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References

  • 1
    Holen JC, Hjermstad MJ, Loge JH, et al. Pain assessment tools: is the content appropriate for use in palliative care? J Pain Symptom Manage. 2006; 32: 567-580.
  • 2
    Clinical Practice Guidelines for Quality Palliative Care. Pittsburgh, PA: National Consensus Project for Quality Palliative Care; 2004.
  • 3
    A national framework and preferred practices for palliative and hospice care quality. Washington, DC: National Quality Forum; 2006.
  • 4
    Carolinas Center for Medical Excellence. Palliative care quality measurement project. Medicare quality improvement community (MedQIC-Hospice). 2008. Available at: www.medqic.org. Accessed on January 1, 2009.
  • 5
    Connor SR, Teno J, Spence C, Smith N. Family evaluation of hospice care: results from voluntary submission of data via website. J Pain Symptom Manage. 2005; 30: 9-17.
  • 6
    Earle CC, Neville BA, Landrum MB, et al. Evaluating claims-based indicators of the intensity of end-of-life cancer care. Int J Qual Health Care. 2005; 17: 505-509.
  • 7
    Etzioni S, Chodosh J, Ferrell BA, MacLean CH. Quality indicators for pain management in vulnerable elders. J Am Geriatr Soc. 2007;( 55 suppl 2): S403-S408.
  • 8
    Grunfeld E, Lethbridge L, Dewar R, et al. Towards using administrative databases to measure population-based indicators of quality of end-of-life care: testing the methodology. Palliat Med. 2006; 20: 769-777.
  • 9
    Jacobson JO, Neuss MN, McNiff KK, et al. Improvement in oncology practice performance through voluntary participation in the Quality Oncology Practice Initiative. J Clin Oncol. 2008; 26: 1893-1898.
  • 10
    Lorenz KA, Lynn J, Dy SM, et al. Quality measures for symptoms and advance care planning in cancer: a systematic review. J Clin Oncol. 2006; 24: 4933-4938.
  • 11
    Lorenz KA, Rosenfeld K, Wenger N. Quality indicators for palliative and end-of-life care in vulnerable elders. J Am Geriatr Soc. 2007; 55( suppl 2): S318-S326.
  • 12
    Miyashita M, Morita T, Tsuneto S, Sato K, Shima Y. The Japan Hospice and Palliative Care Evaluation Study (J-HOPE Study): study design and characteristics of participating institutions. Am J Hosp Palliat Care. 2008; 25: 223-232.
  • 13
    Mularski RA, Dy SM, Shugarman LR, et al. A systematic review of measures of end-of-life care and its outcomes. Health Serv Res. 2007; 42: 1848-1870.
  • 14
    Nelson JE, Mulkerin CM, Adams LL, Pronovost PJ. Improving comfort and communication in the ICU: a practical new tool for palliative care performance measurement and feedback. Qual Saf Health Care. 2006; 15: 264-271.
  • 15
    Twaddle ML, Maxwell TL, Cassel JB, et al. Palliative care benchmarks from academic medical centers. J Palliat Med. 2007; 10: 86-98.
  • 16
    National Quality Forum. National Voluntary Consensus Standards for Symptom Management and End-of-Life Care in Cancer Patients. Washington, DC. 2006. Available at: http://www.qualityforum.org. Accessed on January 1, 2009.
  • 17
    American Thoracic Society. Dyspnea. Mechanisms, assessment, and management: a consensus statement. Am J Respir Crit Care Med. 1999; 159: 321-340.
  • 18
    Dorman S, Byrne A, Edwards A. Which measurement scales should we use to measure breathlessness in palliative care? A systematic review. Palliat Med. 2007; 21: 177-191.
  • 19
    Institute of Medicine. Cancer care for the whole patient: meeting psychosocial health needs. 2008. Available at: http://www.iom.edu.
  • 20
    Haig KM, Sutton S, Whittington J. SBAR: a shared mental model for improving communication between clinicians. Jt Comm J Qual Patient Saf. 2006; 32: 167-175.
  • 21
    Sandlin D. Improving patient safety by implementing a standardized and consistent approach to hand-off communication. J Perianesth Nurs. 2007; 22: 289-292.