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[Anesthesia and sickle cell disease].

A Guberti, M Marchi, S Tartari

    Minerva Medica
    |November 10, 1984
    PubMed
    Summary
    This summary is machine-generated.

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    Sickle cell anaemia, a common inherited blood disorder, requires careful surgical planning. This study assesses essential pre, per, and post-operative precautions for managing these patients safely.

    Area of Science:

    • Hematology
    • Genetics
    • Medical Science

    Context:

    • Sickle cell anaemia is the most prevalent hereditary haemoglobinopathy.
    • It presents in homozygous or heterozygous forms, sometimes with co-existing haemoglobinopathies.
    • The condition involves complex pathogenesis and physiological imbalances with potentially severe consequences.

    Purpose:

    • To evaluate the critical pre, per, and post-operative precautions for patients with sickle cell anaemia.
    • To provide guidance for optimizing surgical management in this patient population.

    Summary:

    • This work assesses the necessary precautions for surgical procedures in individuals with sickle cell anaemia.
    • It considers the underlying pathophysiology and associated imbalances of the disease.

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  • The evaluation covers the entire perioperative period: before, during, and after surgery.

    • Impact:

    • Ensures improved patient safety and outcomes during surgical interventions.
    • Highlights the importance of specialized care protocols for hereditary haemoglobin disorders.
    • Contributes to the clinical knowledge base for managing sickle cell anaemia patients in surgical settings.