Development of paediatric quality of inpatient care indicators for low-income countries - A Delphi study
© Ntoburi et al; licensee BioMed Central Ltd. 2010
Received: 4 May 2010
Accepted: 14 December 2010
Published: 14 December 2010
Indicators of quality of care for children in hospitals in low-income countries have been proposed, but information on their perceived validity and acceptability is lacking.
Potential indicators representing structural and process aspects of care for six common conditions were selected from existing, largely qualitative WHO assessment tools and guidelines. We employed the Delphi technique, which combines expert opinion and existing scientific information, to assess their perceived validity and acceptability. Panels of experts, one representing an international panel and one a national (Kenyan) panel, were asked to rate the indicators over 3 rounds and 2 rounds respectively according to a variety of attributes.
Based on a pre-specified consensus criteria most of the indicators presented to the experts were accepted: 112/137(82%) and 94/133(71%) for the international and local panels respectively. For the other indicators there was no consensus; none were rejected. Most indicators were rated highly on link to outcomes, reliability, relevance, actionability and priority but rated more poorly on feasibility of data collection under routine conditions. There was moderate to substantial agreement between the two panels of experts.
This Delphi study provided evidence for the perceived usefulness of most of a set of measures of quality of hospital care for children proposed for use in low-income countries. However, both international and local experts expressed concerns that data for many process-based indicators may not currently be available. The feasibility of widespread quality assessment and responsiveness of indicators to intervention should be examined as part of continued efforts to improve approaches to informative hospital quality assessment.
Delivery of good quality health care has considerable potential to reduce childhood deaths in low-income countries where mortality is high [1, 2]. However, both anecdotal and empirical evidence suggest that the quality of care offered in many facilities, both primary and referral, is generally poor [3–8]. Valid and reliable performance measures (indicators) can be used to evaluate quality of care and help health workers to improve it . In some high income countries, quality of care measures are increasingly recognized as a priority to help foster improvement and promote accountability, and substantial investments have been made in their development [10–12]. In contrast, relatively little effort has been put into developing such measures for low-income countries .
Recently, the WHO revised an earlier tool for assessing the quality of care in first-referral health care facilities (rural or district level hospitals) in developing countries, based on multi-country experience and informed by discussions at a global WHO meeting in Bali in 2007 . The WHO tool is based on the classical quality of care framework involving structure, process and outcome . Amendments can be made to this tool by countries to suit their local needs. Uptake of the tool will probably depend on "buy in" and support from influential persons in each country. Using this tool, structure and processes of care are rated on a simple semi-qualitative scale (the latter based on a convenience sample of 5 cases) making it useful for rapid appraisal of hospitals. However, such scores are of limited value if the aim is to provide an objective comparison between hospitals within a region or within hospitals at different periods - particularly if different observers use the tool.
The debate about which quality measures are best continues . Proponents of process measures argue that they directly measure actions that are within the control of health workers . However, without appropriate drugs and equipment, health workers may be unable to offer the correct care, making structure a limiting factor in quality improvement . Outcome measures may be intuitively the most useful indicators of quality, but their opponents argue that they are subject to considerable confounding and may require large samples for sufficiently precise measurement.
To decide which measures to use, expert judgement, supported by evidence where available, is often used. Experts, however, differ in opinion and a family of consensus methods such as the nominal group technique (NGT), the Delphi technique, and the RAND/UCLA appropriateness method (a hybrid of the former two), are often used to facilitate communication and avoid the negative social influences associated with group processes . This article reports the results of a Delphi study that aimed to determine which measures of quality of admission care for children in first level referral hospitals in low-income countries were widely supported, using explicit methods. Performance measures can be used to assess quality at different levels - clinical, organisation or population. This study considered measures pertinent to the clinical level. Further, the study aimed to identify process measures which could give quantitative measures of performance and performance change. We had a particular focus on the African setting and also examined the likely acceptability of internationally suggested indicators to an influential Kenyan audience. Ethical approval was obtained from the KEMRI National Ethical Review Committee.
It is recommended that expert panels be multidisciplinary and inclusive of individuals from geographically diverse and culturally disparate areas [20, 21]. This heterogeneity is thought to bring a wealth of experience and knowledge, and enhance the richness of the discussion. In the current study, two panels of experts were set up. Panel one, the International Panel, consisted of participants predominantly drawn from the 2007 WHO conference on quality of care for children, and members of an informal WHO-linked Paediatric Quality-of-Care email discussion group. Many have published work on quality of care in low-income settings . Panel two, the national panel, consisted of faculty from the Paediatric Department of the University of Nairobi and senior policy-makers in the Kenyan Ministry of Health. The characteristics of the experts are presented in Additional file 1.
Establishing the scope
Six common childhood topics were chosen for indicator development: malaria, pneumonia, diarrhoea, meningitis, malnutrition, and problems of the sick newborn. These conditions account for over 80% of morbidity and mortality in hospitals in low-income countries in Africa , including Kenya . It has been shown that the care provided for these conditions often varies considerably and is of poor quality [3, 6, 8, 24–27]. However, there are affordable and effective treatments for these conditions, defined by international guidelines promoted by the WHO/UNICEF and, in Kenya, by the government [28, 29]. These provide a useful quality standard.
From the generic WHO Hospital assessment tool and the associated international , evidence-based guidelines , researchers (SN, ME) developed a list of potential indicators. The indicators were equally distributed between those based on structure and those based on process of care. The number of process indicators considered for each condition (e.g. pneumonia, malaria etc) was similar. Outcome measures were not considered for the reasons alluded to above.
Some indicators were composites combining several stage-specific individual indicators. Experts were asked to indicate whether they preferred the composites to the individual constituent indicators. Experts were also asked to indicate in how many areas of the hospital providing paediatric or newborn care a specific item (e.g. a drug or piece of equipment) ought to be present before the item was considered, in aggregate, available at a hospital level.
The limited evidence suggests that better results can be achieved if the participants are given reviews of the literature [30, 31]. We did not do this because summarising the evidence would have been an unrealistically large task given the range of topics considered. Moreover, experience suggests that in fact there is often very little high quality evidence for commonly accepted best practices . Instead the experts were provided with both a link to the WHO guidelines for hospital care  and to a web-based resource where evidence behind the WHO guidance is progressively being archived http://www.ichrc.org.
International/WHO expert panel process
The international panel completed three rounds of questionnaires. The first questionnaire was sent in May 2008. This was accompanied by a covering letter giving information about the Delphi process such as the anticipated time required to complete the first questionnaire, how to contact the researchers in case of queries and the deadline for completing the round. In this first round, indicators were rated on only four attributes: link to outcome, reliability, relevance and actionability. Explanations of the attributes were given to the experts and are shown in Figure 1. In addition, experts were asked to suggest new indicators.
In the second round all the experts were provided with their own responses for each indicator and attribute, and the corresponding panel median responses from the first iteration. They were also provided with a summary of the written comments made in the first round complied by one of the investigators (ME) acting as a moderator. Experts were asked to reflect on the feedback and re-rate each item in light of this information. In a few instances, indicator statements were reworded because they were noted by the experts to be ambiguous on the first round. Additional indicators were included following suggestions made in the first round. Two additional attributes were also introduced: i) priority for reporting the indicator to the Ministry of Health and, ii) feasibility of data collection (Figure 1). Opinions on feasibility were requested for process-based indicators only as feasibility of indicator assessment was not considered to be an issue with structural elements - their presence or absence can easily be ascertained. We hoped that these additional attributes, together with the comments from the moderator, would assist the experts to decide which indicators could (feasibility) and should (priority) be included in routine quality assessment. A third round for this panel was conducted similarly. Reminders were regularly sent to the experts (range, 1- 4 reminders) and the process was completed in September 2008.
National panel process
The local panel of experts completed two rounds of the questionnaire. The experts were invited to the researchers' organization (KEMRI) in June 2008 and the study explained in a Microsoft PowerPoint® presentation. Then the experts completed the questionnaire in private. The international panel Round 2 questionnaire served as the first round for the national panel. The aggregated scores and summary of results from the WHO panel were however not included. The second round was completed 2 weeks later at the same venue, with experts again filling in the questionnaire in private. The questionnaire provided in this round presented the expert's own score and the indicator specific median response of the local panel. Experts were asked to consider revising their previous views in light of this information and the criterion of priority to the Ministry of Health was emphasised. The local expert opinion was used to assess the degree to which recommendations made by an international panel are endorsed in our local setting.
Median scores and frequency of responses in each tertile Likert category (1-3, 4-6, and 7-9) were calculated. We defined an indicator as being accepted with agreement according to the following pre-specified criteria (consensus criterion 1) :-
An indicator was accepted with agreement if two thirds or more of the experts rated the indicator in the upper tertile (7-9) on link to outcomes and a score of 4 or more on reliability, relevance and actionability.
