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Reply to: “Considerations about the use of glucometers for testing glucose tolerance”

  • Estéfani Martínez-Chávez ORCID logo , Blanca Fabre-Estremera , Marta Manzano Ocaña , Pilar Fernández-Calle , Antonio Buño Soto und Paloma Oliver EMAIL logo
Veröffentlicht/Copyright: 2. Dezember 2024

To the Editor,

We thank Lavin-Gomez B.A. and Guerra Ruíz A.R. [1] for their valuable comments to our paper titled “Use of point-of-care glucometers during an oral glucose tolerance test in children for prediabetes and diabetes diagnosis: A comparison study” [2]. We are extremely grateful for your interest in our study and for your suggestions, which substantially contribute to the debate on this issue. Please, find below our response to your considerations.

  1. Pre-analytical sample handling: Thank you for your observation. We would like to clarify that serum tubes with gel are used in our center during the oral glucose tolerance test. A centrifuge is available in the Unit of Diabetes to minimize the effects of in vitro glycolysis. In our paper, we acknowledge the potential influence of in vitro glycolysis on fasting samples as a limitation. Thanks to the study, our sample handling protocol was optimized to ensure that fasting samples are centrifuged within 20 min of collection.

  2. Correlation between glucose measurements: Comparative analysis of the methods revealed that the differences observed in glucose results obtained with the POCTACI (Accu-Chek® Inform-II, Roche Diagnostics, Basel, Switzerland) and the central laboratory (Atellica®Solution-CH; Siemens Healthineers, Erlangen, Germany) were not statistically significant. These differences complied with our quality specifications for glucose concentrations of 100, 125, 140 and 200 mg/dL. However, in the light of the clinical impact of diagnostic discrepancies, we decided to examine the diagnostic concordance between the two methods.

    The results revealed that differences in glucose concentrations between POCTACI and the central laboratory tended to increase as glucose concentrations rose. Thus, the POCT glucometer yielded lower results than the central laboratory at higher glucose concentrations. Due to the study design, the reason for lower glucometer results at 30, 60 and 120 min, as compared to laboratory results, could not be determined. Future research that controls for additional variables may help explain these observed differences.

  3. Interference of hematocrit in glucose measurement: The POCTACI and POCTACP glucometers (Accu-Chek® Performa, Roche Diagnostics, Basel, Switzerland) used in our laboratory do not measure hematocrit. Given the interest in this variable, we examined hematocrit results in our study population. Of the 98 patients included, a hemogram was included in the laboratory test request of 50 patients. POCTACI and laboratory-based diagnoses were consistent in 68 % (34) of cases (see Figure 1).

    Separate analysis of diagnostic discrepancies revealed that in 3 of the 4 patients with hematocrit results >43 % (range 44–49 %), diagnostic discrepancies could have had a clinical impact. In all cases, the results obtained with the glucometer were lower than those of the central laboratory. Additionally, in 2 of the 5 cases with hematocrit results <43 % (range 36–42 %), diagnostic discrepancies could have had clinical implications. In the both cases, lower results were obtained with the glucometer, as compared to the laboratory (see Table 1). Therefore, in our study, when hematocrit was <43 %, the inverse relationship between hematocrit and glucose described in the literature [3] was not observed.

    In our study population, we found that glucometer tended to underdiagnose prediabetes and diabetes, except in cases of impaired fasting glycemia. Thus, diagnostic discrepancies in the latter were probably due to in vitro glycolysis in fasting samples. In our study, a clear influence of hematocrit was not observed on glucose results.

Next-generation glucometers with capacity to measure hematocrit could yield more precise readings and reduce variations. This would pave the way for the potential use of POCT glucometers for diagnostic purposes in the near future. We once again thank Lavin-Gomez BA and Guerra Ruíz AR for their valuable comments, which contributed to the debate about the use of glucometers in the clinic.

