| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0027-9684(15)31069-5 |
| P698 | PubMed publication ID | 19860302 |
| P50 | author | Mary Catherine Beach | Q60533676 |
| Eric Bass | Q63368226 | ||
| P2093 | author name string | Jodi B Segal | |
| Carlton Haywood | |||
| Sophie Lanzkron | |||
| John J Strouse | |||
| Renee Wilson | |||
| Haeseong Park | |||
| Catherine Witkop | |||
| P2860 | cites work | Grading quality of evidence and strength of recommendations | Q24562409 |
| Health related quality of life in sickle cell patients: the PiSCES project | Q24810691 | ||
| Assessing the quality of reports of randomized clinical trials: is blinding necessary? | Q27860973 | ||
| Interventions for providers to promote a patient-centred approach in clinical consultations. | Q30329165 | ||
| Improving adherence with deferoxamine regimens for patients receiving chronic transfusion therapy | Q32022548 | ||
| Experiences of hospital care and treatment seeking for pain from sickle cell disease: qualitative study | Q33619896 | ||
| Parental health beliefs and compliance with prophylactic penicillin administration in children with sickle cell disease | Q34160875 | ||
| Cultural competence: a systematic review of health care provider educational interventions | Q35108154 | ||
| Provision of pneumococcal prophylaxis for publicly insured children with sickle cell disease | Q35207011 | ||
| Painful crises in sickle cell disease--patients' perspectives | Q35701064 | ||
| Physician knowledge and adherence to prescribing antibiotic prophylaxis for sickle cell disease | Q35776691 | ||
| Methodological rigour within a qualitative framework | Q35925758 | ||
| Evaluation of fast track admission policy for children with sickle cell crises: questionnaire survey of parents' preferences | Q36246290 | ||
| Hospitalization rates and costs of care of patients with sickle-cell anemia in the state of Maryland in the era of hydroxyurea. | Q36573473 | ||
| Trying to improve compliance with prophylactic penicillin therapy in children with sickle cell disease | Q38502419 | ||
| Compliance with penicillin prophylaxis in patients with sickle cell disease | Q39463978 | ||
| The role of social support in compliance and other health behaviors for African Americans with chronic illnesses | Q39493462 | ||
| Socioeconomic distress and health status: the urban-rural dichotomy of services utilization for people with sickle cell disorder in North Carolina | Q39543164 | ||
| Rural/urban differences in access to and utilization of services among people in Alabama with sickle cell disease | Q39642809 | ||
| Optimism predicting daily pain medication use in adolescents with sickle cell disease. | Q40235450 | ||
| Therapy preference and decision-making among patients with severe sickle cell anemia and their families | Q40321280 | ||
| Barriers to adherence of deferoxamine usage in sickle cell disease | Q42642783 | ||
| Paradigms and politics: shaping health care access for sickle cell patients through the discursive regimes of biomedicine. | Q45978285 | ||
| Using quality improvement strategies to enhance pediatric pain assessment | Q46093137 | ||
| Does race influence the provision of care to persons with sickle cell disease? Perceptions of multidisciplinary providers | Q46334785 | ||
| Hydroxyurea therapy for sickle cell disease in community-based practices: a survey of Florida and North Carolina hematologists/oncologists | Q46521677 | ||
| Meeting the challenge of managing vaso-occlusive crisis | Q47301409 | ||
| How much do sample characteristics affect the effect size? An investigation of studies testing the treatment effects for social phobia | Q47419467 | ||
| The management of sickle cell crisis pain as experienced by patients and their carers. | Q51135262 | ||
| Does a clinical pathway improve the quality of care for sickle cell anemia? | Q51677220 | ||
| Functions of an adult sickle cell group: education, task orientation, and support. | Q52038196 | ||
| Impact of children's sickle cell history on nurse and physician ratings of pain and medication decisions | Q52229906 | ||
| Sickle cell-related pain: perceptions of medical practitioners. | Q52275377 | ||
| Nurses' attitudes and practices in sickle cell pain management. | Q52280388 | ||
| Mortality in sickle cell disease. Life expectancy and risk factors for early death. | Q55065788 | ||
| Treating sickle cell pain like cancer pain | Q67747348 | ||
| Evaluation of qualitative research | Q73042454 | ||
| Does blinding of readers affect the results of meta-analyses? University of Pennsylvania Meta-analysis Blinding Study Group | Q73570669 | ||
| Parent factors and adolescent sickle cell disease: associations with patterns of health service use | Q74269003 | ||
| Sickle cell mutual assistance groups and the health services delivery system | Q74801850 | ||
| A natural history study of adolescents and young adults with sickle cell disease as they transfer to adult care: a need for case management services | Q77759017 | ||
| Pain management in sickle cell disease | Q79439264 | ||
| Structured telephone-based outreach using nonmedical personnel can improve adherence to comprehensive care in families of children with sickle cell disease | Q83300475 | ||
| P433 | issue | 10 | |
| P921 | main subject | sickle-cell disease | Q185034 |
| systematic review | Q1504425 | ||
| P304 | page(s) | 1022-1033 | |
| P577 | publication date | 2009-10-01 | |
| P1433 | published in | Journal of the National Medical Association | Q15752322 |
