| Literature DB >> 31692720 |
Chigozie Jesse Uneke1, Henry Chukwuemeka Uro-Chukwu1, Onyedikachi Echefu Chukwu1.
Abstract
Reliable data on the cause of child death is the cornerstone for evidence-informed health policy making towards improving child health outcomes. Unfortunately, accurate data on cause of death is essentially lacking in most countries of sub-Saharan Africa due to the widespread absence of functional Civil Registration and Vital Statistics (CRVS) systems. To address this problem, verbal autopsy (VA) has gained prominence as a strategy for obtaining Cause of Death (COD) information in populations where CRVS are absent. This study reviewed publications that investigated the validation of VA methods for assessment of COD. A MEDLINE PubMed search was undertaken in June 2018 for studies published in English that investigated the validation of VA methods in sub-Saharan Africa from 1990-2018. Of the 17 studies identified, 9 fulfilled the study inclusion criteria from which additional five relevant studies were found by reviewing their references. The result showed that Physician-Certified Verbal Autopsy (PCVA) was the most widely used VA method. Validation studies comparing PCVA to hospital records, expert algorithm and InterVA demonstrated mixed and highly varied outcomes. The accuracy and reliability of the VA methods depended on level of healthcare the respondents have access to and the knowledge of the physicians on the local disease aetiology and epidemiology. As the countries in sub-Saharan Africa continue to battle with dysfunctional CRVS system, VA will remain the only viable option for the supply of child mortality data necessary for policy making. © Chigozie Jesse Uneke et al.Entities:
Keywords: Verbal autopsy; child mortality; sub-Saharan Africa; validation
Mesh:
Year: 2019 PMID: 31692720 PMCID: PMC6815483 DOI: 10.11604/pamj.2019.33.318.16405
Source DB: PubMed Journal: Pan Afr Med J
Profile of scientific publications in 2010-2018 that investigated verbal autopsy validation in sub-Saharan Africa
| Author/year/reference | Country | Target population | Study design | Scope of validation | Evidence generated | Policy implication |
|---|---|---|---|---|---|---|
| Adewemimo | Nigeria | Newborn (1-27 days), children 1-59 months and under five | Prospective | Assessment of level of agreement between the EAVA and PCVA. All-cause mortality rates calculated from NDHS by applying VASA mortality fractions to NDHS all-cause rates. | EAVA and PCVA are very useful in providing direct estimates of the causes and determinants of neonatal and 1–59month mortality. | Data generated by EAVA and PCVA can serve to help guide the improvement of maternal, neonatal and child health policies and intervention programs |
| Mpimbaza | Uganda | Newborn (1-27 days) and children 1-59 months | Prospective | Evaluation of intra-rater reliability of PCVA. Also compared the accuracy of PCVA, Non-hierarchical and hierarchical algorithm in relation to the hospital diagnosis | High intra-rater reliability (83% agreement). PCVA had high specificity for neonatal (>67%) and child death (>83%). Hierarchical was better than the non-hierarchical algorithm | PCVA remains a reliable method for determining cause of death, with high repeatability. |
| Kalter | Niger | Newborn (1-27 days) and children 1-59 months | Retrospective | Compared PCVA with expert algorithm | Both had similar neonatal death cause distribution with Sepsis, Birth asphyxia, Pneumonia ranked highest. Cause distribution for child death differ between both methods. | Reasonable agreement was found between expert algorithm and PCVA. |
| Ndila | Kenya | Children 28 days to 14 years | Retrospective | PCVA and InterVA-4 was validated against diagnosis. | 6% & 5% of deaths were attributed to SCDusing PCVA and InterVA respectively. Agreement coefficient for SCD between PCVA and hospital diagnosis was 95.5% while that for InterVAis 96.9% | VA may be useful in quantifying the contribution of SCD to childhood mortality in rural African communities. |
| Mpimbaza | Uganda | Newborn (1-27 days) and children 1-59 months | Prospective | Compared PCVA with hospital diagnosis | Sensitivity of VA in determining malaria death was 61% in Tororo and 50% in Kampala, its specificity was >88% in both locations. Its PPV varied widely between the two locations; 83% and 34% respectively. | VA provides acceptable level of accuracy for determining malaria deathat the population level in the setting of high and medium transmission. |
| Oti | Kenya | Children <5years | Retrospective | Compared InterVA and PCVA | The level of agreement between individual causes of death assigned by both methods was only 35% (kappa = 0.27, 95% CI: 0.25 - 0.30). | InterVA model showed promising results as a community-level tool for generating cause of death data from VAs |
