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Measles Outbreak at a Privately Operated Detention Facility: Arizona, 2016

Supporting Files
File Language:
English


Details

  • Alternative Title:
    Clin Infect Dis
  • Personal Author:
  • Description:
    Background.

    We describe a measles outbreak and control measures implemented at a privately operated detention facility housing US Immigration and Customs Enforcement detainees in 2016.

    Methods.

    Case-patients reported fever and rash and were either laboratory-confirmed or had an epidemiological link to a laboratory-confirmed case-patient. Immunoglobulin G (IgG) avidity and plaque reduction neutralization tests distinguished between primary acute and reinfection case-patients. Measles-specific IgG was measured to assess detainee immunity levels. We compared attack rates (ARs) among detainees and staff, between IgG-negative and IgG-positive detainees, and by detainee housing units and sexes.

    Results.

    We identified 32 measles case-patients (23 detainees, 9 staff); rash onsets were during 6 May–26 June 2016. High IgG avidity and neutralizing-antibody titers >40 000 to measles (indicating reinfection) were identified in 18 (95%) and 15 (84%) of 19 tested case-patients, respectively. Among 205 unit A detainees tested for presumptive immunity, 186 (91%) had detectable IgG. Overall, the AR was 1.65%. ARs were significantly higher among detainees in unit A (7.05%) compared with units B-F (0.59%), and among male (2.33%) compared with female detainees (0.38%); however, ARs were not significantly different between detainees and staff or between IgG-negative and IgG-positive detainees. Control measures included the vaccination of 1424 of 1425 detainees and 190 of 510 staff, immunity verification for 445 staff, case-patient isolation, and quarantine of affected units.

    Conclusions.

    Although ARs were low, measles outbreaks can occur in intense-exposure settings, despite a high population immunity, underscoring the importance of high vaccination coverage and containment in limiting measles transmission.

  • Subjects:
  • Source:
    Clin Infect Dis. 68(12):2018-2025
  • Pubmed ID:
    30256908
  • Pubmed Central ID:
    PMC6435422
  • Document Type:
  • Funding:
  • Volume:
    68
  • Issue:
    12
  • Collection(s):
  • Main Document Checksum:
    urn:sha256:026acbf52f2328e67a99273d4ca830fe21eabaf10619d5f5daf150405687815c
  • Download URL:
  • File Type:
    Filetype[PDF - 370.46 KB ]
File Language:
English
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