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Murine Corneal Transplantation: A Model to Study the Most Common Form of Solid Organ Transplantation
Published on: November 17, 2014
Impact of standardized protocols for cytomegalovirus disease prevention in pediatric solid organ transplant
Lakshmi Ganapathi1, Jennifer Blumenthal1,2, Laila Alawdah1
1Division of Infectious Diseases, Boston Children's Hospital, Boston, Massachusetts.
Insights
Standardized protocols improved cytomegalovirus (CMV) prevention in pediatric solid organ transplant (SOT) recipients. Appropriate prophylaxis increased, neutropenia decreased, and asymptomatic CMV DNAemia was more frequently detected and treated.
Area of Science:
- Pediatric Solid Organ Transplantation
- Infectious Disease Management
- Cytomegalovirus (CMV) Research
Background:
- Cytomegalovirus (CMV) infection poses significant risks for pediatric solid organ transplant (SOT) recipients, leading to morbidity and mortality.
- Varied practices in CMV testing, prophylaxis, and surveillance existed across SOT groups.
- Standardized, evidence-based protocols were needed to optimize CMV prevention strategies.
Purpose of the Study:
- To implement and evaluate standardized, evidence-based protocols for CMV prevention in pediatric SOT recipients.
- To assess the impact of standardized protocols on prophylaxis, neutropenia, and CMV DNAemia/disease.
- To address practice variations in CMV management within a single center.
Main Methods:
- Retrospective chart review of pediatric SOT recipients from 2009-2014 at Boston Children's Hospital.
- Descriptive statistics used to compare outcomes pre- and post-protocol implementation.
- Analysis focused on prophylaxis provision, neutropenia, CMV DNAemia, and CMV disease occurrence.
Main Results:
- Appropriate valganciclovir prophylaxis improved across most SOT groups post-intervention (P < .01).
- Recurrent neutropenia episodes decreased significantly post-intervention (30% vs 10%, P < .001).
- CMV disease incidence remained low and unchanged, but asymptomatic CMV DNAemia detection and treatment increased.
Conclusions:
- Implementation of standardized CMV prevention protocols enhanced appropriate prophylaxis delivery.
- Protocols led to increased diagnosis and treatment of asymptomatic CMV DNAemia.
- Standardized protocols effectively reduced recurrent neutropenia in pediatric SOT patients receiving prophylaxis.
Abstract:
End-organ disease caused by CMV is a significant cause of morbidity and mortality in pediatric SOT recipients. Pediatric transplant centers have adopted various approaches for CMV disease prevention in this patient population. We observed significant practice variation in CMV testing, prophylaxis, and surveillance across SOT groups in our center. To address this, we implemented evidence-based standardized protocols and measured outcomes pre- and post-implementation of these protocols. We performed retrospective chart review for SOT recipients from 2009 to 2014 at Boston Children's Hospital. Using descriptive statistics, we measured practice improvement in provision of appropriate prophylaxis, occurrence of neutropenia and associated complications, and occurrence of CMV DNAemia and CMV disease pre- and post-intervention. The pre- and post-intervention periods included 141 and 109 patients, respectively. With the exception of kidney transplant recipients, provision of appropriate valganciclovir prophylaxis improved across SOT groups post-intervention (P < .01). Occurrence of >1 episode of neutropenia was greater in the preintervention period (30% vs 10%, P < .001). In both periods, neutropenia was associated with few episodes of invasive infections. The occurrence of CMV disease did not differ and was overall low. However, due to routine surveillance a significantly greater number of asymptomatic CMV DNAemia episodes were identified and treated in the post-intervention period. Implementation of standardized prevention protocols helped to improve the provision of appropriate prophylaxis to patients at risk for CMV acquisition, increased the diagnosis and treatment of asymptomatic CMV DNAemia, and decreased episodes of recurrent neutropenia in patients receiving prophylaxis.
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