IMCI versus standard services, Outcome 2 Mortality (infant and child combined).
Figuras y tablas -
Analysis 1.2

Comparison 1 IMCI versus standard services, Outcome 2 Mortality (infant and child combined).

Comparison 1 IMCI versus standard services, Outcome 3 Stunting.
Figuras y tablas -
Analysis 1.3

Comparison 1 IMCI versus standard services, Outcome 3 Stunting.

Comparison 1 IMCI versus standard services, Outcome 4 Wasting.
Figuras y tablas -
Analysis 1.4

Comparison 1 IMCI versus standard services, Outcome 4 Wasting.

Comparison 1 IMCI versus standard services, Outcome 5 Measles vaccine coverage.
Figuras y tablas -
Analysis 1.5

Comparison 1 IMCI versus standard services, Outcome 5 Measles vaccine coverage.

Comparison 1 IMCI versus standard services, Outcome 6 DPT vaccine coverage.
Figuras y tablas -
Analysis 1.6

Comparison 1 IMCI versus standard services, Outcome 6 DPT vaccine coverage.

Comparison 1 IMCI versus standard services, Outcome 7 Vitamin A vaccine coverage.
Figuras y tablas -
Analysis 1.7

Comparison 1 IMCI versus standard services, Outcome 7 Vitamin A vaccine coverage.

Comparison 1 IMCI versus standard services, Outcome 8 IMCI deliverable ‐ exclusive breast feeding.
Figuras y tablas -
Analysis 1.8

Comparison 1 IMCI versus standard services, Outcome 8 IMCI deliverable ‐ exclusive breast feeding.

Comparison 1 IMCI versus standard services, Outcome 9 Appropriate care seeking.
Figuras y tablas -
Analysis 1.9

Comparison 1 IMCI versus standard services, Outcome 9 Appropriate care seeking.

Summary of findings for the main comparison. Integrated management of childhood illness strategy compared with routine care

Patient or population: children < 5 years of age

Settings: middle‐ and low‐income countries

Intervention: integrated management of childhood illness

Comparison: usual health services

Outcomes

Illustrative comparative risks* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Certainty of the evidence
(GRADE)

Comments

Assumed risk

Corresponding risk

Control

IMCI

Mortality

Child mortality

Risk ratio 0.87a

(0.68 to 1.10)

5090 children

(1 trial)1

⊕⊕⊝⊝

Lowb,c

due to indirectness and imprecision

Child mortality may be decreased, but confidence intervals include no effect

31 per 1000 live births

27 per 1000 live births
(21 to 34)

Infant mortality

HR 0.85

(0.77 to 0.94)

60,480e

(1 trial) 2

⊕⊕⊝⊝
Lowf,g,h

due to indirectness and imprecision

Infant mortality may decrease

69 per 1000 live births

59 per 1000 live births

(54 to 65)d

Nutritional status

Stunting

Risk ratio 0.94i

(0.84 to 1.06)

5242

(2 trials) 1,2

⊕⊕⊝⊝
Lowb,f,j

due to indirectness and imprecision

Little or no effect on stunting possible

57 per 100

53 per 100

(48 to 60)

Wasting

Risk ratio 1.04i

(0.87 to 1.25)

4288

(2 trials) 1,2

⊕⊕⊕⊝
Moderateb,j

due to indirectness

Probably little or no effect on wasting

13 per 100

14 per 100

(11 to 16)

Quality of care

Prescribing at health facilities

Mixed effectsk

727

(2 studies)1,3

⊕⊝⊝⊝

Very lowl,m

due to imprecision, inconsistency, and indirectness

Not known whether consistent effect on prescribing quality at health facilities

Prescribing by lay health care workers

No consistent effects

1051 observations

(3 studies)1,3,4

⊕⊝⊝⊝

Very lowl,m

due to imprecision, inconsistency, and indirectness

Not known whether consistent effect on prescribing quality of lay health care workers

Coverage of IMCI deliverables

Vaccine coverage (measles)

RR 0.92

(0.80 to 1.05)

4895

(2 trials) 1,2

⊕⊕⊕⊝

Moderaten,j

due to indirectness

Probably little or no effect on measles vaccine coveragen

57/100

54/100

(46 to 60)

Supplement coverage (vit A)

RR 0.93

(0.88 to 0.98)

