The novel SCD MED ALERT mHealth app: empowering patients with sickle cell disease

Simone Villaboni , Valeria Maria Pinto , Barbara Gianesin , Maddalena Casale , Silverio Perrotta , Filippo Mazzi , Jacopo Ceolan , Roberto Pirrone , Paolo Cavellini , Antonia Gigante , Michaela Calvillo , Raffaella Origa , Gian Luca Forni , Lucia De Franceschi

Rare Disease and Orphan Drugs Journal ›› 2025, Vol. 4 ›› Issue (1) : 7

PDF
Rare Disease and Orphan Drugs Journal ›› 2025, Vol. 4 ›› Issue (1) :7 DOI: 10.20517/rdodj.2024.31
Original Article

The novel SCD MED ALERT mHealth app: empowering patients with sickle cell disease

Author information +
History +
PDF

Abstract

Aim: Sickle cell disease (SCD) is a debilitating monogenic disorder of red blood cells, characterized by acute pain episodes during vaso-occlusive crises (VOCs). Here, we developed and validated a medical app, SCD-MED-ALERT, for home management of acute pain in patients with SCD.

Methods: The SCD-MED-ALERT app is a multilingual and standalone application for iOS and Android. It was proposed to young adult patients with SCD (n = 47) attending comprehensive sickle cell centers within the Società Italiana Talassemie ed Emoglobinopatie (SITE) network. Patient-Activation-Measure-13 (PAM-13) questionnaire and mHealth App Usability Questionnaire (MAUQ) were used to evaluate patient activation levels in self-management and the app’s usability, respectively.

Results: Among SCD patients using SCD-MED-ALERT, the total PAM score significantly increased from 40 ± 4 (mean ± SD) to 42 ± 4 (P < 0.001). Multivariate analysis revealed that the baseline PAM score was positively associated with patients on crizanlizumab plus hydroxyurea therapy (P = 0.015), suggesting a higher sense of self-efficacy among those receiving combination treatment compared to those on hydroxyurea alone. A positive association was also observed between changes in PAM scores and patients undergoing chronic erythroexchange (P = 0.036). The MAUQ results showed a favorable consensus regarding the app’s usability, with a mean score of 5.9 ± 0.3, reflecting high usability. Overall, 31/44 (70%) responding patients used the app to report pain crises. Neither gender nor chronic pain treatment influenced the PAM scores at baseline or after app use.

Conclusion: Our study shows that the SCD-MED-ALERT app enhances patients’ sense of self-efficacy and proactivity in managing pain at home during acute pain crises. We propose that this app might contribute to empowering SCD patients and assist physicians in identifying patients who may benefit from more intensive treatment(s).

Keywords

Sickle cell disease / mHealth app / pain management / vaso-occlusive crisis / medical applications / MAUQ / PAM-13

Cite this article

Download citation ▾
Simone Villaboni, Valeria Maria Pinto, Barbara Gianesin, Maddalena Casale, Silverio Perrotta, Filippo Mazzi, Jacopo Ceolan, Roberto Pirrone, Paolo Cavellini, Antonia Gigante, Michaela Calvillo, Raffaella Origa, Gian Luca Forni, Lucia De Franceschi. The novel SCD MED ALERT mHealth app: empowering patients with sickle cell disease. Rare Disease and Orphan Drugs Journal, 2025, 4(1): 7 DOI:10.20517/rdodj.2024.31

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Piel FB,DeBaun MR.Defining global strategies to improve outcomes in sickle cell disease: a lancet haematology commission.Lancet Haematol2023;10:e633-86

[2]

Pinto VM,Quintino S.Sickle cell disease: a review for the internist.Intern Emerg Med2019;14:1051-64

[3]

Brousseau DC,Mosso AL,Steiner CA.Acute care utilization and rehospitalizations for sickle cell disease.JAMA2010;303:1288-94

[4]

Dampier C,Rhee S.Comprehensive Sickle Cell Centers (CSCC) Clinical Trial Consortium (CTC) Site InvestigatorsHealth-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium.Am J Hematol2011;86:203-5

[5]

Carroll CP,Fagan P.The course and correlates of high hospital utilization in sickle cell disease: evidence from a large, urban medicaid managed care organization.Am J Hematol2009;84:666-70 PMCID:PMC2783233

[6]

Ballas SK.Current issues in sickle cell pain and its management.Hematology Am Soc Hematol Educ Program2007;:97-105

[7]

Pinto VM,De Franceschi L.Novel therapeutic approaches in thalassemias, sickle cell disease, and other red cell disorders.Blood2024;144:853-66

[8]

Hebbel RP,Kaul D.The endothelial biology of sickle cell disease: inflammation and a chronic vasculopathy.Microcirculation2004;11:129-151.