An indicator was rejected with agreement if two thirds or more of the experts rated the indicator in the lowest tertile (1-3) on link to outcomes.
An indicator was classified as uncertain/equivocal if they did not fall in either of the above groups.
A second post hoc definition of indicator acceptance and agreement, using the same thresholds as above (for consensus criterion 1), but with the further requirement of 'good' agreement about the link to outcomes, defined as an inter-quartile range on the link to outcomes attribute not exceeding two (consensus criterion 2). This latter definition captures the fact that consensus within a group is reflected in smaller variance (smaller IQR) of the responses.
An indicator was defined as a priority for reporting, feasible currently or feasible with improvement if its median score for these specific attribute was 7 or more (consensus criterion 3). A post hoc consensus criterion 4 was defined as criterion 3 plus an IQR of less than 2 for these attributes. Finally the process indicators were ranked by ordering them (highest to lowest) using scores achieved on attributes using the following sequence: feasibility with current data, feasibility with improvement of data collection methods and priority for reporting. An indicator was ranked highly if it had high median score on these attributes with a narrow IQR on these attributes. The structure indicators were ranked by priority only. The Wilcoxon signed-rank test was used to test differences in ranking between the two panels. Consensus on the number of places in a hospital where an item must be present to define availability in aggregate was based on a simple majority view (more than 50%) of the experts.
Three-way kappa was used to evaluate reliability of views for the three levels of agreement: accepted, equivocal and rejected. The responses according to consensus criterion 1 from each panel from the final round were treated as responses from two raters for these analyses. The confidence intervals for kappa were obtained using bootstrap methods with 5000 replications. These analyses were carried out in Stata® version 10.2 (StataCorp, Texas, USA) using the kapci command and with Stata's pre-recorded weight, w, in measuring the importance of disagreements . The kappa values represent the proportionate agreement adjusted for chance and range from 0 (no agreement beyond chance) to 1 (perfect agreement).
Forty percent of those invited to the international panel declined the offer, citing reasons including lack of time and insufficient experience of the topic. 10% and 24 % of the international experts returning round 1 did not complete rounds 2 and 3 respectively. 16/19 of the local experts invited to participate in the process accepted the offer and all but one completed the process.
Changes between rounds in acceptance of indicators (n = 132 indicators)
Acceptance of care indicators by domain*
Equipment & drugs (n = 52)
Organisation (n = 14)
General (n = 7)
Cough/pneumonia/asthma (n = 15)
Fever/malaria/meningitis (n = 14)
Diarrhoea & dehydration (n = 11)
Malnutrition (n = 11)
Neonatal care (n = 8)
Top five indicators by domain†
Structure: drugs and equipment
1. The availability of intravenous fluids with physiological sodium concentrations (one or more of: Normal saline, Hartmann's solution, or Ringer's Lactate).
2. The availability of Epinephrine (Adrenaline) for injection.
3. The availability of the locally recommended first line oral antimalarial in settings where there is malaria.
4. The availability of Gentamicin.
5. The availability of vaccines including Pentavalent vaccine or DTP or DTP-HepB, BCG polio and measles vaccine in the hospital.
Structure: organisation of care
1. The presence of a system to prioritize severely ill children and group them together for observation in the ward.
2. The presence of a triage system in the outpatients department.
3. The presence of an area in the outpatients section of the hospital that is dedicated to provision of routine and walk-in services for children under 5 years only.
4. Proportion of all admitted children with documentation providing evidence that they were reassessed at least daily (during working days) by a doctor or clinical officer.
5. The availability of up to date hospital records describing paediatric admissions with diagnosis, age, sex and outcomes.
General care for severely ill children:
1. The proportion of children described as unable to feed/drink or with AVPU < V who are prescribed an appropriate fluid or feed regimen.
2. The proportion of children who have documentation that they were clinically assessed (wasting or oedema of Kwashiokor) or assessed with MUAC or WHZ for severe malnutrition.
3. The proportion of admitted children with documentation of assessment for 'danger signs' - these include convulsions, cyanosis, grunting, acidotic breathing, weak pulse, capillary refill, consciouness level (AVPU score) (in)ability to drink, neck stiffness or bulging fontanelle.
4. The proportion of Diazepam prescriptions for convulsions that are of the correct dose (iv or rectal doses according to national guidelines).
