Next-generation reference intervals for pediatric hematology

Standard

Next-generation reference intervals for pediatric hematology. / Zierk, Jakob; Hirschmann, Johannes; Toddenroth, Dennis; Arzideh, Farhad; Haeckel, Rainer; Bertram, Alexander; Cario, Holger; Frühwald, Michael C; Groß, Hans-Jürgen; Groening, Arndt; Grützner, Stefanie; Gscheidmeier, Thomas; Hoff, Torsten; Hoffmann, Reinhard; Klauke, Rainer; Krebs, Alexander; Lichtinghagen, Ralf; Mühlenbrock-Lenter, Sabine; Neumann, Michael; Nöllke, Peter; Niemeyer, Charlotte M; Razum, Oliver; Ruf, Hans-Georg; Steigerwald, Udo; Streichert, Thomas; Torge, Antje; Rascher, Wolfgang; Prokosch, Hans-Ulrich; Rauh, Manfred; Metzler, Markus.

In: CLIN CHEM LAB MED, Vol. 57, No. 10, 25.09.2019, p. 1595-1607.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Zierk, J, Hirschmann, J, Toddenroth, D, Arzideh, F, Haeckel, R, Bertram, A, Cario, H, Frühwald, MC, Groß, H-J, Groening, A, Grützner, S, Gscheidmeier, T, Hoff, T, Hoffmann, R, Klauke, R, Krebs, A, Lichtinghagen, R, Mühlenbrock-Lenter, S, Neumann, M, Nöllke, P, Niemeyer, CM, Razum, O, Ruf, H-G, Steigerwald, U, Streichert, T, Torge, A, Rascher, W, Prokosch, H-U, Rauh, M & Metzler, M 2019, 'Next-generation reference intervals for pediatric hematology', CLIN CHEM LAB MED, vol. 57, no. 10, pp. 1595-1607. https://doi.org/10.1515/cclm-2018-1236

APA

Zierk, J., Hirschmann, J., Toddenroth, D., Arzideh, F., Haeckel, R., Bertram, A., Cario, H., Frühwald, M. C., Groß, H-J., Groening, A., Grützner, S., Gscheidmeier, T., Hoff, T., Hoffmann, R., Klauke, R., Krebs, A., Lichtinghagen, R., Mühlenbrock-Lenter, S., Neumann, M., ... Metzler, M. (2019). Next-generation reference intervals for pediatric hematology. CLIN CHEM LAB MED, 57(10), 1595-1607. https://doi.org/10.1515/cclm-2018-1236

Vancouver

Zierk J, Hirschmann J, Toddenroth D, Arzideh F, Haeckel R, Bertram A et al. Next-generation reference intervals for pediatric hematology. CLIN CHEM LAB MED. 2019 Sep 25;57(10):1595-1607. https://doi.org/10.1515/cclm-2018-1236

Bibtex

@article{74ff300c0e2844499ece53746ab6e38e,
title = "Next-generation reference intervals for pediatric hematology",
abstract = "Background Interpreting hematology analytes in children is challenging due to the extensive changes in hematopoiesis that accompany physiological development and lead to pronounced sex- and age-specific dynamics. Continuous percentile charts from birth to adulthood allow accurate consideration of these dynamics. However, the ethical and practical challenges unique to pediatric reference intervals have restricted the creation of such percentile charts, and limitations in current approaches to laboratory test result displays restrict their use when guiding clinical decisions. Methods We employed an improved data-driven approach to create percentile charts from laboratory data collected during patient care in 10 German centers (9,576,910 samples from 358,292 patients, 412,905-1,278,987 samples per analyte). We demonstrate visualization of hematology test results using percentile charts and z-scores (www.pedref.org/hematology) and assess the potential of percentiles and z-scores to support diagnosis of different hematological diseases. Results We created percentile charts for hemoglobin, hematocrit, red cell indices, red cell count, red cell distribution width, white cell count and platelet count in girls and boys from birth to 18 years of age. Comparison of pediatricians evaluating complex clinical scenarios using percentile charts versus conventional/tabular representations shows that percentile charts can enhance physician assessment in selected example cases. Age-specific percentiles and z-scores, compared with absolute test results, improve the identification of children with blood count abnormalities and the discrimination between different hematological diseases. Conclusions The provided reference intervals enable precise assessment of pediatric hematology test results. Representation of test results using percentiles and z-scores facilitates their interpretation and demonstrates the potential of digital approaches to improve clinical decision-making.",
author = "Jakob Zierk and Johannes Hirschmann and Dennis Toddenroth and Farhad Arzideh and Rainer Haeckel and Alexander Bertram and Holger Cario and Fr{\"u}hwald, {Michael C} and Hans-J{\"u}rgen Gro{\ss} and Arndt Groening and Stefanie Gr{\"u}tzner and Thomas Gscheidmeier and Torsten Hoff and Reinhard Hoffmann and Rainer Klauke and Alexander Krebs and Ralf Lichtinghagen and Sabine M{\"u}hlenbrock-Lenter and Michael Neumann and Peter N{\"o}llke and Niemeyer, {Charlotte M} and Oliver Razum and Hans-Georg Ruf and Udo Steigerwald and Thomas Streichert and Antje Torge and Wolfgang Rascher and Hans-Ulrich Prokosch and Manfred Rauh and Markus Metzler",
year = "2019",
month = sep,
day = "25",
doi = "10.1515/cclm-2018-1236",
language = "English",
volume = "57",
pages = "1595--1607",
journal = "CLIN CHEM LAB MED",
issn = "1434-6621",
publisher = "Walter de Gruyter GmbH & Co. KG",
number = "10",

}

RIS

TY - JOUR

T1 - Next-generation reference intervals for pediatric hematology

AU - Zierk, Jakob

AU - Hirschmann, Johannes

AU - Toddenroth, Dennis

AU - Arzideh, Farhad

AU - Haeckel, Rainer

AU - Bertram, Alexander

AU - Cario, Holger

AU - Frühwald, Michael C

AU - Groß, Hans-Jürgen

AU - Groening, Arndt

AU - Grützner, Stefanie

AU - Gscheidmeier, Thomas

AU - Hoff, Torsten

AU - Hoffmann, Reinhard

AU - Klauke, Rainer

AU - Krebs, Alexander

AU - Lichtinghagen, Ralf

AU - Mühlenbrock-Lenter, Sabine

AU - Neumann, Michael

AU - Nöllke, Peter

AU - Niemeyer, Charlotte M

AU - Razum, Oliver

AU - Ruf, Hans-Georg

AU - Steigerwald, Udo

AU - Streichert, Thomas

AU - Torge, Antje

AU - Rascher, Wolfgang

AU - Prokosch, Hans-Ulrich

AU - Rauh, Manfred

AU - Metzler, Markus

PY - 2019/9/25

Y1 - 2019/9/25

N2 - Background Interpreting hematology analytes in children is challenging due to the extensive changes in hematopoiesis that accompany physiological development and lead to pronounced sex- and age-specific dynamics. Continuous percentile charts from birth to adulthood allow accurate consideration of these dynamics. However, the ethical and practical challenges unique to pediatric reference intervals have restricted the creation of such percentile charts, and limitations in current approaches to laboratory test result displays restrict their use when guiding clinical decisions. Methods We employed an improved data-driven approach to create percentile charts from laboratory data collected during patient care in 10 German centers (9,576,910 samples from 358,292 patients, 412,905-1,278,987 samples per analyte). We demonstrate visualization of hematology test results using percentile charts and z-scores (www.pedref.org/hematology) and assess the potential of percentiles and z-scores to support diagnosis of different hematological diseases. Results We created percentile charts for hemoglobin, hematocrit, red cell indices, red cell count, red cell distribution width, white cell count and platelet count in girls and boys from birth to 18 years of age. Comparison of pediatricians evaluating complex clinical scenarios using percentile charts versus conventional/tabular representations shows that percentile charts can enhance physician assessment in selected example cases. Age-specific percentiles and z-scores, compared with absolute test results, improve the identification of children with blood count abnormalities and the discrimination between different hematological diseases. Conclusions The provided reference intervals enable precise assessment of pediatric hematology test results. Representation of test results using percentiles and z-scores facilitates their interpretation and demonstrates the potential of digital approaches to improve clinical decision-making.

AB - Background Interpreting hematology analytes in children is challenging due to the extensive changes in hematopoiesis that accompany physiological development and lead to pronounced sex- and age-specific dynamics. Continuous percentile charts from birth to adulthood allow accurate consideration of these dynamics. However, the ethical and practical challenges unique to pediatric reference intervals have restricted the creation of such percentile charts, and limitations in current approaches to laboratory test result displays restrict their use when guiding clinical decisions. Methods We employed an improved data-driven approach to create percentile charts from laboratory data collected during patient care in 10 German centers (9,576,910 samples from 358,292 patients, 412,905-1,278,987 samples per analyte). We demonstrate visualization of hematology test results using percentile charts and z-scores (www.pedref.org/hematology) and assess the potential of percentiles and z-scores to support diagnosis of different hematological diseases. Results We created percentile charts for hemoglobin, hematocrit, red cell indices, red cell count, red cell distribution width, white cell count and platelet count in girls and boys from birth to 18 years of age. Comparison of pediatricians evaluating complex clinical scenarios using percentile charts versus conventional/tabular representations shows that percentile charts can enhance physician assessment in selected example cases. Age-specific percentiles and z-scores, compared with absolute test results, improve the identification of children with blood count abnormalities and the discrimination between different hematological diseases. Conclusions The provided reference intervals enable precise assessment of pediatric hematology test results. Representation of test results using percentiles and z-scores facilitates their interpretation and demonstrates the potential of digital approaches to improve clinical decision-making.

U2 - 10.1515/cclm-2018-1236

DO - 10.1515/cclm-2018-1236

M3 - SCORING: Journal article

C2 - 31005947

VL - 57

SP - 1595

EP - 1607

JO - CLIN CHEM LAB MED

JF - CLIN CHEM LAB MED

SN - 1434-6621

IS - 10

ER -