dc.contributor.author |
Wolpaw, Benjamin
|
en_ZA |
dc.contributor.author |
Mathews, Catherine
|
en_ZA |
dc.contributor.author |
Chopra, Mickey
|
en_ZA |
dc.contributor.author |
Hardie, Diana
|
en_ZA |
dc.contributor.author |
de Azevedo, Virginia
|
en_ZA |
dc.contributor.author |
Jennings, Karen
|
en_ZA |
dc.contributor.author |
Lurie, Mark
|
en_ZA |
dc.date.accessioned |
2015-10-28T07:09:15Z |
|
dc.date.available |
2015-10-28T07:09:15Z |
|
dc.date.issued |
2010 |
en_ZA |
dc.identifier.citation |
Wolpaw, B. J., Mathews, C., Chopra, M., Hardie, D., de Azevedo, V., Jennings, K., & Lurie, M. N. (2010). The failure of routine rapid HIV testing: a case study of improving low sensitivity in the field. BMC health services research, 10(1), 73. |
en_ZA |
dc.identifier.uri |
http://hdl.handle.net/11427/14482
|
|
dc.identifier.uri |
http://dx.doi.org/10.1186/1472-6963-10-73
|
|
dc.description.abstract |
BACKGROUND:The rapid HIV antibody test is the diagnostic tool of choice in low and middle-income countries. Previous evidence suggests that rapid HIV diagnostic tests may underperform in the field, failing to detect a substantial number of infections. A research study inadvertently discovered that a clinic rapid HIV testing process was failing to detect cases of established (high antibody titer) infection, exhibiting an estimated 68.7% sensitivity (95% CI [41.3%-89.0%]) over the course of the first three weeks of observation. The setting is a public service clinic that provides STI diagnosis and treatment in an impoverished, peri-urban community outside of Cape Town, South Africa. METHODS: The researchers and local health administrators collaborated to investigate the cause of the poor test performance and make necessary corrections. The clinic changed the brand of rapid test being used and later introduced quality improvement measures. Observations were made of the clinic staff as they administered rapid HIV tests to real patients. Estimated testing sensitivity was calculated as the number of rapid HIV test positive individuals detected by the clinic divided by this number plus the number of PCR positive, highly reactive 3rd generation ELISA patients identified among those who were rapid test negative at the clinic. RESULTS: In the period of five months after the clinic made the switch of rapid HIV tests, estimated sensitivity improved to 93.5% (95% CI [86.5%-97.6%]), during which time observations of counselors administering tests at the clinic found poor adherence to the recommended testing protocol. Quality improvement measures were implemented and estimated sensitivity rose to 95.1% (95% CI [83.5%-99.4%]) during the final two months of full observation. CONCLUSIONS: Poor testing procedure in the field can lead to exceedingly low levels of rapid HIV test sensitivity, making it imperative that stringent quality control measures are implemented where they do not already exist. Certain brands of rapid-testing kits may perform better than others when faced with sub-optimal use. |
en_ZA |
dc.language.iso |
eng |
en_ZA |
dc.publisher |
BioMed Central Ltd |
en_ZA |
dc.rights |
This is an open access article distributed under the terms of the Creative Commons Attribution License |
en_ZA |
dc.rights.uri |
http://creativecommons.org/licenses/by/2.0 |
en_ZA |
dc.source |
BMC Health Services Research |
en_ZA |
dc.source.uri |
http://www.biomedcentral.com/bmchealthservres/
|
en_ZA |
dc.subject.other |
HIV Infections |
en_ZA |
dc.subject.other |
Mass Screening |
en_ZA |
dc.subject.other |
Quality Control |
en_ZA |
dc.subject.other |
Reagent Kits, Diagnostic |
en_ZA |
dc.title |
The failure of routine rapid HIV testing: a case study of improving low sensitivity in the field |
en_ZA |
dc.type |
Journal Article |
en_ZA |
dc.rights.holder |
2010 Wolpaw et al; licensee BioMed Central Ltd. |
en_ZA |
uct.type.publication |
Research |
en_ZA |
uct.type.resource |
Article
|
en_ZA |
dc.publisher.institution |
