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Making Every Baby Count

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Sometimes information concerning the birth and death from different sources may be contradictory.<br />

Although it is not the task of any one individual to reconcile such discrepancies,<br />

it is important that they are highlighted at the stage of data collection and synthesis, with<br />

plans to rectify inconsistencies in register data and move towards better-quality inputs. Data<br />

quality should be ensured at the data entry level. South Africa’s PPIP electronic database has<br />

a number of built-in validity checks (41). Some are automatic on the data entry page, and<br />

other validity checks can be activated once the monthly data have been entered (e.g. critical<br />

fields must be filled in before the next field can be activated for data entry, and implausible<br />

entries – such as 60 weeks gestational age, or 20 kg birth weight – are not permitted by the<br />

software. This minimizes the potential for missing or incorrect data. Data verification should<br />

happen at the facility level before local data are relayed to any higher levels.<br />

Variations in trend data (Annex 7) – for example, increases or decreases in deliveries or<br />

care-seeking behaviours – may need to be examined further with information from the<br />

community to understand possible explanations for these changes (see Chapter 4). Innovation<br />

and technology such as software programs can help, particularly in the rapid<br />

analysis and presentation of results, but should not be the focus of the audit process or a<br />

barrier to uptake.<br />

Step 3: Analysing information<br />

It is helpful to have an analytic plan to guide the process, keeping in mind that the overall<br />

goal is to identify problems in the system that may contribute to stillbirths and neonatal<br />

deaths, especially those that could have been prevented or avoided. To accomplish this,<br />

data analysis should ideally include both qualitative and quantitative components. The<br />

quantitative analysis, based on data such as geographic location and maternal risk factors,<br />

will provide information on which groups of babies are at higher risk of death, and identify<br />

trends in mortality rates and medical causes of death. Qualitative analysis of information<br />

about contributing factors and barriers to care, among others, will provide additional<br />

insight into the problems that caused the deaths of individual babies as well as more generally<br />

providing information about groups of babies affected by similar contributing factors.<br />

For example, qualitative data can help to answer questions about individual cases such as:<br />

Did the baby die because no one realized how sick it was or because the health centre was<br />

too far away? Were the right medicines not administered or were they unavailable? Collection<br />

(by interview) and review of such qualitative data can be particularly helpful for getting<br />

more information when patient notes in a particular case are very limited, for example if<br />

cause of death is simply noted as “already dead” or “arrived too late”. The use of both<br />

types of data together will provide a more rounded view of what the problems are and help<br />

the review committee identify priorities for action.<br />

While death reviews should not primarily be a process to produce data, there are a number<br />

of informative quantitative analyses and outcomes that can be tallied by the review committee<br />

or designated staff and presented at scheduled mortality audit meetings, as well<br />

as posted publically within the ward or unit. The minimum set of perinatal indicators that<br />

could be presented in this way include (49):<br />

• the number of normal vaginal, assisted and caesarean deliveries;<br />

• the number of maternal deaths;<br />

MAKING EVERY BABY COUNT: AUDIT AND REVIEW OF STILLBIRTHS AND NEONATAL DEATHS<br />

35

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