PCVA= physician certified verbal autopsy; VASA= verbal/social autopsy; VA= verbal autopsy, EAVA= expert algorithms verbal autopsy
SCD= sickle cell disease; InterVA= computer models to facilitate interpreting verbal autopsy; NDHS= national demographic health survey
Profile of scientific publications in 2000-2009 that investigated verbal autopsy validation in sub-Saharan Africa
| Author/year/reference | Country | Target population | Study design | Scope of validation | Evidence generated | Policy implication |
|---|---|---|---|---|---|---|
| Edmond | Ghana | Newborn (1-27 days) | Prospective | Compared PCVA with hospital diagnosis | VA performed poorly in stillbirth diagnosis. For neonatal deaths, its sensitivity was >60% for major causes of death while its specificity is 76% for Birth asphyxia but >85% for prematurity and infection. | Diagnostic accuracy of VA tool should be assessed in other regions and in multicenter studies. |
| Setel | Tanzania | Perinatal, newborn and under-5 children | Prospective | Compared PCVA with hospital diagnosis | VA underestimated stillbirth and overestimated malaria death in post newborn. No other significant differences between hospital diagnosis and VA. | VA reliably estimated CSMF for diseases of public health importance. |
| Fantahun | Ethiopia | Infants <1year and children 1-14years | Prospective | Compared result of InterVA with PCVA | Both showed prematurity/low birth weight, perinatal causes and pneumonia/sepsis as the major cause of death in infants; whereas, for the older children are pneumonia/sepsis, diarrheal diseases/malnutrition and malaria. | Compared with the PCVA, InterVA model is much less tedious and yet offers 100% consistency. |
| Kahn | South Africa | Under-5 children and Adults >15years | Retrospective | Compared PCVA with hospital diagnosis | No significant difference seen between them. For communicable diseases, VA had sensitivity, specificity and PPV of 69%, 96% and 90% respectively whereas for non-communicable diseases the values were 75%, 91% and 86% respectively | Evidence showed that VA is reliable. However, needs to be validated. |
PCVA= physician certified verbal autopsy; VA= verbal autopsy; CSMFs=cause-specific mortality fractions; InterVA= computer models to facilitate interpreting verbal autopsy
CSMF= cause specific mortality fraction; PPV= positive predictive value
Profile of scientific publications in 1990-1999 that investigated verbal autopsy validation in sub-Saharan Africa
| Author/year/reference | Country | Target population | Study design | Scope of validation | Evidence generated | Policy implication |
|---|---|---|---|---|---|---|
| Quigley | Kenya | U5 children | prospective | Cause of death assessed by expert and data-derived algorithms and both were compared with hospital diagnosis | Data-derived diagnostic algorithm can give comparable or better diagnostic accuracy than expert algorithm. However, both gave high specificity. | Logistics regression and other methods for deriving algorithm should be explored in a wider setting. |
| Mobley | Namibia | U5 children | Retrospective | Compared VA diagnosis to hospital diagnosis | The sensitivities and specificities for the 5 causes of death studied were: malnutrition 73% and 76%, cerebral malaria 72% and 85%, malaria 45% and 87%, diarrhea 89% and 61%, Cough with dyspnea 72% and 64%, measles 71% and 85%. | VA can be useful in ascertaining the leading cause of death in childhood. |
| Nykanen | Malawi | Children | Retrospective | Compared VA diagnosis to hospital diagnosis | High sensitivity and specificity for the most common cause of childhood death. | VA is a promising method for collecting population-based information about child mortality |
| Todd | Gambia | Children | Retrospective | VAs were reassessed by the same Physicians and diagnosis compared. Also VA diagnosis was compared to hospital diagnosis | In 38 out of 141 VAs assessed the first and subsequent diagnosis differed, 44 out 94 diagnosis matched with the hospital diagnosis. | Poor sensitivity and specificity of VA here is due to the effect of malaria which presents like other causes. |
| Snow | Kenya | Children | Prospective | Compared PCVA diagnosis to hospital diagnosis | VA detected the common cause of death with specificities >80%. Its sensitivity for measles, neonatal tetanus, malnutrition trauma-related deaths was >75% but <50% for malaria, anemia, acute respiratory tract infection, gastroenteritis and meningitis. | VA used in malaria-specific interventions should be interpreted with caution. |
PCVA= physician certified verbal autopsy; VA= verbal autopsy