5. The proportion of prescriptions for injection Phenobarbitone that are the correct dose.
1. The proportion of children with pneumonia prescribed antibiotics at correct doses (correct dose is defined as weight appropriate dose according to WHO or local guidelines with a ± 20% range of acceptability).
2. The proportion of children prescribed oxygen correctly (including route device and flow rate).
3. The proportion of children with severe or very severe asthma correctly prescribed a steroid (including route of administration dose and frequency).
4. The proportion of children with a diagnosis of pneumonia who are correctly classified as having pneumonia severe pneumonia or very severe pneumonia (The correctness of classification must be based on documentation of appropriate supporting signs).
5. The proportion of children requiring oxygen (i.e. children with cyanosis or other signs of very severe pneumonia/asthma including grunting/head nodding/inability to drink or breastfeed/AVPU < A) actually prescribed oxygen
1. The proportion of children with fever in a malaria endemic area who are investigated for malaria (with either a blood slide or rapid test).
2. The proportion of children with malaria prescribed treatment antimalarial that is appropriate to the clinician's classification of severity and local guidelines (correct drug choice dose and frequency)
3. The proportion of children with the presence or absence of fever recorded in their medical notes.
4. The proportion of children with a primary diagnosis of malaria in whom the diagnosis is supported by a positive blood slide/rapid test for malaria.
5. The proportion of children with a diagnosis of meningitis prescribed correct antibiotics (first line appropriate for context or second line if known to have failed prior treatment) in correct doses.
Diarrhoea and dehydration:
1. The proportion of children with dehydration prescribed treatment (including right fluid type volume and rate) that is appropriate to their classification (including shock/severe and some dehydration) and weight.
2. The proportion of children with bloody diarrhoea given correct antibiotic (as recommended by the national guidelines).
3. A composite indicator of the proportion of children assessed completely. This include skin turgor, sunken eyes level of consciousness, ability to drink/breastfeed or sit, capillary refill, peripheral skin temperature and temperature gradient, presence of weak (absent) peripheral pulses, presence of acidotic breathing, irritability, urine output, malnutrition
4. The proportion of diarrhoea cases prescribed Zinc (where this is national policy) at correct dose for age.
5. The proportion of children with diarrhoea who have documentation of whether or not there is blood in the stool.
1. The proportion of children in HIV endemic areas with a diagnosis of severe malnutrition who are tested for HIV as an inpatient.
2. The proportion of children with a diagnosis of severe malnutrition prescribed appropriate parenteral antibiotics.
3. The proportion of children with a diagnosis of severe malnutrition receiving Vitamin A on admission.
4. The proportion of children with a diagnosis of severe malnutrition and dehydration prescribed appropriate rehydration fluid (ReSoMal or other low Sodium fluid e.g. half strength Darrows with potassium supplementation).
5. The proportion of children with a diagnosis of severe malnutrition prescribed the correct feed in the recommended volume and frequency.
1. The proportion of sick neonates with a diagnosis of neonatal sepsis prescribed the appropriate antibiotics (including correct choice of drug correct dose for weight and age frequency and route of administration according to guideline).
2. The proportion of babies born in hospital to HIV+ mothers who receive PMTCT therapy in line with national policy.
3. The proportion of babies born in hospital whose mothers have their HIV status known before delivery.
4. The proportion of babies aged <14 days prescribed routine Vitamin K in countries where this is national policy.
5. The proportion of newborn babies who get eye prophylaxis (Tetracycline Eye Ointment).
Indicators considered a priority or feasible‡
Consensus criterion 3§
Feasible with improvements
Feasible with improvements
Although much more demanding of information, more than half of the international experts expressed a preference for 6 out of the 7 composite indicators presented to them. These composite indicators span multiple processes in managing one case. Local experts preferred 5/7 of these indicators (Additional file 3). However, only a few experts in both panels preferred the proposed composite indicator for children with pneumonia, perhaps thinking it too complex and thus lacking feasibility. Based on simple majority voting, the experts suggested that most of the drugs or equipment needed to be in 2 or more specific areas offering care to children or newborns within the hospital to be considered available at a hospital level (for details see Additional file 4).
For drug doses, 14/15 of international experts and 7/11 local experts who answered the question agreed that a correct dose should be within a range of ± 20% of the dose for weight in the WHO or local guidelines. Using Likert scales we investigated whether the ability of laboratory to perform the following laboratory services was linked to outcomes: blood glucose (bedside); haemoglobin (or full blood count); microscopy or rapid test for malaria (where endemic); HIV testing; blood grouping and cross-matching; and CSF microscopy. All were scored highly (median scores greater than 7) though again opinions varied more for the local panel. Both expert panels tended to rate ability to measure bilirubin lowest (Additional file 3).