| P1476 | title | A systematic review of barriers and interventions to improve appropriate use of therapies for sickle cell disease | |
| P478 | volume | 101 |
| Q36792555 | A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell disease |
| Q30499650 | A video-intervention to improve clinician attitudes toward patients with sickle cell disease: the results of a randomized experiment |
| Q27318644 | Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research |
| Q33972260 | An unequal burden: poor patient-provider communication and sickle cell disease |
| Q35510092 | Attitudes toward patients with sickle cell disease in a multicenter sample of emergency department providers |
| Q64064319 | Barriers and facilitators to care for individuals with sickle cell disease in central North Carolina: The emergency department providers' perspective |
| Q88916011 | Barriers to Care for Persons With Sickle Cell Disease: The Case Manager's Opportunity to Improve Patient Outcomes |
| Q37093332 | Care seeking for pain in young adults with sickle cell disease. |
| Q50531951 | Coming of age with sickle cell disease and the role of patient as teacher. |
| Q91681227 | Comparative Effectiveness of a Web-Based Patient Decision Aid for Therapeutic Options for Sickle Cell Disease: Randomized Controlled Trial |
| Q44405893 | Cost-effectiveness of adenotonsillectomy in reducing obstructive sleep apnea, cerebrovascular ischemia, vaso-occlusive pain, and ACS episodes in pediatric sickle cell disease |
| Q43004271 | Development of interactive algorithm for clinical management of acute events related to sickle cell disease in emergency department. |
| Q41339681 | Disrespectful care in the treatment of sickle cell disease requires more than ethics consultation. |
| Q34285113 | Do difficulties in swallowing medication impede the use of hydroxyurea in children? |
| Q37238359 | Emergency provider analgesic practices and attitudes toward patients with sickle cell disease |
| Q38164192 | Emerging science of hydroxyurea therapy for pediatric sickle cell disease |
| Q30489282 | Evaluation of a Sickle Cell Disease Educational Website for Emergency Providers. |
| Q35599915 | Examining the characteristics and beliefs of hydroxyurea users and nonusers among adults with sickle cell disease. |
| Q33915407 | Hospital self-discharge among adults with sickle-cell disease (SCD): associations with trust and interpersonal experiences with care |
| Q36777717 | Hydroxyurea down-regulates BCL11A, KLF-1 and MYB through miRNA-mediated actions to induce γ-globin expression: implications for new therapeutic approaches of sickle cell disease |
| Q37223344 | Hydroxyurea use in sickle cell disease: the battle with low prescription rates, poor patient compliance and fears of toxicities |
| Q35537160 | Impact of a dedicated infusion clinic for acute management of adults with sickle cell pain crisis |
| Q47197206 | Improving Emergency Department-Based Care of Sickle Cell Pain. |
| Q36669645 | Improving Emergency Providers' Attitudes Toward Sickle Cell Patients in Pain |
| Q37305389 | Interventions for improving adherence to iron chelation therapy in people with sickle cell disease or thalassaemia |
| Q56389520 | Interventions for improving adherence to iron chelation therapy in people with sickle cell disease or thalassaemia |
| Q24197536 | Interventions to improve safe and effective medicines use by consumers: an overview of systematic reviews |
| Q92268179 | Management of Chronic Pain in Adults Living With Sickle Cell Disease in the Era of the Opioid Epidemic: A Qualitative Study |
| Q42531546 | Multiple Levels of Suffering: Discrimination in Health-Care Settings is Associated With Enhanced Laboratory Pain Sensitivity in Sickle Cell Disease |
| Q34570608 | Patient reports of health outcome for adults living with sickle cell disease: development and testing of the ASCQ-Me item banks |
| Q39011830 | Patient-provider communication about sexual concerns in cancer: a systematic review |
| Q34345527 | Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease |
| Q34566914 | Perceived discrimination, patient trust, and adherence to medical recommendations among persons with sickle cell disease |
| Q35561913 | Perceived injustice predicts stress and pain in adults with sickle cell disease |
| Q35619548 | Problematic hospital experiences among adult patients with sickle cell disease |
| Q37818015 | Psychosocial treatments in pain management of sickle cell disease. |
| Q37226191 | Quality of care in sickle cell disease: Cross-sectional study and development of a measure for adults reporting on ambulatory and emergency department care |
| Q35601509 | 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 |
| Q24194958 | Taking Medicines Safely and Effectively |
| Q91716403 | Targeted Hydroxyurea Education after an Emergency Department Visit Increases Hydroxyurea Use in Children with Sickle Cell Anemia |
| Q52865405 | The Association of Clinician Characteristics with their Attitudes Toward Patients with Sickle Cell Disease: Secondary Analyses of a Randomized Controlled Trial. |
| Q36717774 | The impact of race and disease on sickle cell patient wait times in the emergency department |
| Q37624297 | Transition from pediatric to adult care in sickle cell disease: Establishing evidence‐based practice and directions for research |
| Q37244255 | Voices of Adults Living with Sickle Cell Disease Pain |
| Q36888266 | Young Adult Perspectives on a Successful Transition from Pediatric to Adult Care in Sickle Cell Disease |
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