831

(1 trial)1

⊕⊕⊕⊝

moderaten,j

due to indirectness

Probably little or no effect on vitamin A coverage

83 per 100

77 per 100

(73 to 81)

Appropriate care seeking

Mixed effectso

4182

(3 studies)1,2,3

⊕⊕⊝⊝
Lowp

due to inconsistency

Appropriate care seeking possibly improved in some studies, but not in others

Exclusive breast feeding

Mixed effectsq

7975

(4 studies) 1,2,3,4

⊕⊝⊝⊝
Very lowp,r,s,t,u

due to indirectness and inconsistency

Not known whether effect on exclusive breast feeding

Satisfaction of beneficiaries

Not measured

Not known whether users prefer IMCI or usual clinics

The basis for assumed risk is median control group risk across studies. The corresponding risk (and its 95% confidence interval) is based on assumed risk in the comparison group and relative effect of the intervention (and its 95% CI)
CI: confidence interval; ICC: intracluster correlation co‐efficient; RR: risk ratio

GRADE Working Group grades of evidence
High certainty: We are very confident that the true effect lies close to the estimate of effect
Moderate certainty: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of effect but may be substantially different
Low certainty: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of effect
Very low certainty: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect.

aIn the Bangladesh trial, mortality declined over the 5 years from 43 per 1000 live births to 27 per 1000 live births in the intervention area (reduced by 37%), and from 44.8 per 1000 live births to 31.2 per 1000 live births in control areas (reduced by 30%). A small difference in the reduction in child mortality was noted in the 2 groups (8.6% in the intervention group vs 7.8% in control groups).

The Tanzanzia CBA study had mortality estimates that were very similar to the Bangladesh trial (RR 0.87, 95%CI 0.72 to 1.05).

bDowngraded by 1 for serious indirectness: The Bangladesh trial modified the intervention after early analysis for care seeking and referral completion, suggesting that coverage was not increasing as expected. This included modification of treatment and referral guidelines and introduction of a new cadre of village health care workers trained and equipped to provide community case management for pneumonia and diarrhoea in 2005. These adjustments, including the new staff cadre, were in response to an intermediate process evaluation in the trial, and are unlikely to be mirrored in routine implementation programmes.

cDowngraded by 1 for imprecision: 95% CI is wide and includes a clinically important reduction in mortality and no effect. In addition, dominant change was secular (see note 1)

dAbsolute rates were calculated from hazard ratio by using the formula RR = (1 ‐ exp(HR ×ln(1 ‐ assumed risk)))/assumed risk

eIMCI in this trial included perinatal and neonatal components

fDowngraded for serious imprecision. Confidence intervals include no important effect to an important effect

gDowngraded by 1 for serious indirectness: This single study was conducted in a mixed rural/urban population in northern India with a substantive neonatal component with home visiting. Findings may not be easily generalized to other settings in Asia or elsewhere

hSubgroup analysis showed lower mortality in the intervention group among babies delivered at home, with no effect apparent in the subgroup delivering at hospital. This subgroup effect was evident for both neonatal and infant mortality

iConfidence intervals for Arifeen adjusted assuming ICC of 0.01

j The Tanzania CBA study has very similar estimates compatible with this estimate

kLarge improvements in 6 parameters in Arifeen; no clear effect in 2 parameters in Schellenberg

lDowngraded by 1 for both imprecision and inconsistency. Small numbers of participants observed; effect varies between trials and parameters measured

mDowngraded by 1 for indirectness. All measurements through direct observation of health care worker; may not represent behavior unobserved

nDowngraded by 1 for indirectness. Approximately 80% of the estimate taken from 1 study, so generalisability to other settings is uncertain

oPoint estimate for vaccine coverage suggests higher coverage in control group, and 95% confidence intervals exclude beneficial effect of IMCI on coverage.

pThis outcome was measured in various ways by different studies on samples of patients. Large improvements noted in some studies but not in others. As the outcome was so varied, we did not prepare a meta‐analysis

qDowngraded by 2 for inconsistency. Some large effects in some studies, and modest/no effects in others

rMixed effects between the 4 studies preclude meta‐analysis

sDowngraded by 2 for inconsistency. Large amounts of qualitative heterogeneity

tDowngraded by 1 for indirectness. See (b) above and the large effects seen in Bhandari associated with several home visits, which would not be feasible in other settings

uDowngraded by 1 for risk of bias. Breast feeding was reported through questionnaire from health care workers to mothers

