First and Second Level Haemoglobinopathies Diagnosis: Best Practices of the Italian Society of Thalassemia and Haemoglobinopathies (SITE)
- PMID: 36143073
- PMCID: PMC9501618
- DOI: 10.3390/jcm11185426
First and Second Level Haemoglobinopathies Diagnosis: Best Practices of the Italian Society of Thalassemia and Haemoglobinopathies (SITE)
Abstract
The purpose of this best practice paper is to review the current recommendations for the identification and prenatal diagnosis of hemoglobinopathies.
Methods: The management committee of SITE selected and gathered a multidisciplinary team in order to formulate recommendations based on the available scientific evidence integrated with the opinions of experts, with the purpose of supporting clinicians.
Results: We provide recommendations for first level tests (complete blood count, hemoglobin separation and iron balance), second level tests (molecular diagnosis) and prenatal diagnosis. Five Italian experts in hemoglobinopathies were consulted regarding the orientation of prenatal diagnosis, and for each indication, the degree of agreement among the experts has been specified.
Conclusions: Best practice recommendations are the final outcome of this translational research and allow transfer to daily clinical practice.
Keywords: Thalassemia; diagnostics of hemoglobinopathies; hemoglobinopathies; prenatal diagnosis; sickle cell disease.
Conflict of interest statement
The authors declare no conflict of interest.
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References
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- Schünemann H.J., Wiercioch W., Brozek J., Etxeandia-Ikobaltzeta I., Mustafa R.A., Manja V., Brignardello-Petersen R., Neumann I., Falavigna M., Alhazzani W., et al. GRADE Evidence to Decision (EtD) frameworks for adoption, adaptation, and de novo development of trustworthy recommendations: GRADE-ADOLOPMENT. J. Clin. Epidemiol. 2017;81:101–110. doi: 10.1016/j.jclinepi.2016.09.009. - DOI - PubMed
-
- Traeger-Synodinos J., Harteveld C.L., Old J.M., Petrou M., Galanello R., Giordano P., Angastioniotis M., De la Salle B., Henderson S., May A., et al. EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies. Eur. J. Hum. Genet. 2015;23:426–437. doi: 10.1038/ejhg.2014.131. - DOI - PMC - PubMed
-
- Recommendations for Preconceptional or Antenatal Screening, Prenatal Diagnosis and Genetic Counselling of Haemoglobinopathies. [(accessed on 1 June 2021)]. Available online: http://www.enerca.org.
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