What additional baseline investigations are required before initiating secukinumab (Cosentyx) in a 10‑year‑old child with severe psoriasis vulgaris, beyond tuberculin skin test or chest radiograph, hepatitis B surface antigen and core antibody, hepatitis C antibody, HIV 1/2 antibody, complete blood count, renal and liver function tests, lipid profile, and review for inflammatory bowel disease symptoms?

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Last updated: October 5, 2026 • View editorial policy

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Baseline Investigations for Secukinumab in Pediatric Psoriasis

Your current pre-treatment workup is comprehensive and appropriate—no additional mandatory investigations are required beyond what you've already listed for a 10-year-old starting secukinumab for severe psoriasis vulgaris.

Current Standard of Care

The investigations you've outlined align with the 2020 Joint AAD-NPF pediatric psoriasis guidelines 1. The FDA label for secukinumab (Cosentyx) emphasizes TB screening and monitoring for infections but does not mandate additional baseline testing beyond standard infectious disease screening 2.

Your Complete Baseline Panel Includes:

  • Tuberculosis screening: Tuberculin skin test (PPD), QuantiFERON Gold, or T-Spot
  • Chest radiograph: For TB evaluation
  • Hepatitis panel: HBsAg, HBcAb (IgG), HCV antibody
  • HIV screening: HIV 1/2 antibody
  • Complete blood count with differential
  • Renal function tests
  • Liver function tests
  • Lipid profile
  • Clinical assessment for inflammatory bowel disease symptoms

Key Monitoring Considerations

Tuberculosis Screening Nuances

The 2020 guidelines specify that yearly TB testing is recommended for high-risk patients (those with TB exposure, travel history, or contact with active TB cases), but for average-risk pediatric patients, screening frequency is at the dermatologist's discretion 1. Unlike TNF-alpha inhibitors, IL-17A inhibitors like secukinumab carry lower TB reactivation risk 3.

Important caveat: QuantiFERON Gold can remain positive after latent TB treatment, so document baseline results carefully 1.

Hepatitis B Monitoring

While you're correctly screening for HBV, be aware that HBV reactivation can occur even with negative HBsAg if Anti-HBc IgG is positive 4. For patients with isolated Anti-HBc positivity (occult HBV), consider baseline HBV-DNA PCR and periodic monitoring during treatment, though this is not universally mandated 5, 4.

Inflammatory Bowel Disease Assessment

Your clinical screening for IBD symptoms is appropriate. Secukinumab carries a specific warning about new-onset or exacerbation of inflammatory bowel disease 2, 3. Document any history of abdominal pain, diarrhea, or bloody stools. No additional baseline colonoscopy or inflammatory markers are required unless symptoms are present.

What You Don't Need

Pregnancy Testing

Not applicable for your 10-year-old male patient, but document that children should be up-to-date on all non-live vaccines before starting secukinumab 2.

Baseline Immunoglobulin Levels

Not required—secukinumab does not cause hypogammaglobulinemia like some other immunosuppressants.

Baseline Candida Screening

Not indicated. While mild-to-moderate mucocutaneous candidiasis (oral/genital) is the most common infection with secukinumab, baseline screening is unnecessary 3, 6, 7.

Common Pitfalls to Avoid

  1. Don't delay treatment for chest X-ray if TB screening is negative and the patient is asymptomatic—chest radiography is discretionary per guidelines 1.

  2. Don't use secukinumab if active TB infection is present—this is an absolute contraindication 2.

  3. Don't forget to document latex allergy status—the Sensoready pen and prefilled syringe needle caps contain latex 2.

  4. Don't overlook growth parameters—the guidelines recommend monitoring growth in all pediatric patients on long-term systemic therapy 1.

Ongoing Monitoring After Initiation

Once treatment begins, no routine laboratory monitoring is required for secukinumab, unlike methotrexate or cyclosporine 1. Monitor clinically for:

  • Signs of infection (most common: nasopharyngitis, upper respiratory infections, candidiasis) 6, 7
  • New or worsening GI symptoms suggesting IBD
  • Efficacy measures (PASI scores, quality of life assessments)

The safety profile through 236 weeks in pediatric patients shows nasopharyngitis (13.9 per 100 patient-years), headache (5.8), and tonsillitis (4.7) as the most common adverse events, with only 3 cases of Candida infections reported 7.

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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.