Figure 1: 
Diagnostic concordance between POCTACI and the central laboratory as a function of hematocrit values. Distribution of the 50 patients with hematocrit values available. Analysis of diagnostic concordance between POCTACI and the central laboratory. Hematocrit values were categorized into three groups: hematocrit<43 % (mean 41 %, SD: 1.8, diagnostic concordance 73 %); hematocrit=43 % (diagnostic concordance 60 %) and hematocrit>43 % (mean 46 %, SD: 1.5, with a diagnostic concordance of 63 %).
Figure 1:

Diagnostic concordance between POCTACI and the central laboratory as a function of hematocrit values. Distribution of the 50 patients with hematocrit values available. Analysis of diagnostic concordance between POCTACI and the central laboratory. Hematocrit values were categorized into three groups: hematocrit<43 % (mean 41 %, SD: 1.8, diagnostic concordance 73 %); hematocrit=43 % (diagnostic concordance 60 %) and hematocrit>43 % (mean 46 %, SD: 1.5, with a diagnostic concordance of 63 %).

Table 1:

Diagnostic discordance between POCTACI and the central laboratory.

POCTACI Central laboratory Clinical impact Hematocrit, %
IFG Normal None 36
IFG Normal 40
IFG Normal 42
IFG Normal 43
IFG Normal ?
IFG Normal ?
IFG Normal ?
Normal IGT 47
IFG IFG+IGT ?
IGT Diabetes ?
Normal IGT Mild 41
IGT Diabetes 44
IGT Diabetes ?
Normal IGT Severe 48
Normal IGT ?
IFG+IGT Diabetes 47
IGT Diabetes 41
  1. IFG, impaired fasting glucose; IGT, impaired glucose tolerance; POCTACI, connected glucometer.


Corresponding author: Paloma Oliver, Department of Laboratory Medicine, La Paz University Hospital, Paseo de la Castellana 261, Madrid 28046, Spain, E-mail:

  1. Research ethics: Not applicable.

  2. Informed consent: Not applicable.

  3. Author contributions: Martínez Chávez E: writing – original draft, writing – review and editing, visualization. Fabre-Estremera B, Manzano Ocaña M, Fernández-Calle P, Buño Soto A and Oliver P: writing – review and editing. All authors have accepted responsibility for the entire content of this manuscript and have approved its submission.

  4. Use of Large Language Models, AI and Machine Learning Tools: None declared.

  5. Conflict of interest: The authors state no conflict of interest.

  6. Research funding: None declared.

  7. Data availability: Not applicable.

  8. Article Note: The original article can be found here: https://doi.org/10.1515/almed-2024-0148.

References

1. Lavin-Gomez, BA, Guerra Ruíz, AR. Consideraciones acerca del uso de glucómetros durante la prueba de tolerancia oral a la glucosa [Manuscrito no publicado]. Servicio de Análisis Clínicos, Hospital Universitario Marqués de Valdecilla.Suche in Google Scholar

2. Fabre-Estremera, B, Martínez-Chávez, E, Manzano Ocaña, M, Carcavilla Urquí, A, Morales Sánchez, MÁ, Pinilla Tejado, I, et al.. Use of point-of-care glucometers during an oral glucose tolerance test in children for prediabetes and diabetes diagnosis: a comparison study. Estudio comparativo. Adv Lab Med 2024;5:197–204. https://doi.org/10.1515/almed-2024-0017.Suche in Google Scholar PubMed PubMed Central

3. Solnica, B, Skupien, J, Kusnierz-Cabala, B, Slowinska-Solnica, K, Witek, P, Cempa, A, et al.. The effect of hematocrit on the results of measurements using glucose meters based on different techniques. Clin Chem Lab Med 2011;50:361–5. https://doi.org/10.1515/cclm.2011.770.Suche in Google Scholar

Received: 2024-10-08
Accepted: 2024-10-13
Published Online: 2024-12-02

© 2024 the author(s), published by De Gruyter, Berlin/Boston

This work is licensed under the Creative Commons Attribution 4.0 International License.

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  29. Respuesta a la carta al editor: “Consideraciones acerca del uso de glucómetros durante la prueba de tolerancia oral a la glucosa” (https://doi.org/10.1515/almed-2024-0108)
Heruntergeladen am 24.9.2025 von https://www.degruyterbrill.com/document/doi/10.1515/almed-2024-0169/html
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