[9]

Hebbel RP,Vercellotti GM.The multifaceted role of ischemia/reperfusion in sickle cell anemia.J Clin Invest2020;130:1062-72 PMCID:PMC7269579

[10]

Kalish BT,Andolfo I.Dietary ω-3 fatty acids protect against vasculopathy in a transgenic mouse model of sickle cell disease.Haematologica2015;100:870-80

[11]

Francis RB.Vascular occlusion in sickle cell disease: current concepts and unanswered questions.Blood1991;77:1405-1414

[12]

Field JJ,Campbell CM.AAAPT diagnostic criteria for acute sickle cell disease pain.J Pain2019;20:746-59

[13]

Boonstra AM,Köke AJ.Cut-off points for mild, moderate, and severe pain on the numeric rating scale for pain in patients with chronic musculoskeletal pain: variability and influence of sex and catastrophizing.Front Psychol2016;7:1466 PMCID:PMC5043012

[14]

Darbari DS.Pain-measurement tools in sickle cell disease: where are we now?.Hematology Am Soc Hematol Educ Program2017;2017:534-41 PMCID:PMC6142608

[15]

De Franceschi L,Schweiger V.Fentanyl buccal tablet: a new breakthrough pain medication in early management of severe vaso-occlusive crisis in sickle cell disease.Pain Pract2016;16:680-7

[16]

Hehn CA, Baron R, Woolf CJ. Deconstructing the neuropathic pain phenotype to reveal neural mechanisms.Neuron2012;73:638-52 PMCID:PMC3319438

[17]

Kehlet H.The value of “multimodal” or “balanced analgesia” in postoperative pain treatment.Anesth Analg1993;77:1048-56

[18]

Osunkwo I,Minniti CP.Impact of sickle cell disease on patients’ daily lives, symptoms reported, and disease management strategies: results from the international sickle cell world assessment survey (SWAY).Am J Hematol2021;96:404-17 PMCID:PMC8248107

[19]

Hanna M,Perrot S.Delivery of multimodal analgesia to effectively treat acute pain: a review from roma pain days.Cureus2022;14:e22465 PMCID:PMC8942173

[20]

Savarese JJ.Multimodal analgesia as an alternative to the risks of opioid monotherapy in surgical pain management.J Healthc Risk Manag2017;37:24-30

[21]

Knisely MR,Kroner B.Sickle Cell Disease Implementation ConsortiumPatient-reported outcomes in sickle cell disease and association with clinical and psychosocial factors: report from the sickle cell disease implementation consortium.Am J Hematol2020;95:1066-74

[22]

Haywood C Jr,Lanzkron S.A systematic review of barriers and interventions to improve appropriate use of therapies for sickle cell disease.J Natl Med Assoc2009;101:1022-33

[23]

Ji RR,Gao YJ.Emerging targets in neuroinflammation-driven chronic pain.Nat Rev Drug Discov2014;13:533-48 PMCID:PMC4228377

[24]

McClish DK,Bovbjerg VE.Health related quality of life in sickle cell patients: the PiSCES project.Health Qual Life Outcomes2005;3:50 PMCID:PMC1253526

[25]

Minniti C,Andemariam B. Use of opioids in patients with sickle cell disease (SCD): a country and age analysis of the international sickle cell world assessment survey (SWAY). https://library.ehaweb.org/eha/2020/eha25th/294008/caterina.minniti.use.of.opioids.in.patients.with.sickle.cell.disease.%28scd%29.a.html. [Last accessed on 17 Mar 2025]

[26]

Pinto VM,Sardo S.Safety and efficacy of ketorolac continuous infusion for multimodal analgesia of vaso-occlusive crisis in patients with sickle cell disease.Orphanet J Rare Dis2024;19:22 PMCID:PMC10801952

[27]

