Electronic Health Record-Embedded Individualized Pain Plans for Emergency Department Treatment of Vaso-occlusive Episodes in Adults With Sickle Cell Disease: Protocol for a Preimplementation and Postimplementation Study

Lingzi Luo, Allison A King, Yvonne Carroll, Ana A Baumann, Donald Brambilla, Christopher R Carpenter, Joseph Colla, Robert W Gibson, Siera Gollan, Greg Hall, Lisa Klesges, Abdullah Kutlar, Matthew Lyon, Cathy L Melvin, Sarah Norell, Martina Mueller, Michael B Potter, Rachel Richesson, Lynne D Richardson, Gery Ryan, Lauren Siewny, Marsha Treadwell, Leslie Zun, Janelle Armstrong-Brown, Lisa Cox, Paula Tanabe, Lingzi Luo, Allison A King, Yvonne Carroll, Ana A Baumann, Donald Brambilla, Christopher R Carpenter, Joseph Colla, Robert W Gibson, Siera Gollan, Greg Hall, Lisa Klesges, Abdullah Kutlar, Matthew Lyon, Cathy L Melvin, Sarah Norell, Martina Mueller, Michael B Potter, Rachel Richesson, Lynne D Richardson, Gery Ryan, Lauren Siewny, Marsha Treadwell, Leslie Zun, Janelle Armstrong-Brown, Lisa Cox, Paula Tanabe

Abstract

Background: Individuals living with sickle cell disease often require aggressive treatment of pain associated with vaso-occlusive episodes in the emergency department. Frequently, pain relief is poor. The 2014 National Heart, Lung, and Blood Institute evidence-based guidelines recommended an individualized treatment and monitoring protocol to improve pain management of vaso-occlusive episodes.

Objective: This study will implement an electronic health record-embedded individualized pain plan with provider and patient access in the emergency departments of 8 US academic centers to improve pain treatment for adult patients with sickle cell disease. This study will assess the overall effects of electronic health record-embedded individualized pain plans on improving patient and provider outcomes associated with pain treatment in the emergency department setting and explore barriers and facilitators to the implementation process.

Methods: A preimplementation and postimplementation study is being conducted by all 8 sites that are members of the National Heart, Lung, and Blood Institute-funded Sickle Cell Disease Implementation Consortium. Adults with sickle cell disease aged 18 to 45 years who had a visit to a participating emergency department for vaso-occlusive episodes within 90 days prior to enrollment will be eligible for inclusion. Patients will be enrolled in the clinic or remotely. The target analytical sample size of this study is 160 patient participants (20 per site) who have had an emergency department visit for vaso-occlusive episode treatment at participating emergency departments during the study period. Each site is expected to enroll approximately 40 participants to reach the analytical sample size. The electronic health record-embedded individualized pain plans will be written by the patient's sickle cell disease provider, and sites will work with the local informatics team to identify the best method to build the electronic health record-embedded individualized pain plan with patient and provider access. Each site will adopt required patient and provider implementation strategies and can choose to adopt optional strategies to improve the uptake and sustainability of the intervention. The study is informed by the Technology Acceptance Model 2 and the Reach, Effectiveness, Adoption, Implementation, and Maintenance framework. Provider and patient baseline survey, follow-up survey within 96 hours of an emergency department vaso-occlusive episode visit, and selected qualitative interviews within 2 weeks of an emergency department visit will be performed to assess the primary outcome, patient-perceived quality of emergency department pain treatment, and additional implementation and intervention outcomes. Electronic health record data will be used to analyze individualized pain plan adherence and additional secondary outcomes, such as hospital admission and readmission rates.

Results: The study is currently enrolling study participants. The active implementation period is 18 months.

Conclusions: This study proposes a structured, framework-informed approach to implement electronic health record-embedded individualized pain plans with both patient and provider access in routine emergency department practice. The results of the study will inform the implementation of electronic health record-embedded individualized pain plans at a larger scale outside of Sickle Cell Disease Implementation Consortium centers.

Trial registration: ClinicalTrials.gov NCT04584528; https://ichgcp.net/clinical-trials-registry/NCT04584528.

International registered report identifier (irrid): DERR1-10.2196/24818.

Keywords: RE-AIM; digital medicine; electronic health record; emergency department care; health innovation; implementation science; pain treatment; patient portal; sickle cell disease.

