Process Control in Immunohematology

Process Control in Immunohematology

Immunohematology

Fundamental in medical procedures, Immunohematology evolves continuously, requiring updates from professionals and controls for more assertive and efficient results

Immunohematology is a specialty of Hemotherapy related to transfusion medicine. The analyzes of this specialty, in addition to being fundamental for the diagnosis of pathologies of the hematological system, avoid transfusion reactions.

As with any medical or technical procedure, the main objective of transfusion is to bring benefits to the recipient, despite the risks involved. In this sense, immunohematological tests mitigate these risks, performing the verification of blood compatibility between donor and recipient, in order to ensure therapeutic efficacy and safety of the donation.

Immunohematology is part of a scenario of continuous evolution, from the quality control of reagents and techniques, to the insertion of new automated systems, in addition to professional specialization.

Applied to diagnosis, this evolutionary scenario of the exam impacts on improvements and, consequently, more assertive and efficient results. Additionally, it contributes to better performance for the professionals involved.

In the last ten years, new analytical methods for the production of monoclonal antibodies have revolutionized the diagnosis of immunohematological analysis. According to studies performed, for the polymorphism of human red blood cells, the production of new inputs becomes essential. Biotechnology has contributed significantly to the specialty, adding more sensitivity to the studies of various methods and equipment.

Control of processes and deviations from results

The main challenge of Immunohematology is professional training to identify and improve the critical points of the processes, such as: collection errors, failures in the correlation of results with the clinical picture and in the specification of quality control. The technical analysis team must always be updated, whether in the literature, in the technical practice of new and reactive systems and in the interpretation of all process variants.

In order to establish safe and reliable processes in Immunohematology exams, some factors are fundamental, such as: quality control, professional training and clinical knowledge, which collaborate in the correlation of results with the patient’s clinical condition.

 Quality Control

Routine transfusion and immunohematology studies of patients include several tests to ensure safe and effective transfusions. Controlling the quality of the reagents, monitoring the efficiency of the analyzes and other techniques involved in the diagnosis, evidences the commitment to the excellence of the exams. Applying continuous improvement increases productivity, reduces rework, waste and process inefficiency.

Professional updating and knowledge added to the frequent use of quality control is one of the main factors in eliminating errors. Keeping all variables under control, from sample collection to the final result, including equipment and reagents, will give credibility to the report and security to the analysis routine.

Considering the potential severity of some transfusion reactions, it is essential to adopt measures to avoid fatal occurrences. In this sense, implementing preventive actions in the routine that allow the early identification of failures guarantees the release of accurate results and allows the immediate establishment of appropriate therapeutic measures for the patient.

The Quality Control (QC) for Immunohematology offered by Controllab has a range of programs and tests to ensure the reliability of manual and automated analysis processes.

Check the Immunohematology programs that Controllab offers:

Programs

Available Tests

Available Services

General
  • ABO and Rhesus Rh Systems

  • Extravascular Antibodies Test - PAI (Indirect Coombs)

Proficiency TestingInternal Control
Automation
  • ABO and Rhesus System – Rh (D)

  • Extravascular Antibody Test – PAI (Indirect Coombs)

  • Intravascular Antibodies Test – TAD (Direct Coombs)

Proficiency TestingInternal Control
Eluate
  • Direct Coombs Conclusion

  • Eluate

  • IAI Identification

Proficiency TestingInternal Control
Fenotipagem Rh e Kell
  • D, C, c, E, e, Cw, K, k, Kpa, Kpb antigens

  • Rh system genotypes

Proficiency Testing
IAI
  • Irregular Antibodies Identification - IAI

Proficiency TestingInternal Control
Cross-matching
  • Cross-matching

  • ABO System and Rhesus System – Rh

Proficiency Testing
TAD
  • Intravascular antibodies Test – TAD (Direct Coombs)

Proficiency Testing
Anti-A Titration
  • Anti-A Titration

Proficiency Testing
Anti-B Titration
  • Anti-B Titration

Proficiency Testing
Anti-D Titration
  • Anti-D Titration

Proficiency Testing

Related program

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Certified Reference Material Producer

Accredited by Coordenação-Geral de Acreditação do Inmetro

Controllab has been accredited as a Certified Reference Material (CRM) Producer since 2016 by Cgcre, under number PMR 0009. The conformity assessment is carried out in accordance with the requirements established in ABNT NBR ISO 17034 and Inmetro standards, ensuring competence for the production of CRMs, as defined in the Scope of Accreditation.

This accreditation attests to Controllab’s technical competence in producing CRMs according to international requirements and enables it to be recognized in other countries, under mutual recognition agreements, thereby reducing technical barriers between Brazil and other countries across continents.

Materiais de Referência Certificados - PMR 0009 - ABNT NBR ISO 17034-Controllab
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Calibration Laboratory

Accredited by Coordenação-Geral de Acreditação do Inmetro

In December 2002, the Calibration Laboratory was accredited by Cgcre. With this recognition, it became part of the Brazilian network of accredited laboratories, under number 214. Since then, it has been periodically evaluated for the maintenance and/or extension of its accreditation.

The Inmetro seal attests to Controllab’s technical competence, credibility, and operational capability for calibration services, in accordance with the requirements of ABNT NBR ISO/IEC 17025.

Calibração de Instrumentos - CAL 0214 - ABNT NBR ISO/IEC 17025 - Controllab
Cgcre is signatory to the Mutual Recognition Arrangements of the International Laboratory Accreditation Cooperation (ILAC) and Interamerican Accreditation Cooperation (IAAC).

PEP 0003

Proficiency Test Provider

Accredited by Coordenação-Geral de Acreditação do Inmetro

In September 2011, Controllab was accredited by Cgcre as a proficiency test provider, under nº PEP0003. Initially as part of a pilot project by Inmetro, this accreditation was based on ILAC G13: 2007 and included several clinical and hemotherapy tests. In the periodic evaluations of this accreditation, new segments and tests are included and the evaluation is now conducted according to ABNT NBR ISO/IEC 17043.

This accreditation attests to Controllab’s technical competence to develop and conduct proficiency tests in accordance with international requirements and enables it to be recognized in other countries, in accordance with mutual recognition agreements signed by Brazil in Mercosur, the Americas and Europe.

PEP 0003 - ABNT NBR ISO-IEC 17043 - Controllab

Cgcre is signatory to the Mutual Recognition Arrangements of the International Laboratory Accreditation Cooperation (ILAC) and Interamerican Accreditation Cooperation (IAAC).