» Articles » PMID: 37991760

Use of Disease-Modifying Treatments in Patients With Sickle Cell Disease

Overview
Journal JAMA Netw Open
Specialty General Medicine
Date 2023 Nov 22
PMID 37991760
Authors
Affiliations
Soon will be listed here.
Abstract

Importance: Despite hydroxyurea being an established treatment for sickle cell disease (SCD), it remains underused. The recent approval of the disease-modifying treatments (DMTs) l-glutamine, crizanlizumab, and voxelotor underscores the need to understand the uptake of DMTs in the current treatment landscape.

Objective: To explore characteristics that may be associated with DMT use and to describe observed patterns of yearly DMT use from 2014 to 2021.

Design, Setting, And Participants: This cross-sectional study used administrative claims data from Optum's deidentified Clinformatics Data Mart Database from January 1, 2014, to September 30, 2021, to identify adults and children with SCD. Data were analyzed from August 1, 2022, to August 28, 2023.

Exposure: Use of DMTs.

Main Outcomes And Measures: Patient characteristics across groups with varying patterns of DMT use and yearly patterns of prescription fills for hydroxyurea, crizanlizumab, voxelotor, and l-glutamine.

Results: A total of 5022 beneficiaries with SCD (2081 [41.4%] aged 18-45 years; 2929 [58.3%] female) were included in sample A (144 [2.9%] inconsistent users, 274 [5.5%] incident users, 892 [17.8%] consistent users, and 3712 [73.9%] non-DMT users). Inconsistent users had a higher prevalence of vaso-occlusive crises (mean [SD], 3.7 [4.7]), splenic complications (6 of 144 [4.2%]), pulmonary complications (36 of 144 [25.0%]), kidney disease (21 of 144 [14.6%]), acute chest syndrome (18 of 144 [12.5%]), and health care visits (eg, mean [SD] inpatient visits, 7.0 [10.7]) compared with the other use groups. Non-DMT users had the lowest prevalence of vaso-occlusive crises (mean [SD], 0.8 [2.4]), acute chest syndrome (109 of 3712 [2.9%]), and inpatient (mean [SD], 2.0 [6.6]) and emergency department (mean [SD], 0.7 [3.1]) visits and the highest proportion of adults 65 years and older (593 of 3712 [16.0%]). In sample B (6387 beneficiaries with SCD), hydroxyurea use modestly increased from 428 of 2188 participants (19.6%) in 2014 to 701 of 2880 (24.3%) in 2021. Use of l-glutamine increased briefly but gradually decreased throughout the study period. In 2021, out of 2880 participants, 102 (3.5%) had at least 1 fill for crizanlizumab and 131 (4.6%) had at least 1 fill for voxelotor. Overall, total DMT use increased from 428 of 2188 participants (19.6%) in 2014 to 815 of 2880 patients (28.3%) in 2021.

Conclusions And Relevance: In this cross-sectional analysis of adults and children with SCD, uptake of DMTs remained low from 2014 to 2021, despite the approval of newer therapies. Notable differences in patient characteristics across varied DMT exposure types necessitate further exploration into factors that facilitate DMT use and the creation of strategies to enhance DMT uptake.

Citing Articles

The Current Role of Hydroxyurea in the Treatment of Sickle Cell Anemia.

Lopez Rubio M, Arguello Marina M J Clin Med. 2024; 13(21).

PMID: 39518543 PMC: 11546997. DOI: 10.3390/jcm13216404.


Opioid-related emergency admissions in people with opioid dependence/use disorder with and without sickle cell disease: An analysis of multi-state insurance claims.

Liu S, Brown T, King A, Lin L, Rehman S, Grucza R Gen Hosp Psychiatry. 2024; 91:83-88.

PMID: 39378616 PMC: 11634658. DOI: 10.1016/j.genhosppsych.2024.09.013.


Newer Modalities and Updates in the Management of Sickle Cell Disease: A Systematic Review.

Patel Z, Prajjwal P, Bethineedi L, Patel D, Khullar K, Patel H J Blood Med. 2024; 15:435-447.

PMID: 39286637 PMC: 11404495. DOI: 10.2147/JBM.S477507.


Modulation of the allosteric and vasoregulatory arms of erythrocytic oxygen transport.

Wise T, Ott M, Joseph M, Welsby I, Darrow C, McMahon T Front Physiol. 2024; 15:1394650.

PMID: 38915775 PMC: 11194670. DOI: 10.3389/fphys.2024.1394650.

References
1.
Yawn B, Buchanan G, Afenyi-Annan A, Ballas S, Hassell K, James A . Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members. JAMA. 2014; 312(10):1033-48. DOI: 10.1001/jama.2014.10517. View

2.
Kavanagh P, Fasipe T, Wun T . Sickle Cell Disease: A Review. JAMA. 2022; 328(1):57-68. DOI: 10.1001/jama.2022.10233. View

3.
Manwani D, Burnett A, Paulose J, Yen G, Burton T, Anderson A . Treatment patterns and burden of complications associated with sickle cell disease: A US retrospective claims analysis. EJHaem. 2022; 3(4):1135-1144. PMC: 9713207. DOI: 10.1002/jha2.575. View

4.
Mainous 3rd A, Tanner R, Harle C, Baker R, Shokar N, Hulihan M . Attitudes toward Management of Sickle Cell Disease and Its Complications: A National Survey of Academic Family Physicians. Anemia. 2015; 2015:853835. PMC: 4352517. DOI: 10.1155/2015/853835. View

5.
Shah N, Bhor M, Xie L, Halloway R, Arcona S, Paulose J . Treatment patterns and economic burden of sickle-cell disease patients prescribed hydroxyurea: a retrospective claims-based study. Health Qual Life Outcomes. 2019; 17(1):155. PMC: 6794855. DOI: 10.1186/s12955-019-1225-7. View