Evidence map›Paper›PMID 42866625›Full record

ArticleThe journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG2026

The Utility of Using FilmArray Meningitis-Encephalitis PCR Panel (MEP) in Children Admitted With Meningitis and Encephalitis: Is It a Useful Stewardship Tool?

Ban Al-Sayyed, Kelli Covington, Pamela Nicoski, Madeleine Heyn, Gabriella Hunter-McElroy, Shibangi Pal, Marina Feffer, Louise Lie, Jenin Mannaa

Abstract read
In one paragraph

Article in The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Ban Al-SayyedDepartment of Pediatrics, Pediatric Infectious Diseases (BAS), Department of Pharmacy (KC, PN), Strich School of Medicine (MH, GHM, SP); Biostatistics, Clinical Research Office (MF), Infection Prevention at Loyola University Hospital and Medical Center (LL), Maywood, IL.
Kelli CovingtonDepartment of Pediatrics, Pediatric Infectious Diseases (BAS), Department of Pharmacy (KC, PN), Strich School of Medicine (MH, GHM, SP); Biostatistics, Clinical Research Office (MF), Infection Prevention at Loyola University Hospital and Medical Center (LL), Maywood, IL.
Pamela NicoskiDepartment of Pediatrics, Pediatric Infectious Diseases (BAS), Department of Pharmacy (KC, PN), Strich School of Medicine (MH, GHM, SP); Biostatistics, Clinical Research Office (MF), Infection Prevention at Loyola University Hospital and Medical Center (LL), Maywood, IL.
Madeleine HeynDepartment of Pediatrics, Pediatric Infectious Diseases (BAS), Department of Pharmacy (KC, PN), Strich School of Medicine (MH, GHM, SP); Biostatistics, Clinical Research Office (MF), Infection Prevention at Loyola University Hospital and Medical Center (LL), Maywood, IL.
Gabriella Hunter-McElroyDepartment of Pediatrics, Pediatric Infectious Diseases (BAS), Department of Pharmacy (KC, PN), Strich School of Medicine (MH, GHM, SP); Biostatistics, Clinical Research Office (MF), Infection Prevention at Loyola University Hospital and Medical Center (LL), Maywood, IL.
Shibangi PalDepartment of Pediatrics, Pediatric Infectious Diseases (BAS), Department of Pharmacy (KC, PN), Strich School of Medicine (MH, GHM, SP); Biostatistics, Clinical Research Office (MF), Infection Prevention at Loyola University Hospital and Medical Center (LL), Maywood, IL.
Marina FefferDepartment of Pediatrics, Pediatric Infectious Diseases (BAS), Department of Pharmacy (KC, PN), Strich School of Medicine (MH, GHM, SP); Biostatistics, Clinical Research Office (MF), Infection Prevention at Loyola University Hospital and Medical Center (LL), Maywood, IL.
Louise LieDepartment of Pediatrics, Pediatric Infectious Diseases (BAS), Department of Pharmacy (KC, PN), Strich School of Medicine (MH, GHM, SP); Biostatistics, Clinical Research Office (MF), Infection Prevention at Loyola University Hospital and Medical Center (LL), Maywood, IL.
Jenin MannaaSaint Louis University School of Medicine (JM), St. Louis, MO.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveFilmArray Meningitis-Encephalitis Polymerase Chain Reaction (PCR) Panel (MEP) allows for rapid detection or exclusion of pathogens causing meningitis and encephalitis (ME) in neonates and children. Studies showed its high sensitivity and specificity as a tool in diagnosing ME. We conducted a retrospective study in our institution to evaluate MEP usage in our pediatric population, assess the agreement between MEP and cerebrospinal fluid (CSF) culture, and measure the impact of MEP results on discontinuing empiric antimicrobials.

methodsWe reviewed electronic records of patients aged 0 to 18 years admitted with possible ME from January 1, 2019, to April 30, 2023. We excluded patients with ventriculoperitoneal shunt infections, immunocompromised hosts, and patients who did not receive antibiotics.

resultsWe included 136 patients admitted with possible ME and treated with antibiotics. Of all patients, 6.6% had viral PCR detected (n = 9), 3.7% had bacterial PCR detected (n = 5), 89.7% had negative PCR (n = 122). There was high agreement between MEP and CSF culture results (Gwet agreement coefficient was 0.9915). The comparison of MEP vs CSF pleocytosis showed a low sensitivity (24%). Empiric vancomycin was started in 41% of patients who had no additional focus of infection on admission (n = 46/111) and was discontinued within 12 hours of MEP results in 46.6% of cases (n = 21/46). Acyclovir was combined with antibiotics empirically in 13.5% of cases only (n = 15/111).

conclusionMEP is an important diagnostic stewardship tool. It is highly sensitive and specific in diagnosing ME in children. Agreement with CSF cultures is very high. Using CSF pleocytosis as an indication for MEP testing has a low yield.

Indexed as

acyclovirantimicrobial stewardshipCSF cultureCSF pleocytosisdiagnostic toolFilmArray Meningitis-Encephalitismeningo-encephalitisPCR panelvancomycin

Identifiers

PMID42866625
PMCPMC13657059

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.