Studies

1 Arifeen 2009;2 Bhandari 2012; 3 Schellenberg 2004 ; 4 Mohan 2011

Figuras y tablas -
Summary of findings for the main comparison. Integrated management of childhood illness strategy compared with routine care
Table 1. IMCI components

Schellenberg 2004

Arifeen 2009

Mohan 2011

Bhandari 2012

Human resources policies for health care professionals

IMCI training

Basic health care worker

Y

Y

Y

Y

Senior/other

Y

Y

Doctors

Y

TBA

Y

Refresher

Private sector

Y

Staff recruitment

Filling vacancies

Y

New cadre of community health care worker (CHW)

Y

Conditions of service

Cash incentives

Y

Management

Home visits

Y

Y

Y

Supervision and monitoring

Y

Y

Y

Health system strengthening

Tools and manuals including guidelines

Supply education materials

Y

Y

Additional equipment and drugs

Drug supply

Ya

Y

Y

Y

Supply minor equipment

Y

Strategies for community engagement

Training

Unqualified village doctors

Y

Y

Social development

Establishing mother/women group meetings

Y

Y

Support of community leaders/volunteers

Y

Community theatre

Y

IMCI: integrated management of childhood illness; TBA: traditional birth attendant

aAssumed, as the study is an assessment of first 2 components of World Health Organization (WHO) generic integrated management of childhood illness (IMCI)

Figuras y tablas -
Table 1. IMCI components
Table 2. Details of inputs described narratively

Study

Input

Schellenberg 2004

Incorporated 2 components of integrated management of childhood illness (IMCI), namely, training of health care workers and health system strengthening. All health care workers at the primary level received 11 days of training. IMCI nutrition education and counselling cards for educating mothers were prepared after operational research and subsequently translated into Swahili language to improve community practices. Health systems were strengthened using IMCI processes and by providing financial resources of approximately $0.92 per capita to implementing districts

Arifeen 2009

Incorporated all 3 components of IMCI. Health care workers were trained using the 11‐day course, followed by a 3‐day course on breast feeding counselling. Health systems strengthening consisted of making additional drugs available in the intervention area, and setting up a facility‐level drug tracking and reporting system. Job aids such as weighing scales, timer to count respiratory rate, thermometers, chart booklets, and locally adapted cards as aids for counselling mothers were provided to all intervention clusters. To improve community practices, special emphasis was given to messages related to pneumonia and malnutrition and to 3 practice areas, namely, care seeking for sick children, home management of illness, and responsive feeding

Mohan 2011

Retrospectively collected data about IMCI implementation from 12 districts that started implementation in 2005. Details of the intervention have not been described specifically for these 12 districts but are available for the entire country as part of a standard guideline. Training consisted of the 8‐day course for community‐based workers and auxiliary nurse midwives and an additional 2 days for supervisors. Workers are supposed to receive basic drugs and supplies as per guidelines of the Reproductive and Child Health II and Integrated Child Development Scheme (ICDS) programs. Community health practices include home visits to all newborns during which health care workers ensure exclusive breast feeding, provide counsel on temperature maintenance, explain danger signs, assess newborns (and other sick children) and refer them to an appropriate health facility, if required

Bhandari 2012

Health care workers were trained with the 8‐day IMNCI Basic Health Worker Course, and specialists received the 11‐day IMNCI Course for Physicians. Health systems interventions included (1) strengthened supervision of community health care workers and nurses and filling of vacant supervisor positions; (2) task‐based incentives to include IMNCI activities; and (3) establishment of drug depots in villages to ensure regular supply of drugs. Community health care workers made scheduled post‐natal home visits, promoted breast feeding, delayed bathing, provided cord care, and responded to care seeking for illness. They also ran women's health group meetings to increase awareness of healthy newborn care practices

Figuras y tablas -
Table 2. Details of inputs described narratively
Table 3. Results: mortality

Outcome

Trial ID

Study design

Pre‐intervention mortality rate

Post‐intervention mortality rate

Cluster‐adjusted relative effect
(95% CI)

Coverage indicators

analysis summary

IMCI

Control

IMCI

Control

Neonatal mortality

Bhandari 2012a

Cluster RCT

32.6/1000 live births

(n NA)

32.4/1000 live births

(n NA)

41.9/1000 live births

(1244/29,667)

43/1000 live births

(1326/30,813)

Hazard ratio 0.91b,c

(0.80 to 1.03)

