296 related articles for article (PubMed ID: 24300219)
1. Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.
Treadwell MJ; Hassell K; Levine R; Keller S
Clin J Pain; 2014 Oct; 30(10):902-14. PubMed ID: 24300219
[TBL] [Abstract][Full Text] [Related]
2. Sensitivity of alternative measures of functioning and wellbeing for adults with sickle cell disease: comparison of PROMIS® to ASCQ-Me℠.
Keller S; Yang M; Treadwell MJ; Hassell KL
Health Qual Life Outcomes; 2017 Jun; 15(1):117. PubMed ID: 28577358
[TBL] [Abstract][Full Text] [Related]
3. Patient reports of health outcome for adults living with sickle cell disease: development and testing of the ASCQ-Me item banks.
Keller SD; Yang M; Treadwell MJ; Werner EM; Hassell KL
Health Qual Life Outcomes; 2014 Aug; 12():125. PubMed ID: 25146160
[TBL] [Abstract][Full Text] [Related]
4. Psychometric analysis of the adult sickle cell quality of life measurement information system (ACSQ-Me) in a UK population.
Cooper O; McBain H; Tangayi S; Telfer P; Tsitsikas D; Yardumian A; Mulligan K
Health Qual Life Outcomes; 2019 Apr; 17(1):74. PubMed ID: 31036017
[TBL] [Abstract][Full Text] [Related]
5. Patient-reported outcomes in sickle cell disease and association with clinical and psychosocial factors: Report from the sickle cell disease implementation consortium.
Knisely MR; Pugh N; Kroner B; Masese R; Gordeuk V; King AA; Smith SM; Gurney JG; Adams R; Wun T; Snyder A; Glassberg J; Shah N; Treadwell M;
Am J Hematol; 2020 Sep; 95(9):1066-1074. PubMed ID: 32449965
[TBL] [Abstract][Full Text] [Related]
6. The relationship between frequency and severity of vaso-occlusive crises and health-related quality of life and work productivity in adults with sickle cell disease.
Rizio AA; Bhor M; Lin X; McCausland KL; White MK; Paulose J; Nandal S; Halloway RI; Bronté-Hall L
Qual Life Res; 2020 Jun; 29(6):1533-1547. PubMed ID: 31933113
[TBL] [Abstract][Full Text] [Related]
7. Health related quality of life in sickle cell patients: the PiSCES project.
McClish DK; Penberthy LT; Bovbjerg VE; Roberts JD; Aisiku IP; Levenson JL; Roseff SD; Smith WR
Health Qual Life Outcomes; 2005 Aug; 3():50. PubMed ID: 16129027
[TBL] [Abstract][Full Text] [Related]
8. Clinically meaningful interpretation of pediatric health-related quality of life in sickle cell disease.
Beverung LM; Varni JW; Panepinto JA
J Pediatr Hematol Oncol; 2015 Mar; 37(2):128-33. PubMed ID: 24942019
[TBL] [Abstract][Full Text] [Related]
9. Health-related quality of life and neuropathic pain in sickle cell disease in Jamaica.
Bartlett R; Ramsay Z; Ali A; Grant J; Rankine-Mullings A; Gordon-Strachan G; Asnani M
Disabil Health J; 2021 Oct; 14(4):101107. PubMed ID: 33867318
[TBL] [Abstract][Full Text] [Related]
10. Health-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium.
Dampier C; LeBeau P; Rhee S; Lieff S; Kesler K; Ballas S; Rogers Z; Wang W;
Am J Hematol; 2011 Feb; 86(2):203-5. PubMed ID: 21264908
[TBL] [Abstract][Full Text] [Related]
11. How sickle cell disease patients experience, understand and explain their pain: An Interpretative Phenomenological Analysis study.
Coleman B; Ellis-Caird H; McGowan J; Benjamin MJ
Br J Health Psychol; 2016 Feb; 21(1):190-203. PubMed ID: 26333530
[TBL] [Abstract][Full Text] [Related]
12. Development of the PedsQL™ Sickle Cell Disease Module items: qualitative methods.
Panepinto JA; Torres S; Varni JW
Qual Life Res; 2012 Mar; 21(2):341-57. PubMed ID: 21638090
[TBL] [Abstract][Full Text] [Related]
13. Emotional reactions to pain predict psychological distress in adult patients with Sickle Cell Disease (SCD).
Edwards CL; Killough A; Wood M; Doyle T; Feliu M; Barker CS; Uppal P; DeCastro L; Wellington C; Whitfield KE; O'Garo KG; Morgan K; Edwards Alesii LY; Byrd GS; McCabe M; Goli V; Keys A; Hill L; Collins-McNeil J; Trambadia J; Guinyard D; Muhammad M; McDonald P; Schmechel DE; Robinson E
Int J Psychiatry Med; 2014; 47(1):1-16. PubMed ID: 24956913
[TBL] [Abstract][Full Text] [Related]
14. A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease.
Taylor LE; Stotts NA; Humphreys J; Treadwell MJ; Miaskowski C
J Pain Symptom Manage; 2010 Sep; 40(3):416-35. PubMed ID: 20656451
[TBL] [Abstract][Full Text] [Related]
15. An evaluation of patient-reported outcomes in sickle cell disease within a conceptual model.
Treadwell MJ; Mushiana S; Badawy SM; Preiss L; King AA; Kroner B; Chen Y; Glassberg J; Gordeuk V; Shah N; Snyder A; Wun T;
Qual Life Res; 2022 Sep; 31(9):2681-2694. PubMed ID: 35445915
[TBL] [Abstract][Full Text] [Related]
16. 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).
Osunkwo I; Andemariam B; Minniti CP; Inusa BPD; El Rassi F; Francis-Gibson B; Nero A; Trimnell C; Abboud MR; Arlet JB; Colombatti R; de Montalembert M; Jain S; Jastaniah W; Nur E; Pita M; DeBonnett L; Ramscar N; Bailey T; Rajkovic-Hooley O; James J
Am J Hematol; 2021 Apr; 96(4):404-417. PubMed ID: 33264445
[TBL] [Abstract][Full Text] [Related]
17. Quality of life among adolescents with sickle cell disease: mediation of pain by internalizing symptoms and parenting stress.
Barakat LP; Patterson CA; Daniel LC; Dampier C
Health Qual Life Outcomes; 2008 Aug; 6():60. PubMed ID: 18691422
[TBL] [Abstract][Full Text] [Related]
18. Somatic symptom burden in adults with sickle cell disease predicts pain, depression, anxiety, health care utilization, and quality of life: the PiSCES project.
Sogutlu A; Levenson JL; McClish DK; Rosef SD; Smith WR
Psychosomatics; 2011; 52(3):272-9. PubMed ID: 21565599
[TBL] [Abstract][Full Text] [Related]
19. Descriptive analysis of sickle cell patients living in France: The PHEDRE cross-sectional study.
Gerardin M; Rousselet M; Couec ML; Masseau A; Guerlais M; Authier N; Deheul S; Roussin A; Micallef J; Djezzar S; ; Feuillet F; Jolliet P; Victorri-Vigneau C
PLoS One; 2021; 16(3):e0248649. PubMed ID: 33735176
[TBL] [Abstract][Full Text] [Related]
20. Quality of care in sickle cell disease: Cross-sectional study and development of a measure for adults reporting on ambulatory and emergency department care.
Evensen CT; Treadwell MJ; Keller S; Levine R; Hassell KL; Werner EM; Smith WR
Medicine (Baltimore); 2016 Aug; 95(35):e4528. PubMed ID: 27583862
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
