First-person perspective: Russian practice of replacement therapy — patients' experience

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Abstract

BACKGROUND: Normal human immunoglobulin replacement therapy is the "gold standard" for treating antibody synthesis deficiency. Intravenous immunoglobulin improved patient survival, while subcutaneous immunoglobulin reduced adverse events and improved quality of life. The lack of objective statistics in Russia on immunoglobulin availability and its impact on adult patients' social activity necessitated this study.

AIM: To analyze adult patients' subjective assessment of subcutaneous and intravenous immunoglobulin forms for replacement therapy.

METHODS: The study included patients over 18 years of age with inborn errors of immunity and recommended replacement therapy. Participants completed an online questionnaire containing questions about disease history, quality of replacement therapy provision, tolerability, and personal preferences. The survey was conducted from April to August 2025. Pearson's χ2 and Mann–Whitney U tests were used for statistical analysis. The level of statistical significance was p < 0.05.

RESULTS: The survey involved 200 patients: 26 receiving subcutaneous immunoglobulin therapy, 158 receiving intravenous immunoglobulin, and 16 patients were not provided with medications. Subcutaneous immunoglobulin therapy showed advantages in terms of: the number of antibiotic therapy episodes (p = 0.048), presence of adverse reactions (p = 0.038), number of hospital days per month per patient (0.38 vs. 1.83, p < 0.001), and days of disability per year per working patient (0.5 vs. 1.46, p = 0.049), and regularity of drug provision (p = 0.003). 56.52 % of respondents had restrictions on intravenous immunoglobulin therapy (venous access difficulties, comorbidities). Individuals with established disabilities have a better provision profile: 76.5 % of patients receive the drug regularly (87.7 % in full dose), while those without federal benefits receive it in 23.8 % of cases (42.9 % in full dose) (p < 0.001 and p < 0.001, respectively).

CONCLUSION: The lack of federal benefits complicates patients' access to medications, prioritizing drug availability over quality of life. Russia lacks pharmacoeconomic studies evaluating immunoglobulin therapy effectiveness, highlighting the need for new therapy approaches and improved patient care systems. Expanding subcutaneous immunoglobulin use could address remote region therapy challenges, reduce outpatient clinic loads, lower inpatient care costs, and lessen disease impact on patients' lives.

About the authors

Gulnara G. Suleymanova

National Research Center — Institute of Immunology Federal Medical-Biological Agency; Medsi Clinical Diagnostic Center in Shchelkovo

Author for correspondence.
Email: sulejmanova653@gmail.com
ORCID iD: 0009-0001-2191-435X
Russian Federation, Moscow; Shchelkovo, Moscow Region

Nikolay A. Nazarov

National Research Center — Institute of Immunology Federal Medical-Biological Agency

Email: 5898050@gmail.com
ORCID iD: 0009-0000-0445-0533
Russian Federation, Moscow

Evgeniy A. Frolov

National Research Center — Institute of Immunology Federal Medical-Biological Agency

Email: frolovevgeny@rambler.ru
ORCID iD: 0000-0002-0800-5960
SPIN-code: 5963-4062
Russian Federation, Moscow

Tatiana V. Nekrasova

National Research Center — Institute of Immunology Federal Medical-Biological Agency

Email: loriley@mail.ru
ORCID iD: 0009-0002-4837-6624
SPIN-code: 8290-3584
Russian Federation, Moscow

Tatiana S. Romanova

National Research Center — Institute of Immunology Federal Medical-Biological Agency

Email: ts_romanova@mail.ru
ORCID iD: 0000-0003-3350-3811
SPIN-code: 8027-8625

MD, Cand. Sci. (Medicine)

Russian Federation, Moscow

Tatiana N. Myasnikova

National Research Center — Institute of Immunology Federal Medical-Biological Agency

Email: t_miasnikova@mail.ru
ORCID iD: 0000-0001-8491-195X
SPIN-code: 4684-3112

MD, Cand. Sci. (Medicine)

Russian Federation, Moscow

Ekaterina N. Medunitsyna

National Research Center — Institute of Immunology Federal Medical-Biological Agency; Russian University of Medicine

Email: medunitsyna.kate@yandex.ru
ORCID iD: 0000-0002-7872-6261
SPIN-code: 6633-7370

MD, Cand. Sci. (Medicine)

Russian Federation, Moscow; Moscow

Tatiana V. Latysheva

National Research Center — Institute of Immunology Federal Medical-Biological Agency; Russian University of Medicine

Email: tvlat@mail.ru
ORCID iD: 0000-0003-1508-0640
SPIN-code: 8929-7644

MD, Dr. Sci. (Medicine), Professor

Russian Federation, Moscow; Moscow

Elena A. Latysheva

National Research Center — Institute of Immunology Federal Medical-Biological Agency; Russian National Research Medical University named after N.I. Pirogov

Email: ealat@mail.ru
ORCID iD: 0000-0002-1606-205X
SPIN-code: 2063-7973

MD, Dr. Sci. (Medicine)

Russian Federation, Moscow; Moscow

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