Adjusted for confounders

Infant mortality

Bhandari 2012

Cluster RCT

44.9/1000 live births

(n NA)

43.9/1000 live births

(n NA)

65 per 1000 live births

(1925/29,667)

69 per 1000 live births

(2136/30,813)

Hazard ratio 0.85b
(0.77 to 0.94)

Adjusted for confounders

Child mortality

Arifeen 2009d

Cluster RCT

43.0 per 1000 live births

(144/3348)

44.8 per 1000 live births
(179/3996)

27.0 per 1000 live births

(157/5815)

31.2 per 1000 live births

(221/7083)

Risk ratio 0.87

(0.66 to 1.14)

No effect after exclusion of injuriese

Schellenberg 2004f

CBA

27.2 per 1000 child‐years

(639/23,515)

27.0 per 1000 child‐years

(242/8977)

24.4 per 1000 child‐years

(1220/49,964)

28.2 per 1000 years

(619/21,965)

Risk ratio 0.87

(0.72 to 1.05)

No effect after adjustment

CBA: controlled before‐after study; IMCI: integrated management of childhood illness; RCT: randomised controlled trial
aBhandari 2012: Fieldworkers not involved with IMNCI implementation visited households monthly to identify new pregnancies. Infants were visited at 1, 3, 6, 9, and 12 months to determine survival

bBhandari 2012: Hazard ratio was calculated after adjustment for cluster design and potential confounders between groups (markers of poverty, literacy, access to services)

cBhandari 2012: Although the overall effect was not statistically significant, a subgroup analysis found that a statistically significant reduction in neonatal mortality was significantly lower in the subgroup born at home (adjusted HR 0.80, 95% CI 0.68 to 0.93)

dArifeen conducted a household census in 2000 and 2007 where the complete birth history of all ever married women between the age of 15 and 49 years was used to estimate yearly and 2 year mortality rates. The data pertains to mortality between day 7 and 5 years of life.

eAfter exclusion of deaths due to malformation and injury (causes not related to IMCI), no effect of IMCI was noted on mortality (data not available)

fThis is the value adjusted for baseline differences in mortality. Unadjusted value is 4.2/1000 fewer deaths (95% CI ‐4.1 to 12.4). Mortality was slightly higher in the control group at baseline. Schellenberg study (Schellenberg 2004)

Also estimated mortality difference after “ignoring the between district variation” as 13% lower mortality (95% CI 5% to 21% lower) (P value = 0.004); risk ratio 0.87 (95% CI 0.79 to 0.95)

Figuras y tablas -
Table 3. Results: mortality
Table 4. Results: nutritional parameters

Parameter

Study

Study design

Pre‐intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Wasting

Arifeen 2009a

Cluster RCT

21.5%

(74/346)

21.6%

(95/439)

12.6%

(89/706)

14.3%

(101/709)

Schellenberg 2004b

CBA

12.57%

(21/167)

10.5%

(21/200)

6.8%

(13/191)

5.6%

(10/177)

Bhandari 2012

Cluster RCT

16.6%

(243/1461)

14.3%

(202/1412)

Stunting

Arifeen 2009c

Cluster RCT

63.1%

(334/530)

62.5%

(432/692)

50.4%

(599/1189)

57.1%

(674/1180)

Schellenberg 2004c,d

CBA

59.7%

(297/497)

51.1%

(247/483)

42.6%

(249/585)

40.0%

(191/477)

Bhandari 2012

Cluster RCT

49.6%

(725/1461)

48.2%

(680/1412)

Low weight for age

Schellenberg 2004e

CBA

30.6%

(290/947)

26.3%

(238/905)

23.4%

(234/1001)

19.5%

(161/825)

HAZ score

Mean (SD)

Arifeen 2009

Cluster RCT

‐2.35 (0.20)

‐2.39 (0.33)

‐2.01 (0.14)

‐2.17 (0.20)

WHZ score

Mean (SD)

Arifeen 2009

Cluster RCT

‐1.18 (0.20)

‐1.23 (0.19)

‐0.77 (0.25)

‐0.84 (0.14)

