Impact of optimizing pre-analytical phase on the diagnosis of gestational diabetes and related outcomes

Author:

Szoke Dominika1,Borille Simona1,Cardellicchio Manuela2,Spadaccini Giovanna3,Taricco Emanuela4,Vignali Michele35,Cetin Irene246,Birindelli Sarah1,Panteghini Mauro16

Affiliation:

1. UOC Patologia Clinica , Milan , Italy

2. UOC Ostetricia e Ginecologia Presidio Luigi Sacco , Milan , Italy

3. UOC Ostetricia e Ginecologia Presidio Macedonio Melloni , Milan , Italy

4. UOC Ostetricia e Ginecologia Presidio Vittore Buzzi, ASST Fatebenefratelli-Sacco , Milan , Italy

5. Dipartimento di Scienze Biomediche per la Salute , Milan , Italy

6. Dipartimento di Scienze Biomediche e Cliniche “Luigi Sacco” , Università degli Studi , Milan , Italy

Abstract

Abstract Objectives Pre-analytical plasma glucose (PG) sampling methodology may significantly affect gestational diabetes mellitus (GDM) incidence, but no studies directly examined the impact on perinatal outcomes. We compared the effect on oral glucose tolerance test (OGTT) results of using for blood sampling the traditional sodium fluoride (NaF) tubes, batched at controlled temperature, and the more effective citrate-buffered tubes, in terms of GDM diagnosis and related outcomes. Methods We evaluated 578 pregnant women performing OGTT between 24- and 28-weeks’ gestation. Paired NaF and citrate blood samples were drawn and analyzed for PG. GDM diagnosis was made by applying the ‘one-step’ American Diabetes Association strategy. Data on perinatal outcomes were collected in a subset of 330 women who delivered in our hospital network. Results Using the standard NaF approach, 69 (11.9%) GDM women were detected. Using citrate PG values, 90 women were additionally identified as GDM, increasing the GDM prevalence to 27.5%. Perinatal outcomes were analyzed according to the different diagnostic allocation (NaF-diagnosed GDM, additional citrate-diagnosed GDM, and no GDM). NaF-diagnosed GDM showed a higher incidence of large for gestational age (LGA) (p=0.034), and of cesarean and preterm delivery (p<0.01) vs. no GDM. The only outcome remaining more frequent in the additional citrate diagnosed GDM when compared with no GDM group was LGA (17.2 vs. 6.8%, p=0.025). Conclusions If a health care system plans to use citrate tubes for GDM diagnosis, considerations about clinical implications are mandatory by balancing higher sensitivity in detecting a poor glycemic control with effects on outcomes to avoid “overdiagnosis”.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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