What needs to be monitored in patients on infliximab (chimeric monoclonal antibody against tumor necrosis factor-alpha (TNF-alpha))?

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Last updated: October 23, 2025View editorial policy

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Monitoring Requirements for Patients on Infliximab

Patients on infliximab require regular monitoring for tuberculosis, platelet counts, infections, and clinical response, with particular attention to tuberculosis screening before and during treatment. 1

Tuberculosis Monitoring

  • Before starting infliximab, all patients should undergo tuberculosis screening including clinical history, physical examination, chest radiograph, and tuberculin skin testing (if not on immunosuppressive therapy) 1
  • Patients with abnormal chest radiographs or history of TB should be referred to a specialist with expertise in TB management 1
  • Clinical awareness of TB should be maintained throughout anti-TNF treatment and for 6 months after cessation 1
  • The majority of TB cases occur within three cycles of treatment (median 12 weeks), with extrapulmonary TB being common 1, 2
  • For patients at high risk (black Africans over 15 years, South Asians born outside UK), chemoprophylaxis should be considered before starting infliximab 1
  • Close cooperation between prescribing clinicians and TB specialists is strongly recommended 1

Laboratory Monitoring

  • Platelet counts should be regularly monitored as thrombocytopenia occurs in 1 in 500 to 1 in 1000 patients 1
  • Less frequent biochemistry and hematology monitoring is required compared to conventional drug therapies, but regular clinical review remains essential 1
  • Monitor C-reactive protein (CRP) levels as treatment with infliximab typically decreases serum levels 3

Clinical Response Assessment

  • Patients should be seen at 12 weeks to determine whether therapy should be continued, then at 3-6 month intervals 1
  • For psoriasis, adequate response is defined as ≥50% reduction in baseline PASI score and ≥5-point improvement in DLQI within 3 months 1
  • Therapy should be withdrawn if adequate response is not achieved after 3 months 1

Adverse Events Monitoring

  • Monitor for infusion reactions, which commonly include headache, fever, chills, and myalgia during the first few weeks of treatment 1
  • Watch for skin reactions, particularly a transient acute pruritic eruption between weeks 4-10 in flexural sites, arms, neck, and trunk 1
  • Monitor for serious infections, particularly tuberculosis, which may present atypically in patients on infliximab 2, 4
  • Be vigilant for signs of hepatotoxicity, serum sickness-like disease, and lymphoma 5

Special Considerations

  • Elderly patients have a higher incidence of infections and serious adverse reactions; more careful monitoring is required 3
  • For patients on concomitant immunosuppressants, tuberculin skin tests may be unreliable (false negative); risk assessment should be individualized 1, 6
  • If a patient's condition does not improve during treatment, always consider the possibility of tuberculosis infection 6
  • In areas with high TB burden, consider more frequent IGRA testing, especially during early treatment (first 40 weeks) 7

Overdose Management

  • If overdose occurs, monitor for signs or symptoms of adverse reactions and institute appropriate symptomatic treatment 3

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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