Evidence map›Paper›PMID 31044232›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2020

Use of Routine Complete Blood Count Results to Rule Out Anaplasmosis Without the Need for Specific Diagnostic Testing.

Sarah E Turbett, Melis N Anahtar, Vikram Pattanayak, Marwan M Azar, K C Coffey, George Eng, Joseph W Rudolf, Kent B Lewandrowski, Jason Baron, Eric S Rosenberg and 1 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

11 authors.

Sarah E TurbettDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston.
Melis N AnahtarDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston.
Vikram PattanayakDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston.
Marwan M AzarDepartment of Section of Infectious Diseases, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
K C CoffeyDepartment of Section of Infectious Diseases, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
George EngDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston.
Joseph W RudolfDepartment of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis.
Kent B LewandrowskiDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston.
Jason BaronDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston.
Eric S RosenbergDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston.
John A BrandaDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston.

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
MOLECULAR IMMUNOLOGY AND TUMOR BIOLOGYT32CA009216 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI David Michael Langenau · 1985 to 2026
$10.6M
NCATS NIH HHS UL1 TR001863NCI NIH HHS T32 CA009216
6 · The paper itself

Abstract

backgroundAnaplasmosis presents with fever, headache, and laboratory abnormalities including leukopenia and thrombocytopenia. Polymerase chain reaction (PCR) is the preferred diagnostic but is overutilized. We determined if routine laboratory tests could exclude anaplasmosis, improving PCR utilization.

methodsAnaplasma PCR results from a 3-year period, with associated complete blood count (CBC) and liver function test results, were retrospectively reviewed. PCR rejection criteria, based on white blood cell (WBC) and platelet (PLT) counts, were developed and prospectively applied in a mock stewardship program. If rejection criteria were met, a committee mock-refused PCR unless the patient was clinically unstable or immunocompromised.

resultsWBC and PLT counts were the most actionable routine tests for excluding anaplasmosis. Retrospective review demonstrated that rejection criteria of WBC ≥11 000 cells/µL or PLT ≥300 000 cells/µL would have led to PCR refusal in 428 of 1685 true-negative cases (25%) and 3 of 66 true-positive cases (5%) involving clinically unstable or immunocompromised patients. In the prospective phase, 155 of 663 PCR requests (23%) met rejection criteria and were reviewed by committee, which endorsed refusal in 110 of 155 cases (71%) and approval in 45 (29%), based on clinical criteria. PCR was negative in all 45 committee-approved cases. Only 1 of 110 mock-refused requests yielded a positive PCR result; this patient was already receiving doxycycline at the time of testing.

conclusionsA CBC-based stewardship algorithm would reduce unnecessary Anaplasma PCR testing, without missing active cases. Although the prospectively evaluated screening approach involved medical record review, this was unnecessary to prevent errors and could be replaced by a rejection comment specifying clinical situations that might warrant overriding the algorithm.

Indexed as

Anaplasma phagocytophilumAnaplasmosisAnimalsBlood Cell CountDiagnostic Techniques and ProceduresHumansProspective StudiesRetrospective StudiesAnaplasma phagocytophilumdiagnosisPCRstewardshiputilization management

Identifiers

PMID31044232
PMCPMC7346887

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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.