CBA: controlled before‐after; HAZ: height for age z‐score; IMCI: integrated management of childhood illness; RCT: randomised controlled trial; WHZ: weight for age z‐score
aWHZ ≤ 2 in children 0 to 23 months of age. Data from baseline and end surveys

bWHZ ≤ 2 in children 12 to 23 months of age. Data from baseline and end surveys

cHAZ ≤ 2 in children 24 to 59 months of age. Data from baseline and end surveys

dWhen expressed as mean haz scores, differential change between IMCI and comparison districts reached statistical significance (data not available/depicted)

eWAZ ≤ 2. Data from baseline and end surveys

Figuras y tablas -
Table 4. Results: nutritional parameters
Table 5. Results: quality (facility level)

Outcome

Study

Pre‐intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Index of integrated assessment (0 to 100)

Arifeen 2009a

85.0%

(150/176)

11.0%

(15/132)

Correct management of all illness

Arifeen 2009a

64.6%

(111/172)

10.2%

(13/131)

Children with dehydration correctly treated

Arifeen 2009a

28.7%
(1/4)

0.0%

(0/2)

Schellenberg 2004b

20.0%

(1/5)

0.0%

(0/3)

Child with pneumonia correctly treated

Arifeen 2009a

80.8%

(46/ 57)

3.4%

(1/ 31)

Schellenberg 2004b

19.5%

(45/231)

10.1%

(19/188)

Child with anaemia correctly treated

Arifeen 2009a

0.0%

(3)

0.0%

(5)

Child needing referral was referred

Arifeen 2009a

35.7%

(2/6)

25.0 %

(1/4)

Children with fever treated with antimalarials

Schellenberg 2004b

39.4%

(147/373)

44.5%

(153/344)

27.4%

(108/394)

34.2%

(80/234)

IMCI: integrated management of childhood illness
aData from health facility surveys done in 2003 and 2005 and estimates weighted by total number of sick children seen in facilities on survey days.

Baseline data collected in 2003, 1 year after initiation of facility‐based IMCI. Indicators based on IMCI health facility survey guidelines

bData from household surveys conducted in 1999 and 2002

Figuras y tablas -
Table 5. Results: quality (facility level)
Table 6. Results: quality (prescribing by lay health care workers)

Outcome

Study

Study design

Pre‐Intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Children with diarrhoea treated with ORS

Arifeen 2009

Cluster RCT

48%

(60/125)

30%

(32/108)

Schellenberg 2004a

CBA

24.7%

(21/85)

10.4%

(10/96)

25.3%

(23/91)

19.0%

(15/79)

Change in % of children with diarrhoea treated with ORS

Mohan 2011b

CBA

1.6%

0.7%

Children with suspected pneumonia treated with antibiotics

Arifeen 2009

Cluster RCT

52%
(156/300)

48%
(167/348)

CBA: controlled before‐after study; IMCI: integrated management of childhood illness; ORS: oral rehydration salts; RCT: randomised controlled trial
aProportion of children ill in the last 2 weeks of the survey at baseline and at end of study period who were taken to an appropriate health care provider

bData collected from 2 rounds of district‐level health surveys in districts that implemented IMCI in 2005 and in control districts matched for IMR and proportion of scheduled castes and scheduled tribes. Weighted average of percentage change in coverage levels calculated for the 2 groups

Figuras y tablas -
Table 6. Results: quality (prescribing by lay health care workers)
Table 7. Results: coverage (vaccines)

Parameter

Study

Study design

Pre‐intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Measles vaccine coverage

Arifeen 2009a,b

Cluster RCT

36.9%

(124/335)

32.2%

(131/406)

52.7%

(219/416)

57.4%

(239/417)

Bhandari 2012

Cluster RCT

11.1%

(226/2045)

16.8%

(339/2017)

Schellenberg 2004c

CBA

88.3%

(159/180)

89.4%

(194/217)

88.2%

(180/204)

93.0%

(172/185)

Change in coverage of all vaccines

Mohan 2011d,e

CBA

3.8%

11.1%

DPT3 vaccine coverage

Bhandari 2012

Cluster RCT

15.6%

(318/2045)

21.2%

(427/2017)

Schellenberg 2004c

CBA

87.2%

(157/180)

85.3%

(185/217)

81.9%

(167/204)

95.1%

(176/185)

Vitamin A supplementation coverage

Arifeen 2009a

Cluster RCT

82.1%

(272/331)

74.4%

(301/405)

85.3%

(355/416)

91.7%

(381/415)

Schellenberg 2004c

CBA

12.9%

(25/194)

13.5%

(28/208)

77%

(154/200)

76.8%

(142/185)

