Factors contributing to measles transmission during an outbreak in Kamwenge District, Western Uganda, April to August 2015
dc.contributor.author | Nsubuga, Fred | |
dc.contributor.author | Bulage, Lilian | |
dc.contributor.author | Ampeire, Immaculate | |
dc.contributor.author | Matovu, Joseph K. B. | |
dc.contributor.author | Kasasa, Simon | |
dc.contributor.author | Tanifum, Patricia | |
dc.contributor.author | Riolexus, Alex Ario | |
dc.contributor.author | Zhu, Bao-Ping | |
dc.date.accessioned | 2018-07-25T12:22:50Z | |
dc.date.available | 2018-07-25T12:22:50Z | |
dc.date.issued | 2018 | |
dc.description | This article discusses in April 2015, Kamwenge District, western Uganda reported a measles outbreak. We investigated the outbreak to identify potential exposures that facilitated measles transmission, assess vaccine effectiveness (VE) and vaccination coverage (VC), and recommend prevention and control measures. | en_US |
dc.description.abstract | Background: In April 2015, Kamwenge District, western Uganda reported a measles outbreak. We investigated the outbreak to identify potential exposures that facilitated measles transmission, assess vaccine effectiveness (VE) and vaccination coverage (VC), and recommend prevention and control measures. Methods: For this investigation, a probable case was defined as onset of fever and generalized maculopapular rash, plus ≥1 of the following symptoms: Coryza, conjunctivitis, or cough. A confirmed case was defined as a probable case plus identification of measles-specific IgM in serum. For case-finding, we reviewed patients’ medical records and conducted in-home patient examination. In a case-control study, we compared exposures of case-patients Nand controls matched by age and village of residence. For children aged 9 m-5y, we estimated VC using the percent of children among the controls who had been vaccinated against measles, and calculated VE using the formula, VE = 1 - ORM-H, where ORM-H was the Mantel-Haenszel odds ratio associated with having a measles vaccination history. Results: We identified 213 probable cases with onset between April and August, 2015. Of 23 blood specimens collected, 78% were positive for measles-specific IgM. Measles attack rate was highest in the youngest age-group, 0-5y (13/10,000), and decreased as age increased. The epidemic curve indicated sustained propagation in the community. Of the 50 case-patients and 200 controls, 42% of case-patients and 12% of controls visited health centers during their likely exposure period (ORM-H = 6.1; 95% CI = 2.7–14). Among children aged 9 m-5y, VE was estimated at 70% (95% CI: 24–88%), and VC at 75% (95% CI: 67–83%). Excessive crowding was observed at all health centers; no patient triage-system existed. Conclusions: The spread of measles during this outbreak was facilitated by patient mixing at crowded health centers, suboptimal VE and inadequate VC. We recommended emergency immunization campaign targeting children <5y in the affected sub-counties, as well as triaging and isolation of febrile or rash patients visiting health centers. | en_US |
dc.identifier.citation | Nsubuga et al. Factors contributing to measles transmission during an outbreak in Kamwenge District, Western Uganda, April to August 2015. BMC Infectious Diseases Vol. 18 No. 21 (2018) DOI 10.1186/s12879-017-2941-4 | en_US |
dc.identifier.uri | https://hdl.handle.net/20.500.11951/284 | |
dc.language.iso | en | en_US |
dc.publisher | BMC Infectious Diseases | en_US |
dc.subject | Measles | en_US |
dc.subject | Vaccine effectiveness | en_US |
dc.subject | Vaccine failure | en_US |
dc.subject | Global health security | en_US |
dc.title | Factors contributing to measles transmission during an outbreak in Kamwenge District, Western Uganda, April to August 2015 | en_US |
dc.type | Article | en_US |
Files
Original bundle
1 - 1 of 1
Loading...
- Name:
- Nsubuga et al. Factors contributing to measles transmission during an outbreak in Kamwenge District. 2018.pdf
- Size:
- 434.55 KB
- Format:
- Adobe Portable Document Format
- Description:
- The final, definitive version of this paper has been published in BMC Infectious Diseases Vol. 18 No. 21 (2018). All rights reserved.
License bundle
1 - 1 of 1
No Thumbnail Available
- Name:
- license.txt
- Size:
- 1.97 KB
- Format:
- Item-specific license agreed upon to submission
- Description: