Evaluating patient data quality in South Africa’s National Health Laboratory Service Data Warehouse, 2017-2020: implications for monitoring child health programmes

Abstract Background South Africa’s National Health Laboratory Service (NHLS), the only clinical laboratory service in the country’s public health sector, is an important resource for monitoring public health programmes. Objectives We describe NHLS data quality, particularly patient demographics amon...

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Main Authors: Lebohang Radebe, Ahmad Haeri Mazanderani, Gayle G. Sherman
Format: Article
Language:English
Published: BMC 2022-06-01
Series:BMC Public Health
Subjects:
Online Access:https://doi.org/10.1186/s12889-022-13508-y
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author Lebohang Radebe
Ahmad Haeri Mazanderani
Gayle G. Sherman
author_facet Lebohang Radebe
Ahmad Haeri Mazanderani
Gayle G. Sherman
author_sort Lebohang Radebe
collection DOAJ
description Abstract Background South Africa’s National Health Laboratory Service (NHLS), the only clinical laboratory service in the country’s public health sector, is an important resource for monitoring public health programmes. Objectives We describe NHLS data quality, particularly patient demographics among infants, and the effect this has on linking multiple test results to a single patient. Methods Retrospective descriptive analysis of NHLS data from 1st January 2017—1st September 2020 was performed. A validated probabilistic record-linking algorithm linked multiple results to individual patients in lieu of a unique patient identifier. Paediatric HIV PCR data was used to illustrate the effect on monitoring and evaluating a public health programme. Descriptive statistics including medians, proportions and inter quartile ranges are reported, with Chi-square univariate tests for independence used to determine association between variables. Results During the period analysed, 485 300 007 tests, 98 217 642 encounters and 35 771 846 patients met criteria for analysis. Overall, 15.80% (n = 15 515 380) of all encounters had a registered national identity (ID) number, 2.11% (n = 2 069 785) were registered without a given name, 63.15% (n = 62 020 107) were registered to women and 32.89% (n = 32 304 329) of all folder numbers were listed as either the patient’s date of birth or unknown. For infants tested at < 7 days of age (n = 2 565 329), 0.099% (n = 2 534) had an associated ID number and 48.87% (n = 1 253 620) were registered without a given name. Encounters with a given name were linked to a subsequent encounter 40.78% (n = 14 180 409 of 34 775 617) of the time, significantly more often than the 21.85% (n = 217 660 of 996 229) of encounters registered with a baby-derivative name (p-value < 0.001). Conclusion Unavailability and poor capturing of patient demographics, especially among infants and children, affects the ability to accurately monitor routine health programmes. A unique national patient identifier, other than the national ID number, is urgently required and must be available at birth if South Africa is to accurately monitor programmes such as the Prevention of Mother-to-Child Transmission of HIV.
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spelling doaj.art-4923ecaa1d514fef9d2a06cd37daaa502022-12-22T01:20:55ZengBMCBMC Public Health1471-24582022-06-0122111010.1186/s12889-022-13508-yEvaluating patient data quality in South Africa’s National Health Laboratory Service Data Warehouse, 2017-2020: implications for monitoring child health programmesLebohang Radebe0Ahmad Haeri Mazanderani1Gayle G. Sherman2Centre for HIV and STIs, National Institute for Communicable Diseases, National Health Laboratory ServiceCentre for HIV and STIs, National Institute for Communicable Diseases, National Health Laboratory ServiceCentre for HIV and STIs, National Institute for Communicable Diseases, National Health Laboratory ServiceAbstract Background South Africa’s National Health Laboratory Service (NHLS), the only clinical laboratory service in the country’s public health sector, is an important resource for monitoring public health programmes. Objectives We describe NHLS data quality, particularly patient demographics among infants, and the effect this has on linking multiple test results to a single patient. Methods Retrospective descriptive analysis of NHLS data from 1st January 2017—1st September 2020 was performed. A validated probabilistic record-linking algorithm linked multiple results to individual patients in lieu of a unique patient identifier. Paediatric HIV PCR data was used to illustrate the effect on monitoring and evaluating a public health programme. Descriptive statistics including medians, proportions and inter quartile ranges are reported, with Chi-square univariate tests for independence used to determine association between variables. Results During the period analysed, 485 300 007 tests, 98 217 642 encounters and 35 771 846 patients met criteria for analysis. Overall, 15.80% (n = 15 515 380) of all encounters had a registered national identity (ID) number, 2.11% (n = 2 069 785) were registered without a given name, 63.15% (n = 62 020 107) were registered to women and 32.89% (n = 32 304 329) of all folder numbers were listed as either the patient’s date of birth or unknown. For infants tested at < 7 days of age (n = 2 565 329), 0.099% (n = 2 534) had an associated ID number and 48.87% (n = 1 253 620) were registered without a given name. Encounters with a given name were linked to a subsequent encounter 40.78% (n = 14 180 409 of 34 775 617) of the time, significantly more often than the 21.85% (n = 217 660 of 996 229) of encounters registered with a baby-derivative name (p-value < 0.001). Conclusion Unavailability and poor capturing of patient demographics, especially among infants and children, affects the ability to accurately monitor routine health programmes. A unique national patient identifier, other than the national ID number, is urgently required and must be available at birth if South Africa is to accurately monitor programmes such as the Prevention of Mother-to-Child Transmission of HIV.https://doi.org/10.1186/s12889-022-13508-yUnique patient identifierData qualityMonitoring and evaluationPublic health programmesEarly infant HIV diagnosis
spellingShingle Lebohang Radebe
Ahmad Haeri Mazanderani
Gayle G. Sherman
Evaluating patient data quality in South Africa’s National Health Laboratory Service Data Warehouse, 2017-2020: implications for monitoring child health programmes
BMC Public Health
Unique patient identifier
Data quality
Monitoring and evaluation
Public health programmes
Early infant HIV diagnosis
title Evaluating patient data quality in South Africa’s National Health Laboratory Service Data Warehouse, 2017-2020: implications for monitoring child health programmes
title_full Evaluating patient data quality in South Africa’s National Health Laboratory Service Data Warehouse, 2017-2020: implications for monitoring child health programmes
title_fullStr Evaluating patient data quality in South Africa’s National Health Laboratory Service Data Warehouse, 2017-2020: implications for monitoring child health programmes
title_full_unstemmed Evaluating patient data quality in South Africa’s National Health Laboratory Service Data Warehouse, 2017-2020: implications for monitoring child health programmes
title_short Evaluating patient data quality in South Africa’s National Health Laboratory Service Data Warehouse, 2017-2020: implications for monitoring child health programmes
title_sort evaluating patient data quality in south africa s national health laboratory service data warehouse 2017 2020 implications for monitoring child health programmes
topic Unique patient identifier
Data quality
Monitoring and evaluation
Public health programmes
Early infant HIV diagnosis
url https://doi.org/10.1186/s12889-022-13508-y
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