Authors

  1. Kelley, Carol G. PhD, RN

Article Content

To the Editor:

 

We read with interest the recent article by Koesel (March 2008) which discussed the positive outcomes of effective communication and symptom management by a palliative care advanced practice nurse (APN) for chronically critically ill (CCI) patients. While Ms Koesel raised several very important issues related to providing care to CCI patients at end of life, we have also noted in our work the very important role that the APN can play in providing communication and support for the caregivers of CCI patients. While the patient in Ms Koesel's article was cognitively intact, we have found that up to 40% of CCI patients are cognitively impaired during their hospital course,1 thus increasing the responsibilities placed upon their caregivers to not only provide support but also play an active role in decision making. We have found that the APN can play a significant role as an advocate for the patient and caregiver in addition to providing information and support.2 This role is particularly important as we (and others) have documented that the caregivers of CCI are at high risk for depression and burden, regardless of where the patient resides.1,3 Finally, Koesel identified that CCI patients and their caregivers are not prepared for poor outcomes and stressed the importance of end-of-life (EOL) care for these patients. We would also add to Ms Koesel's assessment the importance of EOL discussions with the caregivers of CCI patients as well. In a recent study that examined CCI caregiver satisfaction and preparation with EOL care, we found that caregivers identified the importance of being able to talk to the healthcare provider and discuss specific events leading to their loved one's death as key to their satisfaction and preparation with EOL care.4 Thus, while we agree with Ms Koesel that CCI patients benefit greatly from the palliative and EOL care services of an APN, we would also add that the caregivers of these patients benefit as much, if not more, from such a relationship.

 

Carol G. Kelley, PhD, RN

 

Assistant Professor

 

Frances Payne Bolton

 

School of Nursing

 

Case Western Reserve University

 

Cleveland, OH

 

Sara L. Douglas, PhD, RN

 

Associate Professor

 

Frances Payne Bolton

 

School of Nursing

 

Case Western Reserve University

 

Cleveland, OH

 

Barbara J. Daly, PhD, RN

 

Professor

 

Frances Payne Bolton

 

School of Nursing

 

Case Western Reserve University

 

Cleveland, OH

 

References

 

1. Douglas SL, Daly BJ, Kelley CG, O'Toole E, Montenegro H. Impact of a disease management program upon caregivers of long-term ventilator patients. Chest. 2005;128(6):3925-3936. [Context Link]

 

2. DM program cuts readmission days: nursing study focuses on at-risk patients. Dis Manag Advis. 2007;13(12):142-144. [Context Link]

 

3. Van Pelt DC, Milbrandt EB, Qin L, et al. Informal caregiver burden among survivors of prolonged mechanical ventilation. Am J Respir Crit Care Med. 2007;175(2):167-173. [Context Link]

 

4. Kelley CG, Daly BJ, Douglas SL, Standing T. Racial differences in perceptions held by caregivers of long-term ventilator patients at the end-of-life. Int J Palliat Nurs. 2007;13(1):30-38. [Context Link]