CBA: controlled before‐after study; DPT: Diphtheria‐Pertussis‐Tetanus; IMCI: integrated management of childhood illness; RCT: randomised controlled trial

aData available from 6 monthly household surveys at baseline and at end

bData collected from vaccination cards

cData collected through information or registration during household surveys

dData collected from 2 rounds of district‐level health surveys in districts that implemented IMCI in 2005 and in control districts matched for IMR and proportion of scheduled castes and scheduled tribes. Weighted average of percentage change in coverage levels calculated for the 2 groups

eChange in proportion of children fully immunized

Figuras y tablas -
Table 7. Results: coverage (vaccines)
Table 8. Results: coverage (care seeking behavior)

Outcome

Study

Study design

Pre‐intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Change (%) children with ARI seeking care

Mohan 2011a

CBA

NA

NA

+6.7%

‐11.1%

Appropriate care seeking

Bhandari 2012b

Cluster RCT

NA

NA

46.9%

(474/1010)

29.5%

(374/1269)

Arifeen 2009c

Cluster RCT

6%

(18/302)

4%

14/360)

24%

(111/462)

5%

(24/483)

Schellenberg 2004d

CBA

41.2%

211/512)

42.2%

(212/502)

38.2%

(203/531)

32.3%

(138/427)

Care seeking for children with danger signs

Schellenberg 2004d

CBA

53.1%

(86/162)

68%

(100/147)

54.9%

(78/142)

43.4%

(49/113)

ARI: acute respiratory infection; CBA: controlled before‐after study; IMCI: integrated management of childhood illness; IMR: infant mortality rate; RCT: randomised controlled trial
aData collected from 2 rounds of district‐level health surveys in districts that implemented IMCI in 2005 and in control districts matched for IMR and proportion of scheduled castes and scheduled tribes. Weighted average of percentage change in coverage levels calculated for the 2 groups

bProportion of neonates with danger signs who were taken to an appropriate health care provider (physician in government or private health facility or community health care worker)

cProportion of children ill in the last 2 weeks of the survey at baseline and at end of study period who were taken to an appropriate health care provider

dData from household surveys conducted in 1999 and 2002

Figuras y tablas -
Table 8. Results: coverage (care seeking behavior)
Table 9. Results: coverage (breast feeding and other child rearing practices)

Practice

Study

Study design

Pre‐intervention

Post‐intervention

IMCI

% (n/N)

Control

% (n/N)

IMCI

% (n/N)

Control

% (n/N)

Exclusive breast feeding

Bhandari 2012a,b

Cluster RCT

77.6%

(4811/6204)

37.3%

(2300/6163)

Arifeen 2009c

Cluster RCT

56.3%

(825/1466)

56.2%

(1021/1817)

75.5%

(1024/1356)

65.3%

(1149/1759)

Schellenberg 2004d

CBA

20.7%

(23/111)

26.1%

(18/69)

22.7%

(15/66)

32.1%

(17/53)

Mohan 2011e

CBA

30.0%

24.3%

Complementary feeding

Arifeen 2009f

Cluster RCT

60.4%

(734/1216)

52.8%

(873/1653)

67.6%

(792/1172)

57.2%

(783/1369)

Schellenberg 2004f

CBA

89.9%

(71/79)

95.9%

(70/73)

98.8%

(80/81)

98.7%

(74/75)

Bhandari 2012g

Cluster RCT

33.6%

(687/2045)

37.6%

(759/2017)

Pre‐lacteal feeds not given

Bhandari 2012a

Cluster RCT

80.2%

(4977/6204)

32.6%

(2006/6163)

Breast feeding initiated

within 1 hour of birth

Bhandari 2012a

Cluster RCT

40.7%

(2527/6204)

11.2%

(689/6163)

Mohan 2011e

CBA

18.1%

13.6%

Newborn care practices

Delayed bathing

Bhandari 2012a

Cluster RCT

84.5%

(5243/6204)

46.2%

(2848/6163)

Cord care

Bhandari 2012a,h

Cluster RCT

84.1%

(5219/6204)

39.5%

(2436/6163)

Appropriate clothing

Skin‐to‐skin contact on day of birth

Bhandari 2012a

Cluster RCT

97.5%

(6048/6204)

1.7%

(108/6204)

97.9%

(6036/6163)

0.0%

(2/6163)

