Evidence map›Paper›PMID 30724001›Full record

ArticlePediatric blood & cancer2019

Incidence of invasive Haemophilus influenzae infections in children with sickle cell disease.

Marianne E Yee, Nitya Bakshi, Sara H Graciaa, Peter A Lane, Robert C Jerris, Yun F Wang, Inci Yildirim

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Article in Pediatric blood & cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% of its field
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

4 citing papers in PubMed, 11 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Marianne E YeeDepartment of Pediatrics, Division of Hematology/Oncology, Emory University, Atlanta, Georgia.ORCID 0000-0001-6082-8385
Nitya BakshiDepartment of Pediatrics, Division of Hematology/Oncology, Emory University, Atlanta, Georgia.
Sara H GraciaaAflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia.
Peter A LaneDepartment of Pediatrics, Division of Hematology/Oncology, Emory University, Atlanta, Georgia.
Robert C JerrisDepartment of Pathology and Laboratory Medicine, Children's Healthcare of Atlanta, Atlanta, Georgia.
Yun F WangDepartment of Pathology and Laboratory Medicine, Emory University, Atlanta, Georgia.
Inci YildirimDepartment of Pediatrics, Division of Infectious Diseases, Emory University, Atlanta, Georgia.
Emory University · USAflac (United States) · US

Funding

STUDYING INTRA-INDIVIDUAL PAIN VARIABILITY IN SICKLE CELL DISEASE AND RESOLUTION OF PAIN AFTER HEMATOPOIETIC CELL TRANSPLANT: A NOVEL MODEL SYSTEM TO ELUCIDATE MECHANISMS OF TRANSITION TO CHRONIC PAINK23HL140142 · NHLBI · YALE UNIVERSITY · PI BAKSHI, NITYA · 2018 to 2022
$899k
NHLBI NIH HHS K23 HL140142NIH HHS 1K23HL140142
6 · The paper itself

Abstract

backgroundChildren with sickle cell disease (SCD) are at increased risk for invasive infection with encapsulated bacteria. Antibiotic prophylaxis and immunizations against Streptococcus pneumoniae and Haemophilus influenzae type b (Hib) have decreased the overall incidence of invasive infections and have shifted distribution of serotypes causing disease toward those not covered by immunizations. We sought to determine the current incidence of invasive H. influenzae infections in children with SCD and to describe the clinical features and management of these infections.

methodsMicrobiology reports of a large pediatric tertiary care center were reviewed to identify all isolates of H. influenzae detected in sterile body fluid cultures from January 1, 2010 to December 31, 2017. Results were compared with the center's comprehensive clinical database of all children with SCD to identify all cases of children ages 0 to18 years with SCD with invasive H. influenzae disease for the same time period.

resultsWe captured 2444 patients with SCD, with 14,336 person-years. There were eight episodes of H. influenzae bacteremia in seven children with SCD (five type f, two non-typable, one type a). Most episodes (7 of 8) were in children < 5 years. The incidence rate of invasive H. influenzae in SCD was 0.58/1000 person-years for ages 0 to 18 years and 1.60/1000 person-years for children age < 5 years. There were no deaths from H. influenzae infection.

conclusionsIn the era of universal antibiotic prophylaxis and immunization against Hib, invasive H. influenzae disease due to nonvaccine serotypes remains a risk for children with SCD, particularly those under five years of age.

Indexed as

AdolescentAnemia, Sickle CellChildChild, PreschoolFemaleFollow-Up StudiesGeorgiaHaemophilus InfectionsHaemophilus influenzaeHumansIncidenceInfantInfant, NewbornMalePrognosisbacteremiaHaemophilus influenzaesickle cell disease

Identifiers

PMID30724001
PMCPMC6472970
OpenAlexW2913809307

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Registered trials

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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.