MANAGEMENT OF NOROVIRUS INFECTION IN SOLID ORGAN TRANSPLANT RECIPIENTS: A SCOPING REVIEW

 

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https://storage.unitedwebnetwork.com/files/1099/1eacc7531449e79c542f00ea0c80e7c4.pdf
MANAGEMENT OF NOROVIRUS INFECTION IN SOLID ORGAN TRANSPLANT RECIPIENTS: A SCOPING REVIEW

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Thida
Maung Myint
Thida Maung Myint Thida.Myint1@health.nsw.gov.au John Hunter Hospital Renal Dept Newcastle Australia *
Jonathan Hand jonathan.hand@ochsner.org The University of Queensland Medical School - Ochsner Health Ochsner Health Louisiana United States -
Adam Lowe alo5603@gmail.com The University of Queensland Medical School - Ochsner Health Ochsner Health Louisiana United States -
Camille N Kotton CKOTTON@mgh.harvard.edu Massachusetts General Hospital, Harvard Medical School, Transplant and Immunocompromised Host Service, Infectious Diseases Division Boston, MA United States -
Sharon C-A Chen Sharon.Chen@health.nsw.gov.au Sydney Infectious Diseases Institute The University of Sydney Sydney Australia -
Justin Beardsley Justin.Beardsley@health.nsw.gov.au Institute of Clinical Pathology and Medical Research Centre for Infectious Diseases and Microbiology Laboratory Services, Institute of Clinical Pathology and Medical Research Sydney Australia -
Armando Teixeira-Pinto armando.teixeira-pinto@sydney.edu.au Centre for Kidney Research The Children’s Hospital at Westmead Sydney Australia -
Germaine Wong germaine.wong@health.nsw.gov.au Centre for Kidney Research The Children’s Hospital at Westmead Sydney Australia -
Samuel Chan samuel.chan@newmedschool.com.au New Medical Education Australia Pty Ltd New Medical Education Brisbane Australia -
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Norovirus infection causes significant morbidity in solid organ transplant (SOT) recipients, yet few treatments are available and evidence for efficacy is sparse. In this scoping review, we identify and evaluate potential interventions for managing norovirus infections in SOT recipients.

We searched electronic databases from inception to 6th July 2025. Eligible studies were analyzed for participants’ characteristics, intervention types and reported outcomes.

After screening 245 abstracts, 57 studies were included (one randomized controlled trial (RCT), 27 cohort studies, 5 case series and 24 case reports), mainly from the United States (US). Transplant types included kidney (n=36), liver (n=12), cardiac (n=12), pulmonary (n=7), pancreas (n=6), small bowel (n=7), and multiorgan (n=13) transplants. The most frequently reported primary outcome was resolution of gastrointestinal (GI) symptoms. Interventions were diverse: immunosuppression modification (n=14), nitazoxanide (n=6), intravenous immunoglobulin (IVIG) (n=3), oral immunoglobulin (n=9), combination of these (n=19), faecal transplant (n=2), supportive management (n=4), and others not classified (n=5). Limited quality evidence for positive clinical outcomes was reported for immunosuppression modification (n=6/13), nitazoxanide (n=4/6), IVIG (n=2/3), oral immunoglobulin alone (n=9/9), faecal transplant (n=2/2), supportive treatment (n=4/4), and a combination of treatments (n=11/19). A lack of clinical improvement was described in 13 of 57 studies.

Table 1. Study characteristics (n=57)

Study characteristics

Value 

Publication year, n (%)

 

Before 2000

0

2000-2009

3 (5)

2010-2019

29 (51)

2020 onwards

25 (44)

Study type, n (%)

 

RCT

1 (2)

Cohort

 

Prospective 

6 (11)

Retrospective 

21(37)

Case series 

5 (9)

Case reports 

24 (42)

Sample size, n (%)

 

0-9

32 (56)

10-49

10 (18)

50-99

7 (12)

100-199

7 (12)

>200

1 (2)

Population subgroups, n (%)

 

Adults

44 (77)

Children 

13 (13)

Type of transplant, n (%)

 

Kidney transplant alone 

28 (49)

Solid organ transplants including kidney, heart, lung, liver intestine and combined multiple transplants

36 (63)

Solid organ transplants and others (haemopoietic stem cell transplants, immunosuppressed patients including haematological malignancies and solid tumours)

3 (5)

Interventions*, n (%)

 

Immunosuppressive therapy modification alone  

14 (25)

Nitazoxanide alone 

6 (11)

Intravenous immunoglobulin therapy alone

3 (5)

Oral immunoglobulin therapy alone n 

9 (16)

Combination of treatments

17 (30)

Faecal microbiota transplant 

2 (4)

Supportive management

4 (7)

Others 

5 (9)

Reported outcomes, n (%)

 

Improvement in GI symptoms

38 (67)

Improvement of extra-GI symptoms

2 (4)

Reporting of graft-related outcomes (stable function/rejection)

8 (14)

Evidence of eradication of norovirus in stool

3 (5)

No/minimal improvement in symptoms

13 (23)

Reporting of adverse drug reactions

1 (2)

* One study was conducted with multiple treatment arms.

Figure 1 and 2 included as follows.

Figure 1. Flow diagram depicting the inclusion and exclusion of various studies


Figure 2. The reporting characteristics across the different  studies

A wide range of interventions has been used to manage norovirus infections in SOT recipients; however, the evidence is limited to observational studies, and the findings are uncertain. High-quality RCTs are needed to establish treatment efficacy and safety.  

Kewords