Development of an algorithm for the identification of leukemic hematolymphoid neoplasms in Primary Care patients

Author:

Quirós Covadonga12ORCID,Fonseca Ariana23,Alonso-Álvarez Sara23,Moro-García Marco Antonio2,Alonso-Arias Rebeca24,Morais Lucía-Rita23,Álvarez-Menendez Francisco V.12,Colado Enrique235ORCID

Affiliation:

1. Clinical Biochemistry Department , Hospital Universitario Central de Asturias , Oviedo , Spain

2. Laboratory Medicine Department , Hospital Universitario Central de Asturias , Oviedo , Spain

3. Hematology and Haemotherapy Department , Hospital Universitario Central de Asturias , Oviedo , Spain

4. Immunology Department , Hospital Universitario Central de Asturias , Oviedo , Spain

5. Laboratory Medicine Department, Hospital Universitario Central de Asturias, Avda. Roma s/n – 33011 Oviedo, Spain; Hematology and Haemotherapy Department, Hospital Universitario Central de Asturias, Avda. Roma s/n – 33011 Oviedo, Spain; and Hematology and Haemotherapy Department, Laboratory of Medicine , Hospital Universitario Central de Asturias , Oviedo , Spain , Phone: +34 985 10 80 00, Ext 37138

Abstract

Abstract Background Diagnosis of hematolymphoid neoplasm (HLN) requires different technologies which are performed on a patient basis instead of per protocol. We hypothesize that integration of hematimetric and cytological analysis along with multiparametric flow cytometry (MFC) provides a framework to evaluate peripheral blood (PB) samples from Primary Care. Methods Samples from patients with persistent (>3 months) lymphocytosis (>5 × 109/L) and/or monocytosis (>109/L) or the presence of atypical and/or blast cells upon the smear review were analyzed by MFC concurrent to cytological analysis. MFC studies were carried out following standardized procedures. Results In a 3-year period, smear review and MFC were performed simultaneously in 350 samples, demonstrating HLN in 194 cases (55.4%). In 156 cases, reactive cell populations were found. The combination of age, absolute lymphocyte count (ALC), hemoglobin and platelets provided the best correlation with MFC for the presence of a chronic lymphoproliferative disorder (CLPD) in lymphocytosis [area under the curve (AUC) 0.891, p < 0.05]. A model evaluating the probability of CLPD has been proposed and validated in an independent cohort. Conclusions A strategy to perform MFC studies following standardized procedures has proven to be useful to evaluate samples from patients in Primary Care centers for HLN diagnosis or reactive conditions, providing a sensitive and rapid clinical orientation and avoiding unnecessary consultations in routine clinical practice. The probability for the presence of CLPD in PB can be calculated and help guide decision-making regarding further testing.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,Public Health, Environmental and Occupational Health,Health Policy,Medicine (miscellaneous)

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