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Intravenous human immunoglobulin utilization patterns and cost analysis in a Malaysian tertiary referral hospital

Abstract

Introduction

While intravenous human immunoglobulin therapy is potentially lifesaving for rare diseases, the significant costs associated with its usage warrant due attention. This study evaluated the costs and prescribing patterns of IVIg.

Methods

This was a retrospective analysis of medical records in a tertiary hospital. The evidence category IIA and below, as well as strength of recommendations level B and below were classified as lower evidence category and lower strength of recommendation, respectively. Patients’ demographic data, indications, dosing regimen, physician specialty were retrieved from medical records, while the cost was derived based on total prescribed doses.

Results

Out of 78 patients, more than half of the patients were prescribed with off-label IVIg based on MOHM Formulary (52, 66.7%), FDA indications (52, 66.7%) and EMA indications (46, 59.0%). 37 (47.4%) cases used IVIg for indications with lower evidence category and 52 (66.7%) cases with lower strength of recommendation. The total cost of IVIg use within the 2-year period was RM 695,426.36, with RM267,993.40 (38.5%) spent for indications with lower evidence category. Immunoglobulin use in rheumatology and neurology cases were associated with lower evidence category (p < 0.001).

Conclusions

A high proportion of off-label immunoglobulin use was observed. A timely update of prescribing policy, standardization of prescribing guidelines may promote appropriate immunoglobulin prescribing and justify expenses.

Background

Intravenous immunoglobulin (IVIg) is a blood product derived from human donor blood that contains a mixture of antibodies (immunoglobulins) in the form of preparation for intravenous injection. IVIg was initially used as a treatment for immune deficiencies, and later for various autoimmune and inflammatory disorders. Currently, there are ten approved indications for the use of IVIg, as established by the United States Food and Drug Administration (FDA) and European Medicines Agency (EMA) [1, 2].

Although manufacturing steps have been implemented to enhance the purity of the Immunoglobulin G molecules [3], its administration can lead to adverse events and potential fatal consequences. While IVIg therapy can be lifesaving for specific rare diseases, the significant costs associated with its usage warrant due attention. The total cost of IVIg usage may vary depending on several factors, such as the indication, duration of treatment and the patient’s body weight. In a utilisation review carried out in a tertiary care hospital in United Arab Emirates, the estimated annual cost of IVIg was US$1.25 million, in which US$0.7 million was associated with off-label indications [4]. In the USA, the average cost per IVIg infusion for chronic inflammatory demyelinating polyneuropathy was US$9720 [5].

In year 2000, Chen and colleagues reported that 52% of the study subjects from twelve institutions were treated with IVIg for off-label indications. Notably, no positive clinical outcome was observed among 12% in the label group and 20% in the off-label group [6]. Even though off-label indications were supported by limited evidence, there were over 150 off-label indications practiced among the prescribers, incurring substantial cost to the healthcare system [7].

Within the local context, two brands of IVIg with the proprietary name of Intragram® (6 g of human protein IgG in 100 ml) and Flebogamma® (10 g of human protein IgG in 100 mL). were listed in the formulary. Currently, more than three-fourth of the local IVIg was supplied by the National Blood Centre, with a subsidized cost of RM 200 per vial, and an actual cost of RM 500 per vial.

Prescribing of IVIg is primarily guided by the Ministry of Health Drug Formulary, but reference were rarely made to FDA, EMA, American Academy of Allergy, Asthma, and Immunology (AAAAI) evidence category and strength of recommendations for off-label use. There was a paucity of studies on the IVIg prescribing patterns and costs across different groups of patients and prescribers in Malaysia. Hence, this study aimed to evaluate the costs and prescribing patterns of IVIg in term of indications, off-label use, evidence level and strength of recommendation based on established guidelines.

Methods

This was a retrospective study conducted by the Pharmacy Department of Hospital Taiping, Malaysia. In this study, consecutive sampling method was employed. All neonatal, paediatric and adult patients who received IVIg treatment between 1st January 2019 and 31st December 2020 were included. Patients with untraceable medical records were excluded.

From the IVIg registry, a total of 91 patients prescribed with IVIg within the study period were identified. Patients’ demographic data, indications and dosing regimen of IVIg as well as physician specialty who prescribed IVIg were collected from the medical record office. The cost of IVIg was obtained from the supplier.

The indications of IVIg were compared to the indications approved by MOHM [8], FDA [1] and EMA [2]. Off-label indication was defined as IVIg use in any clinical conditions other than those approved by these three authorities. The evidence category and strength of recommendations for each indication were labelled according to the 2017 Update on the Use of Immunoglobulin in Human Disease: A review of evidence (Additional file 1: Tables S1 and S2) [9]. The evidence category IIA and below, as well as strength of recommendations level B and below were classified as lower evidence category and lower strength of recommendation, respectively.

