Respiratory syncytial virus: Difference between revisions
From IDWiki
m (Text replacement - "Clinical Presentation" to "Clinical Manifestations") |
m (→) |
||
(3 intermediate revisions by the same user not shown) | |||
Line 1: | Line 1: | ||
== Background == |
== Background == |
||
=== Microbiology === |
=== Microbiology === |
||
* Single-stranded, enveloped RNA virus in the Pneumoviridae subfamily of the Paramyxoviridae family |
* Single-stranded, enveloped RNA virus in the [[Family::Pneumoviridae]] subfamily of the Paramyxoviridae family |
||
* Two antigenic groups, A and B |
* Two antigenic groups, A and B |
||
Line 13: | Line 13: | ||
== Clinical Manifestations == |
== Clinical Manifestations == |
||
* Incubation period of 3 to 5 days (up to 8) |
* Incubation period of [[Usual incubation period::3 to 5 days]] ([[Incubation period range::up to 8 days]]) |
||
=== Children === |
=== Children === |
||
Line 24: | Line 24: | ||
* Hypoxia necessitates hospitalization, and may fluctuate, and can also have apnea |
* Hypoxia necessitates hospitalization, and may fluctuate, and can also have apnea |
||
==== Outcomes and |
==== Outcomes and Sequelae ==== |
||
* Cough may last for 4 or more weeks, despite resolution of the infection |
* Cough may last for 4 or more weeks, despite resolution of the infection |
||
* Recurrent infections are common |
* Recurrent infections are common |
||
Line 32: | Line 32: | ||
* More common in people who work with children and military recruits living in barracks |
* More common in people who work with children and military recruits living in barracks |
||
* Highest risk for severe disease includes the elderly, patients with COPD, and immunocompromised patients |
* Highest risk for severe disease includes the elderly, patients with COPD, and immunocompromised patients |
||
* Immunocompromised patients include solid |
* Immunocompromised patients include solid organ and hematologic transplant patients and those on chemotherapy |
||
** Much higher mortality |
** Much higher mortality |
||
** '''[[Bronchiolitis obliterans syndrome]]''' can be a complication in lung transplant patients with RSV pneumonia |
** '''[[Bronchiolitis obliterans syndrome]]''' can be a complication in lung transplant patients with RSV pneumonia |
||
Line 45: | Line 45: | ||
** Monitor for development of bacterial superinfection |
** Monitor for development of bacterial superinfection |
||
* Hospitalized children may benefit from inhaled [[Is treated by::ribavirin]], though the benefit is unclear |
* Hospitalized children may benefit from inhaled [[Is treated by::ribavirin]], though the benefit is unclear |
||
* In high-risk patients with hematologic malignancies, hematologic transplants, or solid |
* In high-risk patients with hematologic malignancies, hematologic transplants, or solid organ transplants, treat with [[Is treated by::ribavirin]] |
||
* In the highest-risk group of patients, those with allogeneic stem cell transplantation who present with pneumonia, add [[Is treated by::IVIg]] |
* In the highest-risk group of patients, those with allogeneic stem cell transplantation who present with pneumonia, add [[Is treated by::IVIg]] |
||
Line 55: | Line 55: | ||
** Can be considered in patients up to 24 months old if they are still on home oxygen, have had a prolonged hospitalization for severe pulmonary disease or are severely immunocompromised |
** Can be considered in patients up to 24 months old if they are still on home oxygen, have had a prolonged hospitalization for severe pulmonary disease or are severely immunocompromised |
||
[[Category: |
[[Category:Pneumoviridae]] |
Latest revision as of 19:19, 9 January 2023
Background
Microbiology
- Single-stranded, enveloped RNA virus in the Pneumoviridae subfamily of the Paramyxoviridae family
- Two antigenic groups, A and B
Epidemiology
- Worldwide distribution
- In Canada and US, more common in late fall to early spring, but can occur at any time
- Most common cause of bronchiolitis in children
- Spread via droplets, either person-to-person or via fomites
- Typically inoculated into respiratory or ocular mucosa rather than inhaled
- Infection does not generate persistent immunity
Clinical Manifestations
- Incubation period of 3 to 5 days (up to 8 days)
Children
- Generally starts with an upper respiratory tract infection ± fevers and otitis media
- Then can progress to bronchiolitis, pneumonia, tracheobronchitis, and, rarely, croup
- Highest risk for lower respiratory infections are with the first infection, age less than 6 months, and underlying cardiac or lung disease
- Highest risk for requiring hospitalization is premature infants and those with chronic lung disease, congenital heart disease, immunosuppression, and neuromuscular disease
- Wheezing and increased work of breathing are common and cough becomes prominent
- Bronchiolitis may involve inspiratory and expiratory obstruction
- Hypoxia necessitates hospitalization, and may fluctuate, and can also have apnea
Outcomes and Sequelae
- Cough may last for 4 or more weeks, despite resolution of the infection
- Recurrent infections are common
- May have persistent wheezing into adolescence
Adults
- More common in people who work with children and military recruits living in barracks
- Highest risk for severe disease includes the elderly, patients with COPD, and immunocompromised patients
- Immunocompromised patients include solid organ and hematologic transplant patients and those on chemotherapy
- Much higher mortality
- Bronchiolitis obliterans syndrome can be a complication in lung transplant patients with RSV pneumonia
Diagnosis
- Most often with PCR
- Serology not generally helpful
Management
- Supportive care
- Can use puffers and steroids for bronchiolitis with wheezing, but not clear that they are helpful in children
- Monitor for development of bacterial superinfection
- Hospitalized children may benefit from inhaled ribavirin, though the benefit is unclear
- In high-risk patients with hematologic malignancies, hematologic transplants, or solid organ transplants, treat with ribavirin
- In the highest-risk group of patients, those with allogeneic stem cell transplantation who present with pneumonia, add IVIg
Prevention
- Palivizumab is indicated for some high risk groups of infants in order to prevent severe disease1
- Children with hemodynamically significant CHD or CLD if they are <12 months of age at the start of RSV season
- Preterm infants born before 30+0 weeks’ GA who are <6 months of age at the start of RSV season, it is reasonable (but not essential) to offer palivizumab
- Infants in remote communities who would require air transportation for hospitalization born before 36+0 weeks’ GA and <6 months of age at the start of RSV season should be offered palivizumab
- Can be considered in patients up to 24 months old if they are still on home oxygen, have had a prolonged hospitalization for severe pulmonary disease or are severely immunocompromised
References
- ^ Joan L Robinson, Nicole Le Saux. Preventing hospitalizations for respiratory syncytial virus infection. Paediatrics & Child Health. 2015;20(6):321-326. doi:10.1093/pch/20.6.321.