A systematic review of barriers and interventions to improve appropriate use of therapies for sickle cell disease.
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Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.Evaluation of a Sickle Cell Disease Educational Website for Emergency Providers.A video-intervention to improve clinician attitudes toward patients with sickle cell disease: the results of a randomized experimentHospital self-discharge among adults with sickle-cell disease (SCD): associations with trust and interpersonal experiences with care.An unequal burden: poor patient-provider communication and sickle cell disease.Do difficulties in swallowing medication impede the use of hydroxyurea in children?Perceived discrimination in health care is associated with a greater burden of pain in sickle cell diseasePerceived discrimination, patient trust, and adherence to medical recommendations among persons with sickle cell diseasePatient reports of health outcome for adults living with sickle cell disease: development and testing of the ASCQ-Me item banksAttitudes toward patients with sickle cell disease in a multicenter sample of emergency department providersImpact of a dedicated infusion clinic for acute management of adults with sickle cell pain crisisPerceived injustice predicts stress and pain in adults with sickle cell diseaseExamining the characteristics and beliefs of hydroxyurea users and nonusers among adults with sickle cell disease.Respect, trust, and the management of sickle cell disease pain in hospital: comparative analysis of concern-raising behaviors, preliminary model, and agenda for international collaborative research to inform practice.Problematic hospital experiences among adult patients with sickle cell diseaseImproving Emergency Providers' Attitudes Toward Sickle Cell Patients in PainThe impact of race and disease on sickle cell patient wait times in the emergency departmentHydroxyurea down-regulates BCL11A, KLF-1 and MYB through miRNA-mediated actions to induce γ-globin expression: implications for new therapeutic approaches of sickle cell diseaseA systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell diseaseYoung Adult Perspectives on a Successful Transition from Pediatric to Adult Care in Sickle Cell Disease.Care seeking for pain in young adults with sickle cell disease.Hydroxyurea use in sickle cell disease: the battle with low prescription rates, poor patient compliance and fears of toxicities.Quality of care in sickle cell disease: Cross-sectional study and development of a measure for adults reporting on ambulatory and emergency department careEmergency provider analgesic practices and attitudes toward patients with sickle cell diseaseVoices of Adults Living with Sickle Cell Disease Pain.Interventions for improving adherence to iron chelation therapy in people with sickle cell disease or thalassaemiaTransition from pediatric to adult care in sickle cell disease: establishing evidence-based practice and directions for research.Emerging science of hydroxyurea therapy for pediatric sickle cell disease.Patient-provider communication about sexual concerns in cancer: a systematic review.Disrespectful care in the treatment of sickle cell disease requires more than ethics consultation.Multiple Levels of Suffering: Discrimination in Health-Care Settings is Associated With Enhanced Laboratory Pain Sensitivity in Sickle Cell DiseaseDevelopment of interactive algorithm for clinical management of acute events related to sickle cell disease in emergency department.Interventions for improving adherence to iron chelation therapy in people with sickle cell disease or thalassaemia
P2860
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P2860
A systematic review of barriers and interventions to improve appropriate use of therapies for sickle cell disease.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on October 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A systematic review of barrier ...... apies for sickle cell disease.
@en
A systematic review of barrier ...... apies for sickle cell disease.
@nl
type
label
A systematic review of barrier ...... apies for sickle cell disease.
@en
A systematic review of barrier ...... apies for sickle cell disease.
@nl
prefLabel
A systematic review of barrier ...... apies for sickle cell disease.
@en
A systematic review of barrier ...... apies for sickle cell disease.
@nl
P2093
P1476
A systematic review of barrier ...... apies for sickle cell disease.
@en
P2093
Carlton Haywood
Catherine Witkop
Eric B Bass
Haeseong Park
Jodi B Segal
John J Strouse
Renee Wilson
Sophie Lanzkron
P304
P577
2009-10-01T00:00:00Z