CBA: controlled before‐after study; IMCI: integrated management of childhood illness; RCT: randomised controlled trial
aA separate team of research assistants interviewed a randomly selected subset of mothers at 29 days to ascertain newborn care practices

bExclusive breast feeding at 4 weeks of life

cChildren < 6 months exclusively breast feeding. Data from baseline and end population surveys

dChildren younger than 4 months exclusively breast fed

eData collected from 2 rounds of district‐level health surveys in districts that implemented IMCI in 2005 and in control districts matched for IMR and proportion of scheduled castes and scheduled tribes. Weighted average of percentage change in coverage levels calculated for the 2 groups

fChildren aged 6 to 9 months receiving both breast feeding and complementary food. Data from baseline and end population surveys

gInfants who received solid, semi solid, or soft foods in previous 24 hours and started complementary feeding between 6 and 8 months of age

hNothing or Gentian Violet applied to the cord

Figuras y tablas -
Table 9. Results: coverage (breast feeding and other child rearing practices)
Comparison 1. IMCI versus standard services

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Mortality Show forest plot

3

Rate Ratio (Fixed, 95% CI)

Totals not selected

1.1 Neonatal mortality (RCT)

1

Rate Ratio (Fixed, 95% CI)

0.0 [0.0, 0.0]

1.2 Infant mortality (RCT)

1

Rate Ratio (Fixed, 95% CI)

0.0 [0.0, 0.0]

1.3 Child mortality (RCT)

1

Rate Ratio (Fixed, 95% CI)

0.0 [0.0, 0.0]

1.4 Child mortality (CBA)

1

Rate Ratio (Fixed, 95% CI)

0.0 [0.0, 0.0]

2 Mortality (infant and child combined) Show forest plot

2

Rate Ratio (Fixed, 95% CI)

0.85 [0.78, 0.93]

2.1 Child mortality

1

Rate Ratio (Fixed, 95% CI)

0.87 [0.68, 1.10]

2.2 Infant mortality

1

Rate Ratio (Fixed, 95% CI)

0.85 [0.77, 0.94]

3 Stunting Show forest plot

3

Risk Ratio (Random, 95% CI)

Subtotals only

3.1 Cluster RCTs

2

Risk Ratio (Random, 95% CI)

0.94 [0.84, 1.06]

3.2 CBA studies

1

Risk Ratio (Random, 95% CI)

1.06 [0.92, 1.23]

4 Wasting Show forest plot

3

Risk Ratio (Fixed, 95% CI)

Subtotals only

4.1 Cluster RCTs

2

Risk Ratio (Fixed, 95% CI)

1.04 [0.87, 1.25]

4.2 CBA studies

1

Risk Ratio (Fixed, 95% CI)

1.20 [0.54, 2.68]

5 Measles vaccine coverage Show forest plot

3

Risk Ratio (Fixed, 95% CI)

Subtotals only

5.1 Cluster RCTs

2

Risk Ratio (Fixed, 95% CI)

0.92 [0.80, 1.05]

5.2 CBA studies

1

Risk Ratio (Fixed, 95% CI)

0.95 [0.89, 1.01]

6 DPT vaccine coverage Show forest plot

2

Risk Ratio (Fixed, 95% CI)

Subtotals only

6.1 Cluster RCTs

1

Risk Ratio (Fixed, 95% CI)

0.95 [0.68, 1.33]

6.2 CBA studies

1

Risk Ratio (Fixed, 95% CI)

0.86 [0.80, 0.92]

7 Vitamin A vaccine coverage Show forest plot

2

Risk Ratio (Fixed, 95% CI)

Subtotals only

7.1 Cluster RCTs

1

Risk Ratio (Fixed, 95% CI)

0.93 [0.88, 0.98]

7.2 CBA studies

1

Risk Ratio (Fixed, 95% CI)

1.00 [0.90, 1.12]

8 IMCI deliverable ‐ exclusive breast feeding Show forest plot

3

Risk Ratio (Fixed, 95% CI)

Totals not selected

8.1 Cluster RCTs

2

Risk Ratio (Fixed, 95% CI)

0.0 [0.0, 0.0]

8.2 CBA studies

1

Risk Ratio (Fixed, 95% CI)

0.0 [0.0, 0.0]

9 Appropriate care seeking Show forest plot

3

Risk Ratio (Fixed, 95% CI)

Totals not selected

Figuras y tablas -
Comparison 1. IMCI versus standard services