SPSS version 26 (SPSS®, Chicago, IL) was used to perform all the statistical analyses. The cost and utilization of IVIg in accordance to evidence category and strength of recommendation were descriptively analyzed. The Chi Square test was used to determine the association between off-label use, indications and physician specialty with the evidence category and strength of recommendation. All statistical tests were two-tailed. A p value of <0.05 denoted statistical significance.

This study was registered in the National Medical Research Registry (NMRR-21-853-59575) and ethical approval for this study was obtained from the Medical Research and Ethics Committee (MREC), Ministry of Health Malaysia

Results

Initially, 91 patients were included in this study. Only 78 patients were eligible for analysis as 13 patients had untraceable medical records. Intragram® was used in 76 cases, while Flebogamma® in two cases. Majority were female (n = 57, 57.7%) and adult (n = 52, 66.7%). The median treatment duration was 2 days and the median total IVIg dose administered per patient was 54.0 gram. More than half of the patients were prescribed with off-label IVIg based on MOHM Formulary (52, 66.7%), FDA indications (52, 66.7%) and EMA indications (46, 59.0%). There were 37 (47.4%) cases which used IVIg for indications with lower evidence category and 52 (66.7%) cases with lower strength of recommendation (Table 1).

Table 1 Characteristics of patients and prescribing patterns (n = 78)

Chi-square test was performed and it was found that IVIg use in systemic lupus erythematosus (SLE) (9, 11.5%) and neonatal jaundice secondary to isoimmunehaemolytic disease (IHD) (9, 11.5%) were associated with lower evidence category (p < 0.001). Besides, IVIg prescribing by rheumatology (12, 15.4%) and neurology (20, 25.6%) were associated with lower evidence category (p < 0.001) as well as lower strength of recommendation (p < 0.001).

The total cost of IVIg use within the 2-year period was RM 695,426.36. In terms of physician specialty, neurology spent the most (RM 356,189.96), followed by rheumatology (RM 142,665.40), hematology (RM 88,401.00), pediatrics (RM 36,927.00), dermatology (RM 29,094.00), medical (RM 23,126.00) and intensive care unit (ICU) (RM 19,023.00). Based on indications, myasthenia gravis reported the highest cost (RM 121,598.00, n = 9), followed by SLE (RM 112,825.40, n = 9), severe refractory idiopathic thrombocytopenic purpura (ITP) (RM 88,774.00, n = 10) and Guillain–Barre syndrome (RM 88,401.00, n = 6) (Table 2). The total cost spent on indications with lower evidence category was RM267,993.40, whereby RM71,616.00 was spent on diagnoses with no established evidence support (Fig. 1 and Additional file 1: Table S3).

Table 2 Total cost of IVIg use on indications based on evidence category
Fig. 1
figure 1

Total cost based on evidence category

Discussion

In this study, more than half of the IVIg treatment were prescribed for off-label indications. A study on IVIg prescribing patterns in four teaching hospitals in Toronto revealed that over 80% of the patients received IVIg for indications supported by published recommendations [10]. On the other hand, 47.5% of the cases in this study fell under lower evidence category. Conversely, a study from Spain reported that 86% of the IVIg prescribed were for labelled indications, 10% were for off-label but scientifically supported indications, and only 4% were for off-label unsupported indications [11]. This suggests rational use of IVIg is possible with strict adherence to the labelled indications and diagnostic criteria.

IVIg recorded the highest single-drug expenditure in the studied period. The total cost of IVIg use was RM 695,426.36, noting that this was partially subsidized by the National Blood Centre. The actual unsubsidized projected cost of IVIg may exceed RM 900,000, a substantial amount which could be used for other therapeutic causes. Meanwhile, 38.5% of the total cost was spent on indications in lower evidence category and this imposed a huge cost burden on the hospital. Meanwhile, a previous study in Saudi Arabia by Alangari and colleagues revealed that IVIg was used as off-label or non-recommended indications among two-third of the population, incurring a cost of $431,325. [12]. The exorbitant costs of off-label and non-recommended IVIg use warrants evidence-based prescribing in clinical practice.

Although the use of IVIg treatment for septicaemia in immunocompromised patient is an approved indication in the MOHM Formulary, it has mixed evidence. Due to weak evidence of efficacy from previous studies, International Guidelines for Management of Sepsis and Septic Shock recommended against the use of IVIg in sepsis [13]. Jarczak and colleagues argued that IVIg appeared to be a safe treatment option for sepsis and septic shock, but further clinical data is required to assess the cost–benefit ratio [14]. Thus, the use of IVIg for septicaemia in immunocompromised patients should be constantly reviewed and evaluated based on current guidelines and evidence.

