Using Quality Improvement to Implement a Standardized Approach to Neonatal Herpes Simplex Virus

Author:

Brower Laura H.12,Wilson Paria M.2345,Murtagh Kurowski Eileen236,Haslam David27,Courter Joshua8,Goyal Neera12910,Durling Michelle1,Shah Samir S.1267,Schondelmeyer Amanda126

Affiliation:

1. Divisions of Hospital Medicine,

2. Department of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, Ohio;

3. Pediatric Emergency Medicine,

4. Division of Pediatric Emergency Medicine, Children’s Hospital of Pittsburgh, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania;

5. Department of Pediatrics, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania;

6. James M. Anderson Center for Health Systems Excellence, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio

7. Infectious Diseases, and

8. Pharmacy, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio;

9. Division of External Primary Care, Nemours/Alfred I duPont Hospital for Children, Wilmington, Delaware;

10. Department of Pediatrics, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania; and

Abstract

OBJECTIVES: Neonatal herpes simplex virus (HSV) infections are associated with high mortality and long-term morbidity. However, incidence is low and acyclovir, the treatment of choice, carries risk of toxicity. We aimed to increase the percentage of patients 0 to 60 days of age who are tested and treated for HSV in accordance with local guideline recommendations from 40% to 80%. METHODS: This quality improvement project took place at 1 freestanding children’s hospital. Multiple plan-do-study-act cycles were focused on interventions aimed at key drivers including provider buy-in, guideline availability, and accurate identification of high-risk patients. A run chart was used to track the effect of interventions on the percentage managed per guideline recommendations over time by using established rules for determining special cause. Pre- and postimplementation acyclovir use was compared by using a χ2 test. In HSV-positive cases, delayed acyclovir initiation, defined as >1 day from presentation, was tracked as a balancing measure. RESULTS: The median percentage of patients managed according to guideline recommendations increased from 40% to 80% within 8 months. Acyclovir use decreased from 26% to 7.9% (P < .001) in non–high-risk patients but did not change significantly in high-risk patients (73%–83%; P = .15). There were no cases of delayed acyclovir initiation in HSV-positive cases. CONCLUSIONS: Point-of-care availability of an evidence-based guideline and interventions targeted at provider engagement improved adherence to a new guideline for neonatal HSV management and decreased acyclovir use in non–high-risk infants. Further study is necessary to confirm the safety of these recommendations in other settings.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology, and Child Health

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