Conflict of interest statement

Conflicts of Interest: PT has received funding from the National Heart, Lung, and Blood Institute and is a consultant for CSL Behring LLC.

©Lingzi Luo, Allison A King, Yvonne Carroll, Ana A Baumann, Donald Brambilla, Christopher R Carpenter, Joseph Colla, Robert W Gibson, Siera Gollan, Greg Hall, Lisa Klesges, Abdullah Kutlar, Matthew Lyon, Cathy L Melvin, Sarah Norell, Martina Mueller, Michael B Potter, Rachel Richesson, Lynne D Richardson, Gery Ryan, Lauren Siewny, Marsha Treadwell, Leslie Zun, Janelle Armstrong-Brown, Lisa Cox, Paula Tanabe. Originally published in JMIR Research Protocols (http://www.researchprotocols.org), 16.04.2021.

Figures

Figure 1
Figure 1
An example of an E-IPP emergency department provider interface (Washington University). E-IPP: electronic health record–embedded individualized pain plan.
Figure 2
Figure 2
An example of an E-IPP patient portal (Washington University). E-IPP: electronic health record–embedded individualized pain plan.
Figure 3
Figure 3
Simplified Technology Acceptance Model 2.
Figure 4
Figure 4
Study flow chart. ED: emergency department; EHR: electronic health record; VOE: vaso-occlusive episode.

References

    1. Sickle cell disease: data and statistics. US Centers for Disease Control and Prevention. 2020. Dec 16, [2021-01-20]. .
    1. Scott RB. Health care priority and sickle cell anemia. JAMA. 1970 Oct 26;214(4):731–4.
    1. Quinn CT, Rogers ZR, McCavit TL, Buchanan GR. Improved survival of children and adolescents with sickle cell disease. Blood. 2010 Apr 29;115(17):3447–52. doi: 10.1182/blood-2009-07-233700.
    1. Payne AB, Mehal JM, Chapman C, Haberling DL. Mortality trends and causes of death in persons with sickle cell disease in the united states, 1979-2014. Blood. 2017;(Supplement 1):865.
    1. Ware RE, de Montalembert M, Tshilolo L, Abboud MR. Sickle cell disease. Lancet. 2017 Jul 15;390(10091):311–323. doi: 10.1016/S0140-6736(17)30193-9.
    1. Evensen CT, Treadwell MJ, Keller S, Levine R, Hassell KL, Werner EM, Smith WR. Quality of care in sickle cell disease: cross-sectional study and development of a measure for adults reporting on ambulatory and emergency department care. Medicine (Baltimore) 2016 Aug;95(35):e4528. doi: 10.1097/MD.0000000000004528. doi: 10.1097/MD.0000000000004528.
    1. Kavanagh PL, Hirshon JM. EDSC3: working to improve emergency department care of individuals with sickle cell disease. Ann Emerg Med. 2020 Sep;76(3S):S80–S82. doi: 10.1016/j.annemergmed.2020.08.016.
    1. Yawn BP, Buchanan GR, Afenyi-Annan AN, Ballas SK, Hassell KL, James AH, Jordan L, Lanzkron SM, Lottenberg R, Savage WJ, Tanabe PJ, Ware RE, Murad MH, Goldsmith JC, Ortiz E, Fulwood R, Horton A, John-Sowah J. Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members. JAMA. 2014 Sep 10;312(10):1033–48. doi: 10.1001/jama.2014.10517.
    1. Krishnamurti L, Smith-Packard B, Gupta A, Campbell M, Gunawardena S, Saladino R. Impact of individualized pain plan on the emergency management of children with sickle cell disease. Pediatr Blood Cancer. 2014 Oct;61(10):1747–53. doi: 10.1002/pbc.25024.
    1. Schefft MR, Swaffar C, Newlin J, Noda C, Sisler I. A novel approach to reducing admissions for children with sickle cell disease in pain crisis through individualization and standardization in the emergency department. Pediatr Blood Cancer. 2018 Oct;65(10):e27274. doi: 10.1002/pbc.27274.
    1. Kato-Lin Y, Krishnamurti L, Padman R, Seltman HJ. Does e-pain plan improve management of sickle cell disease associated vaso-occlusive pain crisis? a mixed methods evaluation. Int J Med Inform. 2014 Nov;83(11):814–24. doi: 10.1016/j.ijmedinf.2014.08.003.
    1. Tanabe P, Silva S, Bosworth HB, Crawford R, Paice JA, Richardson LD, Miller CN, Glassberg J. A randomized controlled trial comparing two vaso-occlusive episode (VOE) protocols in sickle cell disease (SCD) Am J Hematol. 2018 Feb;93(2):159–168. doi: 10.1002/ajh.24948. doi: 10.1002/ajh.24948.
    1. Della-Moretta S, Delatore L, Purcell M, Huang Y, Heinlein M, Adkins E, Desai P. The effect of use of individualized pain plans in sickle cell patients presenting to the emergency department. Ann Emerg Med. 2020 Sep;76(3S):S21–S27. doi: 10.1016/j.annemergmed.2020.08.008.
    1. Henry J, Pylypchuk T, Searcy T, Patel V. Adoption of electronic health record systems among US non-federal acute care hospitals: 2008–2015. ONC Data Brief 35. Office of the National Coordinator for Health Information Technology. 2016. May, [2021-02-05]. .
    1. Lobb R, Colditz GA. Implementation science and its application to population health. Annu Rev Public Health. 2013;34:235–51. doi: 10.1146/annurev-publhealth-031912-114444.
    1. DiMartino LD, Baumann AA, Hsu LL, Kanter J, Gordeuk VR, Glassberg J, Treadwell MJ, Melvin CL, Telfair J, Klesges LM, King A, Wun T, Shah N, Gibson RW, Hankins JS, Sickle Cell Disease Implementation Consortium The sickle cell disease implementation consortium: translating evidence-based guidelines into practice for sickle cell disease. Am J Hematol. 2018 Dec;93(12):E391–E395. doi: 10.1002/ajh.25282.
    1. Kanter J, Gibson R, Lawrence RH, Smeltzer MP, Pugh NL, Glassberg J, Masese RV, King AA, Calhoun C, Hankins JS, Treadwell M. Perceptions of US adolescents and adults with sickle cell disease on their quality of care. JAMA Netw Open. 2020 May 01;3(5):e206016. doi: 10.1001/jamanetworkopen.2020.6016.
    1. Glassberg JA. Improving emergency department-based care of sickle cell pain. Hematology Am Soc Hematol Educ Program. 2017 Dec 08;2017(1):412–417. doi: 10.1182/asheducation-2017.1.412.