University of Cape Town |
|
dc.publisher.faculty |
Faculty of Health Sciences |
en_ZA |
dc.publisher.department |
Department of Public Health and Family Medicine |
en_ZA |
uct.type.filetype |
Text |
|
uct.type.filetype |
Image |
|
dc.identifier.apacitation |
Wolpaw, B., Mathews, C., Chopra, M., Hardie, D., de Azevedo, V., Jennings, K., & Lurie, M. (2010). The failure of routine rapid HIV testing: a case study of improving low sensitivity in the field. <i>BMC Health Services Research</i>, http://hdl.handle.net/11427/14482 |
en_ZA |
dc.identifier.chicagocitation |
Wolpaw, Benjamin, Catherine Mathews, Mickey Chopra, Diana Hardie, Virginia de Azevedo, Karen Jennings, and Mark Lurie "The failure of routine rapid HIV testing: a case study of improving low sensitivity in the field." <i>BMC Health Services Research</i> (2010) http://hdl.handle.net/11427/14482 |
en_ZA |
dc.identifier.vancouvercitation |
Wolpaw B, Mathews C, Chopra M, Hardie D, de Azevedo V, Jennings K, et al. The failure of routine rapid HIV testing: a case study of improving low sensitivity in the field. BMC Health Services Research. 2010; http://hdl.handle.net/11427/14482. |
en_ZA |
dc.identifier.ris |
TY - Journal Article
AU - Wolpaw, Benjamin
AU - Mathews, Catherine
AU - Chopra, Mickey
AU - Hardie, Diana
AU - de Azevedo, Virginia
AU - Jennings, Karen
AU - Lurie, Mark
AB - BACKGROUND:The rapid HIV antibody test is the diagnostic tool of choice in low and middle-income countries. Previous evidence suggests that rapid HIV diagnostic tests may underperform in the field, failing to detect a substantial number of infections. A research study inadvertently discovered that a clinic rapid HIV testing process was failing to detect cases of established (high antibody titer) infection, exhibiting an estimated 68.7% sensitivity (95% CI [41.3%-89.0%]) over the course of the first three weeks of observation. The setting is a public service clinic that provides STI diagnosis and treatment in an impoverished, peri-urban community outside of Cape Town, South Africa. METHODS: The researchers and local health administrators collaborated to investigate the cause of the poor test performance and make necessary corrections. The clinic changed the brand of rapid test being used and later introduced quality improvement measures. Observations were made of the clinic staff as they administered rapid HIV tests to real patients. Estimated testing sensitivity was calculated as the number of rapid HIV test positive individuals detected by the clinic divided by this number plus the number of PCR positive, highly reactive 3rd generation ELISA patients identified among those who were rapid test negative at the clinic. RESULTS: In the period of five months after the clinic made the switch of rapid HIV tests, estimated sensitivity improved to 93.5% (95% CI [86.5%-97.6%]), during which time observations of counselors administering tests at the clinic found poor adherence to the recommended testing protocol. Quality improvement measures were implemented and estimated sensitivity rose to 95.1% (95% CI [83.5%-99.4%]) during the final two months of full observation. CONCLUSIONS: Poor testing procedure in the field can lead to exceedingly low levels of rapid HIV test sensitivity, making it imperative that stringent quality control measures are implemented where they do not already exist. Certain brands of rapid-testing kits may perform better than others when faced with sub-optimal use.
DA - 2010
DB - OpenUCT
DO - 10.1186/1472-6963-10-73
DP - University of Cape Town
J1 - BMC Health Services Research
LK - https://open.uct.ac.za
PB - University of Cape Town
PY - 2010
T1 - The failure of routine rapid HIV testing: a case study of improving low sensitivity in the field
TI - The failure of routine rapid HIV testing: a case study of improving low sensitivity in the field
UR - http://hdl.handle.net/11427/14482
ER -
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en_ZA |