Agreement between panels' acceptance of care indicators at final round
Equipment & drugs (n = 52)
Organisation (n = 14)
All structure indicators (n = 66)
General (n = 7)
Cough/pneumonia/asthma (n = 15)
Fever/malaria/meningitis (n = 14)
Diarrhoea & dehydration (n = 11)
Malnutrition (n = 11) **
Neonatal care (n = 8) **
All process indicators (n = 66)
All indicators (n = 132)
This study sought to assess the perceived value and validity of a set of indicators of quality of inpatient care proposed for children and newborns admitted to hospital in low-income countries. It used a transparent and inexpensive method that combines scientific evidence and expert opinion. Additionally, we intended to investigate how well recommendations typically issued by international organisations such as the WHO might be accepted by local experts, as such views might influence their local credibility. The Delphi technique proved useful in both respects. The lack of an obligation to meet face to face significantly improved the feasibility of the study as cost was not a constraint on either the size or composition of the international expert panel . Most of the indicators proposed were considered: reliable and relevant to low-income settings; within the capabilities of resource constrained health systems to improve; able to identify areas urgently in need of attention and; to be feasible targets of data collection.
However, one of our anticipated project outputs was identification of a parsimonious set of indicators (about 20-30) that we felt might realistically form the basis of routine and widespread reporting to ministries of health in low-income countries. In this respect it can be argued that the process failed, with support for a large number of indicators of quality of care, making implementation of routine, national quality assessment incorporating all of these potentially more difficult. The demonstrated support for a large number of indicators might be interpreted as an endorsement of the scope and content of the original WHO assessment tool and, by extension, a desire to ensure that any assessment tool for hospital inpatient care should span the resources, assessment tasks and management required to provide effective care for multiple, important diseases. Alternatively it may reflect in part the numerous indicators presented to the experts. Presenting a large initial set of indicators was meant to minimize the risk of missing potentially important issues and prevent a small number of investigators (SN, ME) imposing their priorities at the outset. Interestingly some of the national panel, when prompted to prioritise indicators for reporting to the ministry of health, were more likely than members of the international panel to 'downgrade' indicators (although only to an uncertain status) producing a potentially shorter list and resulting in less apparent consensus in their final round.
It is reassuring that there were high levels of agreement between the local and international panels. Worth noting is the high agreement achieved on the sets of indicators for care of sick neonates and malnourished children. This may have been influenced by increasing recent appreciation globally of the high case fatality rates in these groups. Within panels however, there was somewhat more divergence (larger variance) around structural elements of care perhaps reflecting different experts' experiences of resource environments or the poor scientific evidence available supporting their contribution to better outcomes.
Responses on the feasibility of data collection for assessment of an indicator under current conditions in low-income settings varied, suggesting many panellists were concerned that assessment of many important process indicators requiring data from routine review of medical charts may not be possible currently. There was however optimism that measures could be instituted to improve quality of data. This concern is echoed more generally internationally , supported by experience nationally [38, 39]. However, an unexpected finding was that indicators for neonatal care were accorded generally higher scores on feasibility. Our experience of working in district hospitals in Kenya  and from published data elsewhere  seem contrary to these views. It is possible, therefore, that the views expressed by the experts on feasibility are overoptimistic and unduly influenced by their desire to promote certain indicators. Before any indicators are widely adopted they should be tested for feasibility and ability to detect significant change in performance (sensitivity) . We are in the process of evaluating the feasibility of the accepted set of indicators using data from 8 Kenyan district hospitals. More generally, improving the quality of care within a health system will need improvements in information system.
As our goal was to develop a tool that might be routinely used to provide quantitative measures of quality at scale within the capacity of an existing health system, our focus was case record review. However, there are alternative methods of collecting data on the process of care such as direct observation or use of vignettes. Direct observation may influence care, and would be time consuming and costly if a sample size sufficient to produce a quantitative estimate is desired . Vignettes, perhaps best for assessing health worker knowledge, have been used but similarly require organised access to multiple health workers and so may be hard to implement at scale in African settings .