    1. Jenerette CM, Pierre-Louis BJ, Matthie N, Girardeau Y. Nurses' attitudes toward patients with sickle cell disease: a worksite comparison. Pain Manag Nurs. 2015 Jun;16(3):173–81. doi: 10.1016/j.pmn.2014.06.007.
    1. Stewart KA, Parshad-Asnani M, Wonkam A, Bollinger J, Ngo Bitoungui V, Wonkam-Tingang E, Powell J, Desronvil K, Benson KRK, Clark A, Katz M, Martin B, Peterseim C, Williams C, Young N, Shah N, Tanabe P, Babyak M, Royal CDM. “Pain is subjective”: a mixed-method study of provider attitudes and practices regarding pain management in sickle cell disease across three countries. J Pain Symptom Manage. 2020 Sep 01; doi: 10.1016/j.jpainsymman.2020.08.029.
    1. Abdallah K, Buscetta A, Cooper K, Byeon J, Crouch A, Pink S, Minniti C, Bonham VL. Emergency department utilization for patients living with sickle cell disease: psychosocial predictors of health care behaviors. Ann Emerg Med. 2020 Sep;76(3):S56–S63. doi: 10.1016/j.annemergmed.2020.08.018.
    1. Haywood C, Lanzkron S, Hughes MT, Brown R, Massa M, Ratanawongsa N, Beach MC. A video-intervention to improve clinician attitudes toward patients with sickle cell disease: the results of a randomized experiment. J Gen Intern Med. 2011 May;26(5):518–23. doi: 10.1007/s11606-010-1605-5.
    1. Linton EA, Goodin DA, Hankins JS, Kanter J, Preiss L, Simon J, Souffront K, Tanabe P, Gibson R, Hsu LL, King A, Richardsona LD, Glassberg JA, Sickle Cell Disease Implementation Consortium A survey-based needs assessment of barriers to optimal sickle cell disease care in the emergency department. Ann Emerg Med. 2020 Sep;76(3S):S64–S72. doi: 10.1016/j.annemergmed.2020.08.013.
    1. Glasgow RE, Vogt TM, Boles SM. Evaluating the public health impact of health promotion interventions: the RE-AIM framework. Am J Public Health. 1999 Sep;89(9):1322–7. doi: 10.2105/ajph.89.9.1322.
    1. Tabak RG, Khoong EC, Chambers DA, Brownson RC. Bridging research and practice: models for dissemination and implementation research. Am J Prev Med. 2012 Sep;43(3):337–50. doi: 10.1016/j.amepre.2012.05.024.
    1. Glasgow RE, Harden SM, Gaglio B, Rabin B, Smith ML, Porter GC, Ory MG, Estabrooks PA. RE-AIM planning and evaluation framework: adapting to new science and practice with a 20-year review. Front Public Health. 2019;7:64. doi: 10.3389/fpubh.2019.00064. doi: 10.3389/fpubh.2019.00064.
    1. Holtrop JS, Rabin BA, Glasgow RE. Qualitative approaches to use of the RE-AIM framework: rationale and methods. BMC Health Serv Res. 2018 Mar 13;18(1):177. doi: 10.1186/s12913-018-2938-8.
    1. Venkatesh V, Davis FD. A theoretical extension of the technology acceptance model: four longitudinal field studies. Management Science. 2000 Feb;46(2):186–204. doi: 10.1287/mnsc.46.2.186.11926.
    1. Chan A, Tetzlaff JM, Altman DG, Laupacis A, Gøtzsche PC, Krleža-Jerić K, Hróbjartsson A, Mann H, Dickersin K, Berlin JA, Doré CJ, Parulekar WR, Summerskill WSM, Groves T, Schulz KF, Sox HC, Rockhold FW, Rennie D, Moher D. SPIRIT 2013 statement: defining standard protocol items for clinical trials. Ann Intern Med. 2013 Feb 05;158(3):200–7. doi: 10.7326/0003-4819-158-3-201302050-00583.
    1. Pinnock H, Barwick M, Carpenter CR, Eldridge S, Grandes G, Griffiths CJ, Rycroft-Malone J, Meissner P, Murray E, Patel A, Sheikh A, Taylor SJC, StaRI Group Standards for reporting implementation studies (StaRI) statement. BMJ. 2017 Mar 06;356:i6795. doi: 10.1136/bmj.i6795.
    1. Smith JD, Li DH, Rafferty MR. The implementation research logic model: a method for planning, executing, reporting, and synthesizing implementation projects. Implement Sci. 2020 Sep 25;15(1):84. doi: 10.1186/s13012-020-01041-8.
    1. Damschroder LJ, Aron DC, Keith RE, Kirsh SR, Alexander JA, Lowery JC. Fostering implementation of health services research findings into practice: a consolidated framework for advancing implementation science. Implement Sci. 2009 Aug 07;4:50. doi: 10.1186/1748-5908-4-50.
    1. The Sickle Cell Disease Implementation Consortium An introduction to the align study. Vimeo. [2021-01-19]. .
    1. Individualized care plans for acute sickle cell pain crises. Washington University School of Medicine Division of Emergency Medicine. [2021-01-19].
    1. Scaccia JP, Cook BS, Lamont A, Wandersman A, Castellow J, Katz J, Beidas RS. A practical implementation science heuristic for organizational readiness: R = MC. J Community Psychol. 2015 Apr;43(4):484–501. doi: 10.1002/jcop.21698.
    1. Kaji AH, Schriger D, Green S. Looking through the retrospectoscope: reducing bias in emergency medicine chart review studies. Ann Emerg Med. 2014 Sep;64(3):292–8. doi: 10.1016/j.annemergmed.2014.03.025.
    1. Gilbert EH, Lowenstein SR, Koziol-McLain J, Barta DC, Steiner J. Chart reviews in emergency medicine research: where are the methods? Ann Emerg Med. 1996 Mar;27(3):305–8. doi: 10.1016/s0196-0644(96)70264-0.
    1. Palinkas LA, Horwitz SM, Green CA, Wisdom JP, Duan N, Hoagwood K. Purposeful sampling for qualitative data collection and analysis in mixed method implementation research. Adm Policy Ment Health. 2015 Sep;42(5):533–44. doi: 10.1007/s10488-013-0528-y.
    1. Baumann AA, Belle SH, James A, King AA, Sickle Cell Disease Implementation Consortium Specifying sickle cell disease interventions: a study protocol of the Sickle Cell Disease Implementation Consortium (SCDIC) BMC Health Serv Res. 2018 Jun 27;18(1):500. doi: 10.1186/s12913-018-3297-1.
    1. Press A, McCullagh L, Khan S, Schachter A, Pardo S, McGinn T. Usability testing of a complex clinical decision support tool in the emergency department: lessons learned. JMIR Hum Factors. 2015 Sep 10;2(2):e14. doi: 10.2196/humanfactors.4537.
    1. Hoeksema LJ, Bazzy-Asaad A, Lomotan EA, Edmonds DE, Ramírez-Garnica G, Shiffman RN, Horwitz LI. Accuracy of a computerized clinical decision-support system for asthma assessment and management. J Am Med Inform Assoc. 2011 May 01;18(3):243–50. doi: 10.1136/amiajnl-2010-000063.
    1. Ray JM, Ahmed OM, Solad Y, Maleska M, Martel S, Jeffery MM, Platts-Mills TF, Hess EP, D'Onofrio G, Melnick ER. Computerized clinical decision support system for emergency department–initiated buprenorphine for opioid use disorder: user-centered design. JMIR Hum Factors. 2019 Feb 27;6(1):e13121. doi: 10.2196/13121.
    1. Mobile fact sheet. Pew Research Center. 2017. Jun 12, [2021-01-19].
    1. Badawy SM, Thompson AA, Liem RI. Technology access and smartphone app preferences for medication adherence in adolescents and young adults with sickle cell disease. Pediatr Blood Cancer. 2016 May;63(5):848–52. doi: 10.1002/pbc.25905.
    1. Estepp JH, Winter B, Johnson M, Smeltzer MP, Howard SC, Hankins JS. Improved hydroxyurea effect with the use of text messaging in children with sickle cell anemia. Pediatr Blood Cancer. 2014 Nov;61(11):2031–6. doi: 10.1002/pbc.25177.
    1. Tieu L, Schillinger D, Sarkar U, Hoskote M, Hahn KJ, Ratanawongsa N, Ralston JD, Lyles CR. Online patient websites for electronic health record access among vulnerable populations: portals to nowhere? J Am Med Inform Assoc. 2017 Apr 01;24(e1):e47–e54. doi: 10.1093/jamia/ocw098.
    1. Kooij L, Groen WG, van Harten WH. Barriers and facilitators affecting patient portal implementation from an organizational perspective: qualitative study. J Med Internet Res. 2018 May 11;20(5):e183. doi: 10.2196/jmir.8989.
    1. Foster B, Krasowski MD. The use of an electronic health record patient portal to access diagnostic test results by emergency patients at an academic medical center: retrospective study. J Med Internet Res. 2019 Jun 28;21(6):e13791. doi: 10.2196/13791.
    1. Goldzweig CL, Orshansky G, Paige NM, Towfigh AA, Haggstrom DA, Miake-Lye I, Beroes JM, Shekelle PG. Electronic patient portals: evidence on health outcomes, satisfaction, efficiency, and attitudes: a systematic review. Ann Intern Med. 2013 Nov 19;159(10):677. doi: 10.7326/0003-4819-159-10-201311190-00006.
    1. Kidwell KM, Peugh J, Westcott E, Nwankwo C, Britto MT, Quinn CT, Crosby LE. Acceptability and feasibility of a disease-specific patient portal in adolescents with sickle cell disease. J Pediatr Hematol Oncol. 2019 Oct;41(7):561–567. doi: 10.1097/MPH.0000000000001341.
    1. Handley MA, Lyles CR, McCulloch C, Cattamanchi A. Selecting and improving quasi-experimental designs in effectiveness and implementation research. Annu Rev Public Health. 2018 Apr 01;39:5–25. doi: 10.1146/annurev-publhealth-040617-014128.
    1. Palinkas LA, Aarons GA, Horwitz S, Chamberlain P, Hurlburt M, Landsverk J. Mixed method designs in implementation research. Adm Policy Ment Health. 2011 Jan;38(1):44–53. doi: 10.1007/s10488-010-0314-z.

Source: PubMed

3
Subscribe