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Improving timeliness of hepatitis B vaccine administration in an urban safety net level III NICU.
Hayashi, Madoka; Grover, Theresa R; Small, Steve; Staples, Tessa; Roosevelt, Genie.
Afiliação
  • Hayashi M; Department of Pediatrics, Denver Health and Hospital Authority, Denver, CO, USA madoka.hayashi@dhha.org.
  • Grover TR; Department of Pediatrics, Section of Neonatology, University of Colorado School of Medicine, Aurora, CO, USA.
  • Small S; Department of Pediatrics, Section of Neonatology, Children's Hospital Colorado, Aurora, CO, USA.
  • Staples T; Department of Pediatrics, Section of Neonatology, University of Colorado School of Medicine, Aurora, CO, USA.
  • Roosevelt G; Department of Pediatrics, Section of Neonatology, Children's Hospital Colorado, Aurora, CO, USA.
BMJ Qual Saf ; 30(11): 911-919, 2021 11.
Article em En | MEDLINE | ID: mdl-34001649
ABSTRACT

OBJECTIVE:

To avoid preventable consequences of perinatal hepatitis B infection, all infants should be given hepatitis B vaccine (HBV) within 24 hours of birth if birth weight is ≥2 kg and at 30 days of life or at discharge if <2 kg, to provide highest seroprotection rates while ensuring universal vaccination prior to discharge. We aimed to achieve timely HBV administration in >80% of eligible infants in both birthweight groups and decrease infants discharged home without receiving HBV to <1% over an 18-month period and sustain results for an additional 15 months.

METHODS:

Data were collected from June 2016 to May 2020 in a level III neonatal intensive care unit. A multidisciplinary team identified barriers and interventions through Plan-Do-Study-Act cycles from September 2017 to February 2019 using pharmacists as champions, overcoming legal barriers, staff education and best practice alerts (BPAs) embedded in electronic health records. Statistical process control (SPC) p charts were used to evaluate the primary outcome measure, monthly percentage of infants receiving timely HBV administration stratified by birthweight categories (≥2 and <2 kg). For infants receiving HBV outside the time frame, absolute difference of timeliness was calculated.

RESULTS:

Mean timely HBV administration improved from 45% to 95% (≥2 kg) and from 45% to 85% (<2 kg) with special cause variation in SPC charts. Infants discharged without receiving HBV decreased from 4.6% to 0.22%. Of those given HBV outside the recommended time frame, median absolute time between recommended and actual administration time decreased significantly from 3.5 days (IQR 1.6, 8.6) to 0.3 day (IQR 0.1, 0.8) (p<0.001) in ≥2 kg group and from 6 days (IQR 1, 15) to 1 day (IQR 1, 6.5) (p=0.009) in <2 kg group.

CONCLUSIONS:

Using a multidisciplinary approach, we significantly improved and sustained timely HBV administration and nearly eliminated infants discharged home without receiving HBV. Pharmacists as champions and BPAs were critical to our success.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vacinas contra Hepatite B / Hepatite B Tipo de estudo: Guideline Limite: Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: BMJ Qual Saf Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vacinas contra Hepatite B / Hepatite B Tipo de estudo: Guideline Limite: Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: BMJ Qual Saf Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos