Why parents refuse newborn hearing screening and default on follow-up rescreening : a South African perspective

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dc.contributor.author Scheepers, Lucia Jane
dc.contributor.author Swanepoel, De Wet
dc.contributor.author Le Roux, Talita
dc.date.accessioned 2014-07-15T08:46:15Z
dc.date.available 2014-07-15T08:46:15Z
dc.date.issued 2014-04
dc.description.abstract OBJECTIVES : This study describes screen refusal and follow-up default characteristics together with caregiver reasons for screen refusal and follow-up default in two South African universal newborn hearing screening programs. METHODS : A retrospective record review of universal newborn hearing screening conducted at two hospitals (Hospital A n = 954 infants; Hospital B n = 2135) over a 31–33 month period. Otoacoustic emission screening was conducted with rescreen recommended within six weeks for a uni- or bilateral refer. Program efficacy was described according to coverage, referral and follow-up rates. A prospective telephonic interview with caregivers who declined the initial screen (n = 25) and who defaulted on follow-up (n = 25) constituted the next study component. Caregivers were randomly selected from the screening programs for a survey related to reasons for newborn hearing screening refusal and follow-up default. RESULTS : Screening coverage (89.3% Hospital A; 57.4% Hospital B), initial referral rates (11.6% Hospital A; 21.2% Hospital B) and follow-up return rates (56.1% Hospital A; 35.8% Hospital B) differed significantly between hospitals and were below benchmarks. The most frequent reasons for screen refusal were related to costs (72%), caregiver knowledge of newborn hearing screening (64%) and health care professional knowledge and team collaboration (16%). Almost all caregivers (96%) indicated that if costs had been included in the birthing package or covered by medical insurance they would have agreed to newborn hearing screening. Reasons for follow-up default were most commonly related to caregiver knowledge of newborn hearing screening (32%) and costs (28%). One in four caregivers (24%) defaulted on follow-up because they forgot to bring their infant for a rescreen. Only half of caregivers (48%) who defaulted on follow-up reported being aware of initial screen results while 60% reported being aware of the recommended follow-up rescreen. CONCLUSION : Caregivers most commonly refused screening due to associated costs and mostly defaulted on follow-up due to an apparent lack of knowledge regarding initial screen outcome and recommendations made for follow-up. Including NHS as a mandated birthing service is essential if coverage is to be increased, while reducing follow-up defaults requires proactive reminders and improved communication with caregivers en_US
dc.description.librarian hb2014 en_US
dc.description.uri http://www.elsevier.com/locate/ijporl en_US
dc.identifier.citation Scheepers, LJ, Swanepoel, DW & Le Roux, T 2014, 'Why parents refuse newborn hearing screening and default on follow-up rescreening : a South African perspective', International Journal of Pediatric Otorhinolaryngology, vol. 78, no. 4, pp. 652-658. en_US
dc.identifier.issn 0165-5876 (print)
dc.identifier.issn 1872-8464 (online)
dc.identifier.other 10.1016/j.ijporl.2014.01.026
dc.identifier.uri http://hdl.handle.net/2263/40748
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.rights © 2014 Elsevier Ireland Ltd. All rights reserved. All rights reserved. Notice : this is the author’s version of a work that was accepted for publication in International Journal of Pediatric Otorhinolaryngology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in International Journal of Pediatric Otorhinolaryngology, vol. 78 , no.4, pp. 652-658, 2014. doi : 10.1016/j.ijporl.2014.01.026. en_US
dc.subject Universal newborn hearing screening en_US
dc.subject Early hearing detection and intervention en_US
dc.subject Distortion product otoacoustic emissions en_US
dc.subject Coverage en_US
dc.subject Screen refusal en_US
dc.subject Follow-up default en_US
dc.title Why parents refuse newborn hearing screening and default on follow-up rescreening : a South African perspective en_US
dc.type Postprint Article en_US


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