Patient-reported outcomes: descriptors of nociceptive and neuropathic pain and barriers to effective pain management in adult outpatients with sickle cell disease - Wikidata - awgldk - TriplyDB

Patient-reported outcomes: descriptors of nociceptive and neuropathic pain and barriers to effective pain management in adult outpatients with sickle cell disease

Patient-reported outcomes: descriptors of nociceptive and neuropathic pain and barriers to effective pain management in adult outpatients with sickle cell disease

http://www.wikidata.org/entity/Q36809000

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Inhaled nitric oxide for treating pain crises in people with sickle cell disease Pain and symptom management in palliative care and at end of life Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.CaMKIIα may modulate fentanyl-induced hyperalgesia via a CeLC-PAG-RVM-spinal cord descending facilitative pain pathway in rats Outpatient pain predicts subsequent one-year acute health care utilization among adults with sickle cell disease.Sickle cell disease: an opportunity for palliative care across the life span.Dopamine D3 receptor Ser9Gly and catechol-o-methyltransferase Val158Met polymorphisms and acute pain in sickle cell disease.The use of neuropathic pain drugs in children with sickle cell disease is associated with older age, female sex, and longer length of hospital stay.Neuropathic pain in patients with sickle cell disease.Dexmedetomidine ameliorates nocifensive behavior in humanized sickle cell mice.Perceived injustice predicts stress and pain in adults with sickle cell disease Safety and Utility of Quantitative Sensory Testing among Adults with Sickle Cell Disease: Indicators of Neuropathic Pain?Parents' management of children's pain at home after surgery Early insights into the neurobiology of pain in sickle cell disease: A systematic review of the literature.The influence of scapular depression on upper limb neurodynamic test responses.Comparative Analysis of Pain Behaviours in Humanized Mouse Models of Sickle Cell Anemia.USING LIVED EXPERIENCES OF ADULTS TO UNDERSTAND CHRONIC PAIN: SICKLE CELL DISEASE, AN EXEMPLAR.Satisfied or not satisfied: pain experiences of patients with sickle cell disease.Dexmedetomidine as an Adjuvant to Analgesic Strategy During Vaso-Occlusive Episodes in Adolescents with Sickle-Cell Disease.Patients with sickle cell disease have increased sensitivity to cold and heat.Neutrophils, platelets, and inflammatory pathways at the nexus of sickle cell disease pathophysiology.Creative partnerships for funding nursing research.Neurobiological mechanisms of pain in sickle cell disease.Toward understanding family-related characteristics of young adults with sickle-cell disease or sickle-cell trait in the USA Model for the First NIH-funded Center of Excellence in End-of-Life Research.Presence of neuropathic pain as an underlying mechanism for pain associated with cold weather in patients with sickle cell disease.Prevalence of pain-related single nucleotide polymorphisms in patients of African origin with sickle cell disease PKCδ-targeted intervention relieves chronic pain in a murine sickle cell disease model Pain measurement as part of primary healthcare of adult patients with sickle cell disease.Voices of Adults Living with Sickle Cell Disease Pain.Mechanism-driven phase I translational study of trifluoperazine in adults with sickle cell disease.Thinking beyond sickling to better understand pain in sickle cell disease.Pain quality descriptors in community-dwelling older adults with nonmalignant pain.Addressing challenges of clinical trials in acute pain: The Pain Management of Vaso-occlusive Crisis in Children and Young Adults with Sickle Cell Disease Study.Patient-reported neuropathic pain in adolescent and young adult cancer patients.IL1A rs1800587 associates with chronic noncrisis pain in sickle cell disease.Implementing the PAIN RelieveIt Randomized Controlled Trial in Hospice Care: Mechanisms for Success and Meeting PCORI Methodology Standards.Inhibition of CaMKIIα in the Central Nucleus of Amygdala Attenuates Fentanyl-Induced Hyperalgesia in Rats.Coping with Pain in the Face of Healthcare Injustice in Patients with Sickle Cell Disease.Does cold hypersensitivity increase with age in sickle cell disease?

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Patient-reported outcomes: descriptors of nociceptive and neuropathic pain and barriers to effective pain management in adult outpatients with sickle cell disease

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Journal of the National Medical Association

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Patient-reported outcomes: des ...... ients with sickle cell disease

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Debra Boyd-Seal

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Diana J Wilkie

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Harriet Wittert

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Marie L Suarez

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Robert Molokie

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Shiping Zong

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Yogen Saunthararajah

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Young Ok Kim

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Zaijie J Wang

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Zhongsheng Zhao

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P2860

The McGill Pain Questionnaire: major properties and scoring methods

Developing a computerized data collection and decision support system for cancer pain management.

The management of cancer pain.

Neuropathic pain: redefinition and a grading system for clinical and research purposes.

Daily assessment of pain in adults with sickle cell disease.

Computer and internet use among urban African Americans with type 2 diabetes.

Effects of coaching patients with lung cancer to report cancer pain.

Pain barriers: psychometrics of a 13-item questionnaire

Cognitive testing of PAINReportIt in adult African Americans with sickle cell disease.

A randomized trial of a representational intervention to decrease cancer pain (RIDcancerPain).

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18-27

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10.1016/S0027-9684(15)30471-5

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1

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102

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20158132

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sickle-cell disease

neuropathic pain

pain management

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3641147

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