L DF,A V.A pilot study on the efficacy of ketorolac plus tramadol infusion combined with erythrocytapheresis in the management of acute severe vaso-occlusive crises and sickle cell pain.Haematologica2004;89:1389-91

[28]

Forni GL,Graziadei G.Development of interactive algorithm for clinical management of acute events related to sickle cell disease in emergency department.Orphanet J Rare Dis2014;9:91 PMCID:PMC4230640

[29]

Marcolino MS,D’Agostino M,Alkmim MBM.The impact of mHealth interventions: systematic review of systematic reviews.JMIR Mhealth Uhealth2018;6:e23 PMCID:PMC5792697

[30]

Moreno-Ligero M,Salazar A.mHealth intervention for improving pain, quality of life, and functional disability in patients with chronic pain: systematic review.JMIR Mhealth Uhealth2023;11:e40844 PMCID:PMC9936365

[31]

Piette JD,Krein SL.Patient-centered pain care using artificial intelligence and mobile health tools: a randomized comparative effectiveness trial.JAMA Intern Med2022;182:975-83 PMCID:PMC9361183

[32]

Shah N,De Castro L.Patients welcome the sickle cell disease mobile application to record symptoms via technology (SMART).Hemoglobin2014;38:99-103

[33]

Anderson LM,Jonassaint J,Bonner M.Mobile health intervention for youth with sickle cell disease: impact on adherence, disease knowledge, and quality of life.Pediatr Blood Cancer2018;65:e27081

[34]

Elander J,Kapadi R.Development and validation of the satisfaction with treatment for pain questionnaire (STPQ) among patients with sickle cell disease.Br J Haematol2019;187:105-16

[35]

Abrams C,Melvin C.Engagement with incharge app - a mobile health intervention to improve adherence to hydroxyurea among individuals with sickle cell disease.Blood2023;142:1144

[36]

Smith WR,Bovbjerg VE.Daily assessment of pain in adults with sickle cell disease.Ann Intern Med2008;148:94-101

[37]

Crosby LE,Goldstein A.Development and evaluation of iManage: a self-management app co-designed by adolescents with sickle cell disease.Pediatr Blood Cancer2017;64:139-45

[38]

Jonassaint CR,Jonassaint J.Usability and feasibility of an mHealth intervention for monitoring and managing pain symptoms in sickle cell disease: the sickle cell disease mobile application to record symptoms via technology (SMART).Hemoglobin2015;39:162-8

[39]

Crosby LE,Kidwell K.Improving self-management in adolescents with sickle cell disease.Pediatr Blood Cancer2020;67:e28492

[40]

Crosby LE,Joffe NE.Reply to iManage: a novel self-management app for sickle cell disease.Pediatr Blood Cancer2017;64 PMCID:PMC7323363

[41]

Wakefield D,Selman LE,Higginson IJ.Patient empowerment, what does it mean for adults in the advanced stages of a life-limiting illness: a systematic review using critical interpretive synthesis.Palliat Med2018;32:1288-304 PMCID:PMC6088522

[42]

Villaboni S,Casale M.SCD MED ALERT, a novel mHealth for acute pain management, contributes to the empowerment of patients with sickle cell disease.Blood2024;144:1140-1140

[43]

Forni G,Casale M. Algoritmo per la gestione in pronto soccorso degli eventi acuti nei pazienti affetti da anemia falciforme. Collana Scientifica SITE Opinione di esperti. 2019. Available from: http://www.site-italia.org/file/Triage_SCD.pdf. [Last accessed on 11 Mar 2025]

[44]

Graffigna G,Bonanomi A,Hibbard J.Measuring patient activation in Italy: translation, adaptation and validation of the Italian version of the patient activation measure 13 (PAM13-I).BMC Med Inform Decis Mak2015;15:109 PMCID:PMC4690217

[45]

Zhou L,Setiawan IMA,Parmanto B.The mHealth app usability questionnaire (MAUQ): development and validation study.JMIR Mhealth Uhealth2019;7:e11500 PMCID:PMC6482399

[46]

Visser E,Hoogenboom A.Prevalence and impact of fatigue in children with primary immunodeficiency disorders: a quantitative single-center study.J Clin Immunol2022;42:1223-9 PMCID:PMC9537115

[47]

Hengenius JB,Zhu X,Huppert TJ.Fatigue and perceived energy in a sample of older adults over 10 years: a resting state functional connectivity study of neural correlates.Exp Gerontol2024;188:112388

[48]

Gianesin B,Musallam KM.Italian Hemoglobinopathies National Survey GroupPrevalence and mortality trends of hemoglobinopathies in Italy: a nationwide study.Haematologica2025;

[49]

Xu JZ.The carrier state for sickle cell disease is not completely harmless.Haematologica2019;104:1106-11 PMCID:PMC6545856

[50]

Hibbard JH,Mahoney ER.Development of the patient activation measure (PAM): conceptualizing and measuring activation in patients and consumers.Health Serv Res2004;39:1005-26 PMCID:PMC1361049

[51]

Hibbard JH,Stockard J.Development and testing of a short form of the patient activation measure.Health Serv Res2005;40:1918-30 PMCID:PMC1361231

[52]

Green CA,Polen MR,Hibbard JH.Development of the patient activation measure for mental health.Adm Policy Ment Health2010;37:327-33 PMCID:PMC3536445

[53]

Packer TL,Ghahari S,Versnel J.The patient activation measure: a validation study in a neurological population.Qual Life Res2015;24:1587-96

[54]

Hussein WF,Carrasco A.Changes in patient activation in people starting dialysis: a prospective longitudinal, observational study.Hemodial Int2022;26:435-48 PMCID:PMC9546050

[55]

Lara-Cabrera ML,Nesset MB,Iversen VC.The effect of a brief educational programme added to mental health treatment to improve patient activation: a randomized controlled trial in community mental health centres.Patient Educ Couns2016;99:760-8

[56]

Gagnon J,Chartrand J.mHealth app usability questionnaire for stand-alone mHealth apps used by health care providers: canadian French translation, cross-cultural adaptation, and validation (Part 1).JMIR Form Res2024;8:e50839 PMCID:PMC10900083

[57]

Petracca F,Cucciniello M.An electronic patient-reported outcome mobile app for data collection in type a hemophilia: design and usability study.JMIR Form Res2021;5:e25071 PMCID:PMC8686465

[58]

McClish DK,Dahman BA.Pain site frequency and location in sickle cell disease: the PiSCES project.Pain2009;145:246-51 PMCID:PMC2771372

[59]

Taylor LE,Humphreys J,Miaskowski C.A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease.J Pain Symptom Manage2010;40:416-35 PMCID:PMC2989986

[60]

Rees DC,Unal S.A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemia.Blood2022;139:2642-52

[61]

Azizoddin DR,Kessler D.Leveraging mobile health technology and research methodology to optimize patient education and self-management support for advanced cancer pain.Support Care Cancer2021;29:5741-51 PMCID:PMC8410657

[62]

Costa E,de Montalembert M,Ware RE.Successes and pitfalls in orphan drug development for sickle cell disease.Blood Adv2024;8:2455-65 PMCID:PMC11112610

[63]

Sop DM,Zhang Y,Wilson J.Feasibility and quality validation of a mobile application for enhancing adherence to opioids in sickle cell disease.Healthcare2022;10:1506 PMCID:PMC9407817

[64]

Dunsmuir D,Sun T.A postoperative pain management mobile app (panda) for children at home after discharge: usability and feasibility.JMIR Perioper Med2019;2:e12305 PMCID:PMC7709843

[65]

Chakravorty S,Witwicki C.Patient-reported experience measure in sickle cell disease.Arch Dis Child2018;103:1104-9 PMCID:PMC6287562

[66]

Clayton JM,Tattersall MH.Randomized controlled trial of a prompt list to help advanced cancer patients and their caregivers to ask questions about prognosis and end-of-life care.J Clin Oncol2007;25:715-23

[67]

Richardson K,MacLeod R.Ever decreasing circles: terminal illness, empowerment and decision-making.J Prim Health Car2:130-5.

[68]

Olsman E,Leget C.Solicitude: balancing compassion and empowerment in a relational ethics of hope-an empirical-ethical study in palliative care.Med Health Care Philos2016;19:11-20

[69]

Smith WR,Penberthy LT.Understanding pain and improving management of sickle cell disease: the PiSCES study.J Natl Med Assoc2005;97:183-93 PMCID:PMC2568749

AI Summary AI Mindmap
PDF

79

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/