Clinical Validation of a Capillary Blood Home-Based Self-Sampling Technique for Monitoring of Infliximab, Vedolizumab, and C-Reactive Protein Concentrations in Patients With Inflammatory Bowel Disease

Author:

Otten Antonius T1ORCID,van der Meulen Hedwig H1,Steenhuis Maurice2,Loeff Floris C2,Touw Daan J3ORCID,Kosterink Jos G W4,Frijlink Henderik W5,Rispens Theo6,Dijkstra Gerard1,Visschedijk Marijn C1,Bourgonje Arno R1ORCID

Affiliation:

1. Department of Gastroenterology and Hepatology, University Medical Centre Groningen , Groningen , the Netherlands

2. Biologics Laboratory, Sanquin Diagnostic Services , Amsterdam , the Netherlands

3. Department of Pharmaceutical Analysis, Groningen Research Institute of Pharmacy, University of Groningen , Groningen , the Netherlands

4. Department of PharmacoTherapy, Epidemiology and Economy, Groningen Research Institute of Pharmacy, University of Groningen , Groningen , the Netherlands

5. Department of Pharmaceutical Technology and Biopharmacy, Groningen Research Institute of Pharmacy, University of Groningen , Groningen , the Netherlands

6. Department of Immunopathology, Sanquin Research , Amsterdam , the Netherlands

Abstract

Abstract Background Therapeutic drug monitoring provides important guidance for treatment of patients with inflammatory bowel disease (IBD) and could help to early identify treatment failure. This study aimed to validate a finger prick–based capillary blood sampling technique to measure biological trough levels and C-reactive protein (CRP) and evaluate patient performance and -support. Methods In this prospective cohort study, patients with IBD receiving infliximab (IFX) or vedolizumab (VEDO) therapy performed finger prick–based capillary blood sampling at home. Additionally, blood was collected through routinely performed in-hospital venepuncture prior to biological infusion. IFX, VEDO, and CRP concentrations were measured by enzyme-linked immunosorbent assay. The concordance between methods was statistically evaluated and a survey was conducted to assess practicality and patient support. Results In total, 81 patients (46 IFX, 35 VEDO) were enrolled. Mean differences between both methods were 0.42 (95% confidence interval, -1.74 to 2.58) μg/mL for IFX and 0.72 (95% confidence interval, -5.50 to 6.94) μg/mL for VEDO. Passing-Bablok regressions demonstrated no evidence for systematic or proportional biases. Venous and capillary IFX (ρ = 0.96, P < .001) and VEDO (ρ = 0.97, P < .001) levels strongly correlated and showed high intermethod agreement (Cohen’s kappa: IFX = 0.82; VEDO = 0.94). Similarly, venous and capillary CRP levels were strongly correlated (ρ = 0.99, P < .001). Most patients (>95%) were able to successfully perform the self-sampling at home without prior instructions. Conclusions This study clinically validated a finger prick–based capillary blood self-sampling technique allowing concomitant home monitoring of biological levels and CRP for patients with IBD, who reported substantial support, tolerability, and practicality.

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

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