There are potential limitations in our study that warrant mention. First, the results reported here represent the opinions of only a few, non-randomly selected individuals. However, our international panel had members with wide and long clinical and quality improvement experience in low-income settings. The local panel consisted largely of experts drawn from an academic referral centre. However, the local experts are influential, frequently called upon by government to provide expert technical advice and are responsible for training of health workers. They thus represent an important constituency in brokering the acceptance or rejection of international recommendations at a country level.
Second, we did not grade or present the strength of evidence linking indicators to outcomes in the questionnaires. This was in part due to the scale and scope of the task with considerable implications on workload for both the researchers and expert panellists. Moreover, the indicators were derived from the practices or resource implications of existing WHO recommendations for hospital care . Third, our definition of consensus, though based on published studies, remains somewhat arbitrary [30, 43]. Altering the definition of consensus, for example by calculating mean scores across attributes for each indicator, did not result in significant change in those accepted by the predefined criteria (data not shown). The post hoc analysis (consensus criterion 2) may be useful if the intention is to reduce the list of indicators. Fourth, the process did not involve experts meeting face to face. While this reduced the cost, many may argue that an opportunity for experts to meet would have stimulated useful discussion on contentious issues . We did however encourage experts to make comments which we then summarised and fed back to the group through a moderator.
Methodologically, some valuable lessons were learnt. First, Delphi studies are time consuming with an average turnabout time between rounds of approximately 1.5 months for emailed questionnaires. Second, the method of delivering the instructions may have an effect on the results of the process. The local panel received instructions by word of mouth and were more likely to prioritise indicators in round 2 compared to the international experts who were given written instructions. Finally, there is scope for refining definitions of consensus by allowing the participants to decide on an appropriate definition instead of imposing one.
Measurement of the quality of care is a prerequisite for determining whether quality of care is improving. Although there remains significant challenges in defining such measures, this study represents the first attempt at a transparent, consensus based, international approach to identify indicators of quality hospital care for children and newborns suitable for use in low-income settings. For process based measures, feasibility of data collection remains a concern and should be further evaluated. This study, based on a transparent process, helps formally define widely acceptable, quantitative indicators and provides a platform for further debate and continuing indicator development that should include the review and updating of indicators as priorities and technologies change and interventions to improve quality of care are scaled up. Such reviews may be more likely if a relatively inexpensive process such as the one described here is used.
Paediatric Quality of Hospital Care Indicator Panel
Amos Odiit, Makerere, UGANDA; Anthony Enemil, Kumasi, GHANA; Carolyn MacLennan, Dili, TIMOR L'OESTE & Melbourne, AUSTRALIA; Cindy Stephen, KwaZulu-Natal, SOUTH AFRICA; Trevor Duke, PAPUA NEW GUINEA & Melbourne, AUSTRALIA; Elizabeth Molyneux, Blantyre, MALAWI; Elmarie Malek, SOUTH AFRICA; Giorgio Tamburlini, Trieste, ITALY; Hugh Reyburn, Moshi, TANZANIA; Lulu Muhe, ETHIOPIA & WHO, Geneva, SWITZERLAND; Mark Patrick, KwaZulu-Natal, SOUTH AFRICA; Martin Weber, WHO, Geneva, SWITZERLAND; Mike English, Nairobi, KENYA; Steve Allen, The GAMBIA & Swansea, UK; Steve Graham, MALAWI & Melbourne, AUSTRALIA; Susanne Carai, WHO, Geneva, SWITZERLAND; Tabish Hazir, Islamabad, PAKISTAN.
We would like to thank the local experts who provided their expertise: University of Nairobi, KENYA panellists included: Aggrey Wassuna, Agnes Langat, Ahmed Laving, Anjumanara Omar, Christine Gichuhi, Dalton Wamalwa, Elizabeth Obimbo, Florence Murila, Grace Irimu, Mbori Ngacha, Nyambura Kariuki, Rachel Musoke, Ruth Nduati and, Yuko Jowi. Government of Kenya: Anna Wamae, Santau Migiro. We also acknowledge the participation of the following experts in rounds 1 and 2 of the Delphi international panel: Kalifa Bojang, Basse, The GAMBIA; Michael vanHensbroek, MALAWI & Amsterdam, The NETHERLANDS; Rajiv Bahl, WHO, Geneva, SWITZERLAND; Tsiri Agbenyega, Kumasi, GHANA; Severin von Xylander, WHO, VIET NAM. We are also grateful to Jim Todd (LSHTM, CPS, London, UK) for help in analysis, interpretation of the results and the drafting of this manuscript. This manuscript is published with the permission of the Director of KEMRI
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