Monitoring

Patients with mild hemophilia A or B should have a comprehensive evaluation once a year at their hemophilia treatment center. Patients with moderate or severe hemophilia A or B should have their comprehensive evaluation every 6 months. Patients are evaluated by a team of health professionals with expertise in hemophilia, including:

  • Physicians

  • Clinical and research nurses

  • Physical therapists

  • Dentists

  • Social workers

  • Geneticists.

Referral to other health professionals, including orthopedic specialists, the pain team, hepatology specialists, and infectious disease specialists, is recommended on an individual basis to manage any chronic complications.

Assessment by a physical therapist should be included in the comprehensive evaluation to identify and assess musculoskeletal problems, and discuss physical therapy and rehabilitation needs.[78]

Standard laboratory testing includes complete blood count, factor VIII or factor IX inhibitor screen, hepatitis, and HIV screening. For those patients with hepatitis C (HCV), testing should also include liver function tests, prothrombin time, HCV-viral load, and alpha-fetoprotein. For those patients with HIV, testing should also include HIV-viral load and CD4 count.

In patients with hemophilia receiving emicizumab prophylaxis, factor VIII assay and factor VIII inhibitor Bethesda assay should be by the chromogenic methods using bovine reagents.[38][61]

Factor replacement therapy, by measurement of blood factor levels (primarily in inpatients), is usually done by measuring a trough level just before the first morning dose. Adjustments to the dose and frequency of dosing are made accordingly.

Screening for the development of inhibitory antibodies

Patients with inhibitors also need specific monitoring. The World Federation of Hemophilia guidelines state that indications for inhibitor screening include:[38]

  • Initial factor exposure

  • Intensive factor exposure (e.g., daily exposure for more than 5 days)

  • Recurrent bleeds or target joint bleeds (despite adequate clotting factor concentrate replacement therapy)

  • Failure to respond to adequate clotting factor concentrate replacement therapy

  • Lower than expected factor recovery or half-­life after clotting factor concentrate replacement therapy

  • Suboptimal clinical or laboratory response to clotting factor concentrate replacement therapy

  • Before surgery

  • Suboptimal postoperative response to clotting factor concentrate replacement therapy.

Patients with mild hemophilia who are infrequently infused may be checked every 12 months. If patients with inhibitors have an acute bleed, treatment is complex and should be managed in a specialist center.

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