Evaluation and Medical Management of the Pediatric Patient With Orbital Cellulitis/Abscess: A Systematic Review.


Journal

Journal of hospital medicine
ISSN: 1553-5606
Titre abrégé: J Hosp Med
Pays: United States
ID NLM: 101271025

Informations de publication

Date de publication:
11 2021
Historique:
received: 13 05 2021
accepted: 02 09 2021
pubmed: 4 11 2021
medline: 15 12 2021
entrez: 3 11 2021
Statut: ppublish

Résumé

Pediatric orbital cellulitis/abscess (OCA) can lead to vision loss, intracranial extension of infection, or cavernous thrombosis if not treated promptly. No widely recognized guidelines exist for the medical management of OCA. The objective of this review was to summarize existing evidence regarding the role of inflammatory markers in distinguishing disease severity and need for surgery; the role of imaging in OCA evaluation; and the microbiology of OCA over the past 2 decades. This review was reported in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Searches were performed in MEDLINE (Ovid), Web of Science Core Collection, Scopus, CINAHL (EBSCO), and Cochrane Central Register of Controlled Trials (CENTRAL), most recently on February 9, 2021. A total of 63 studies were included. Most were descriptive and assessed to have poor quality with high risk of bias. The existing publications evaluating inflammatory markers in the diagnosis of OCA have inconsistent results. Computed tomography imaging remains the modality of choice for evaluating orbital infection. The most common organisms recovered from intraoperative cultures are Streptococcus species (Streptococcus anginosus group, group A Streptococcus, and pneumococcus) and Staphylococcus aureus. Methicillin-resistant S aureus in culture-positive cases had a median prevalence of 3% (interquartile range, 0%-13%). This systematic review summarizes existing literature concerning inflammatory markers, imaging, and microbiology for OCA evaluation and management. High-quality evidence is still needed to define the optimal medical management of OCA.

Sections du résumé

BACKGROUND AND OBJECTIVES
Pediatric orbital cellulitis/abscess (OCA) can lead to vision loss, intracranial extension of infection, or cavernous thrombosis if not treated promptly. No widely recognized guidelines exist for the medical management of OCA. The objective of this review was to summarize existing evidence regarding the role of inflammatory markers in distinguishing disease severity and need for surgery; the role of imaging in OCA evaluation; and the microbiology of OCA over the past 2 decades.
METHODS
This review was reported in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Searches were performed in MEDLINE (Ovid), Web of Science Core Collection, Scopus, CINAHL (EBSCO), and Cochrane Central Register of Controlled Trials (CENTRAL), most recently on February 9, 2021.
RESULTS
A total of 63 studies were included. Most were descriptive and assessed to have poor quality with high risk of bias. The existing publications evaluating inflammatory markers in the diagnosis of OCA have inconsistent results. Computed tomography imaging remains the modality of choice for evaluating orbital infection. The most common organisms recovered from intraoperative cultures are Streptococcus species (Streptococcus anginosus group, group A Streptococcus, and pneumococcus) and Staphylococcus aureus. Methicillin-resistant S aureus in culture-positive cases had a median prevalence of 3% (interquartile range, 0%-13%).
CONCLUSION
This systematic review summarizes existing literature concerning inflammatory markers, imaging, and microbiology for OCA evaluation and management. High-quality evidence is still needed to define the optimal medical management of OCA.

Identifiants

pubmed: 34730499
pii: jhm.3707
doi: 10.12788/jhm.3707
doi:

Types de publication

Journal Article Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

680-687

Auteurs

Alina G Burek (AG)

Children's Wisconsin, Milwaukee, Wisconsin.
Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin.

Svetlana Melamed (S)

Children's Wisconsin, Milwaukee, Wisconsin.
Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin.

Tracey Liljestrom (T)

Children's Wisconsin, Milwaukee, Wisconsin.
Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin.

Jing Qi (J)

Children's Wisconsin, Milwaukee, Wisconsin.
Department of Radiology, Medical College of Wisconsin, Milwaukee, Wisconsin.

Teresa G Kelly (TG)

Children's Wisconsin, Milwaukee, Wisconsin.
Department of Radiology, Medical College of Wisconsin, Milwaukee, Wisconsin.

Elizabeth Suelzer (E)

MCW Libraries, Medical College of Wisconsin, Milwaukee, Wisconsin.

Michelle Mitchell (M)

Children's Wisconsin, Milwaukee, Wisconsin.
Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin.

Gerald J Harris (GJ)

Children's Wisconsin, Milwaukee, Wisconsin.
Department of Ophthalmology and Visual Sciences, Medical College of Wisconsin, Milwaukee, Wisconsin.

Peter L Havens (PL)

Children's Wisconsin, Milwaukee, Wisconsin.
Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin.

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Classifications MeSH