While the use of IVIg in treating Kawasaki disease was classified as high evidence according to American Academy of Allergy, Asthma and immunology [9], its use was not indicated in the local formulary. Timely review of IVIg use policy and development of national IVIg prescribing protocol based on updated evidence may provide guidance and standardization of IVIg usage across nationwide health facilities in the future.

In our study, the use of IVIg in nine SLE cases had costed RM 113,000. However, the use of IVIg in SLE was classified as lower evidence category. A reduction of the SLE disease activity index score suggested the beneficial effects of IVIg therapy [15]. IVIg was found to be beneficial in specific clinical manifestations of SLE including nephritis, cerebral lupus and serositis [16]. Hence, the use of IVIg in SLE should be decided on a case by case basis, prioritized based on clinical manifestations with proven efficacies.

Despite its high cost, IVIg played important role when no other cost-effective alternative available. For instance, the usage of IVIg in primary immunodeficiency with hypogammaglobulinemia may reduce mortality and morbidity, along with improved quality of life [17]. Meanwhile, the use of high-dose IVIg in ITP was established more than two decades ago [18]. Nevertheless, a recent review of recent evidence showed that eltrombopag, a non-peptide thrombopoietin appeared to be more cost-effective than IVIg treatment [19]. Similarly, newer options such as subcutaneous immunoglobulin and corticosteroids was found to be comparable to IVIg which was once known to be the only effective agent in treating CIDP [20]. A timely review of latest evidence is, therefore, warranted to inform and update current IVIg prescribing guidelines.

There were several limitations in this study. First, there was several medical records that could not be traced, and the actual usage could be higher than that reported. Second, records of outpatient IVIg use were not collected. As IVIg is often administered on an outpatient basis, future research should include this setting. Third, the small sample size has attributed to the short study duration. A longer study period with a larger sample size would improve generalizability of findings. Furthermore, we did not measure the clinical outcome of each case and hence calculation of incremental cost-effectiveness (ICER) ratio was not performed. This should be considered in future studies.

Conclusions

The majority of IVIg in this study was prescribed for off-label use. A timely revision of IVIg use policy, as well as the establishment of a national IVIg prescribing guideline may provide standardization in its usage and encourage evidence-based prescribing of IVIg.

Availability of data and materials

The data sets generated and/or analyzed during the current study are not publicly available due to confidentiality of patients, but are available from the corresponding author on reasonable request.

References

  1. United States Food & Drug Administration (FDA). Immune Globulin Intravenous (IGIV) Indications. https://www.fda.gov/vaccines-blood-biologics/approved-blood-products/immune-globulin-intravenous-igiv-indications. Accessed 28 Nov 2021.

  2. Committee for Medicinal Products for Human Use (CHMP). Guideline on the clinical investigation of human normal immunoglobulin for intravenous administration (IVIg) rev 3. European Medicines Agency. 2018. https://www.ema.europa.eu/en/clinical-investigation-human-normal-immunoglobulin-intravenous-administration-ivig. Accessed 28 Nov 2021.

  3. Bichuetti-Silva DC, Furlan FP, Nobre FA, Pereira CT, Gonçalves TR, Gouveia-Pereira M, et al. Immediate infusion related adverse reactions to intravenous immunoglobulin in a prospective cohort of 1765 infusions. Int Immunopharmacol. 2014;23(2):442–6.

    Article  CAS  Google Scholar 

  4. Dawoud T, Tatari H, Gebran N. A utilisation review of intravenous immunoglobulin in a tertiary care hospital in United Arab Emirates. Eur J Hosp Pharm Sci Pract. 2012;19(3):286–8.

    Article  Google Scholar 

  5. Burt RK, Tappenden P, Balabanov R, et al. The cost effectiveness of immunoglobulin vs hematopoietic stem cell transplantation for CIDP. Front Neurol. 2021;2021(12): 645263.

    Article  Google Scholar 

  6. Chen C, Danekas LH, Ratko TA, Vlasses PH, Matuszewski KA. A multicenter drug use surveillance of intravenous immunoglobulin utilization in US Academic Health Centers. Ann Pharmacother. 2000;2000(34):295–9.

    Article  Google Scholar 

  7. Fakhari Z, Farsaei S, Sabzghabaee AM. Predicting factors for the pattern of intravenous immunoglobulin utilization in a Middle Eastern University Hospital. J Res Pharm Pract. 2018;7(4):188–94.

    Article  Google Scholar 

  8. MOHM Formulary. https://www.pharmacy.gov.my/v2/en/apps/fukkm?generic=human+&category=&indications=

  9. Perez EE, Orange JS, Bonilla F, Chinen J, Chinn IK, Dorsey M, El-Gamal Y, Harville TO, Hossny E, Mazer B, Nelson R. Update on the use of immunoglobulin in human disease: a review of evidence. J Allergy Clin Immunol. 2017;139(3):S1–46.

    Article  CAS  Google Scholar 

  10. Pendergrast JM, Sher GD, Callum JL. Changes in intravenous immunoglobulin prescribing patterns during a period of severe product shortages, 1995–2000. Vox Sang. 2005;89(3):150–60.

    Article  CAS  Google Scholar 

  11. Badia M, Cardona L, Massanes R. Changes in the pattern of intravenous immunoglobulin use over a 5-year period. Eur J Hosp Pharm. 2006;2006(12):67–71.

    Google Scholar 

  12. Alangari AA, Abutaleb MH, Albarraq AA, et al. Intravenous immunoglobulin utilization in a tertiary care teaching hospital in Saudi Arabia. Saudi Med J. 2008;29(7):975–9.

    PubMed  Google Scholar 

  13. Rhodes A, Evans LE, Alhazzani W, et al. Surviving sepsis campaign: International Guidelines for Management of Sepsis and Septic Shock: 2016. Intensive Care Med. 2017. https://doi.org/10.1007/s00134-017-4683-6.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Jarczak D, Kluge S, Nierhaus A. Use of intravenous immunoglobulins in sepsis therapy—a clinical view. Int J Mol Sci. 2020;2020(21):5543.

    Article  Google Scholar 

  15. Justiz Vaillant A. A female with systemic lupus erythematosus and Streptococcal pneumonia treated with intravenous immunoglobulins (IVIg). Preprints 2020, 2020090544. https://doi.org/10.20944/preprints202009.0544.v1

  16. Zandman-Goddard G, Levy Y, Shoenfeld Y. Intravenous immunoglobulin therapy and systemic lupus erythematosus. Clin Rev Allergy Immunol. 2005;29:219–28.

    Article  CAS  Google Scholar 

  17. Fried AJ, Bonilla FA. Pathogenesis, diagnosis, and management of primary antibody deficiencies and infections. Clin Microbiol Rev. 2009;22(3):396–414. https://doi.org/10.1128/CMR.00001-09.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Jin F, Balthasar JP. Mechanisms of intravenous immunoglobulin action in immune thrombocytopenic purpura. Hum Immunol. 2005;66(4):403–10. https://doi.org/10.1016/j.humimm.2005.01.029.

    Article  CAS  PubMed  Google Scholar 

  19. Kaur MN, Arnold DM, Heddle NM, Cook RJ, Hsia C, Blostein M, Jamula E, Sholzberg M, Lin Y, Kassis J, Larratt L, Tinmouth A, Carruthers J, Li N, Liu Y, Xie F. Cost-effectiveness of eltrombopag vs intravenous immunoglobulin for the perioperative management of immune thrombocytopenia. Blood Adv. 2022;6(3):785–92. https://doi.org/10.1182/bloodadvances.2021005627.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Castle D, Robertson NP. Alternatives to intravenous immunoglobulin treatment in chronic inflammatory demyelinating polyradiculoneuropathy. J Neurol. 2019;266(9):2338–40. https://doi.org/10.1007/s00415-019-09485-9.

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

We would like to thank the Director General of Health Malaysia for his permission to publish this article.

Funding

This is a self-funded work.

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Authors and Affiliations

Authors

Contributions

SJC and CTC initiated the idea of this research work and drafted the proposal. SJC, CZN, YJO participated in data collection part. CZN, YJO performed data entry of the collected data. SJC, CZN, YJO, CTC contributed to the data analysis and manuscript drafting. KSKB reviewed the manuscript and provided administrative support and supervision. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Chee Tao Chang.

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Ethical approval for this study was obtained from the Medical Research and Ethics Committee (MREC), Ministry of Health Malaysia. Consent to participate was waived by the MREC.

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Editorial responsibility: Zaheer Babar, University of Huddersfield, UK.

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Supplementary Information

Additional file 1: Table S1.

IVIg approved indications based on MOHM, FDA, EMA and AAAAI evidence categories. Table S2. Definition on evidence category and strength of recommendation. Table S3. Total expenditures for indications in which evidence for its use was not established

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Choo, S.J., Ng, C.Z., Ong, Y.J. et al. Intravenous human immunoglobulin utilization patterns and cost analysis in a Malaysian tertiary referral hospital. J of Pharm Policy and Pract 15, 31 (2022). https://doi.org/10.1186/s40545-022-00430-2

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