Before, During and After The End : End of Life Care

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Transcription:

Before, During and After The End : End of Life Care Jeannie Meyer, MSN, RN, CCRN, CCNS, PCCN, ACHPN Clinical Nurse Specialist for Palliative Care With appreciation to Suzanne Graf, RN, CNS and Mary Hersh PhD, RN, FPCN, CHPN for sharing their materials.

The Beginning of the end The prognosis, the treatment options and the plan. Goals of care should be discussed with the physicians on the case prior to initiation of a discussion. How do we see this ending? (Just because we can, SHOULD we?) Beyond the hospital setting: discharge and rehab expectations. Resuscitation realities: If you ve got a ventilator, pressors, antiarrhythmics and artificial pacing, you re already coding the patient. At that point, no compressions, no defibrillation may be the only other options. It s hard to arrest in a hospital! Arrest = catastrophic event.

Resuscitation: the glamour and the myth On national television, 75% of cardiac arrest patients survive. Most have positive outcomes. Little discussion of the real aftermath of a resuscitation effort. Ventilators Medications Downward trajectory Survival to discharge Quality of Life after discharge

For every minute that an individual is in arrest (no respirations or pulse) the chance of meaningful survival decreases 10%*. Even among previously healthy patients, only 15% survive after a resuscitation to be discharged from the hospital. Cardiopulmonary resuscitation: the grim reality Many patients have less than a 2% chance of survival: Patients with pre existing chronic medical conditions. Those who do not live independently (such as nursing home patients or patients dependent on others for their care for medical reasons). Those with terminal illness. These statistics do not address the longterm survival or quality of life. *American Heart Association.

So why do it? The Original Intent of CPR For the reasonably healthy individual. Sudden, catastrophic event. Reversible condition (ex. Stroke that can be treated). Abnormal heart rhythm that can respond to electric shock and that has an underlying cause that can be treated.

In speaking to patients and their significant others Are you speaking to the person(s) who have the power to make the decision? If there is a Directive and a copy has not yet been provided, request it, and find out the gist of what it says. Avoiding the crazy daughter from Tuscaloosa. What have you been told about your own/your loved one s condition? The physician update can help ensure that everyone is told the same thing (even if they may not all hear the same thing ). Who is this person? Has he/she ever made any comments or expressed any wishes pertaining to the current situation? If he could speak to you now

Faith, belief system, culture Not our goals, their goals However: In cases where the healthcare practitioner believes that the patient s wishes are not being honored, best interests are not being respected, or in cases of known or suspected medical futility, get an Ethics consult! As a professional courtesy, the primary and critical care physician(s) should be notified prior to the initiation of an Ethics consult by another healthcare team member. Even patients and loved ones with no specific belief system have spiritual distress and existential suffering. Contact your chaplain to offer support. Be aware of concerns outside of the dying process that may be contributing to suffering (financial concerns, questions about child custody, etc.) Contact a Social Worker if needed. When in doubt, Don t Ask Just Call!

And once the decision has been made

Understanding death Death is holistic: Body.. Mind.. Spirit Signs and Symptoms can differ slightly depending on the type of death The usual road A gradual decline leading to unconsciousness then death The difficult road Complicated by distressing symptoms such as seizures, confusion, delirium, restlessness/pain Seen frequently in setting that limit a peaceful/calm environment (hospital, nursing homes, Long term Care, etc.). Nurses or care partners often are the first to notice when a patient is actively dying

Early stages Sensation/Perception Impaired perception Disorientation Decrease visual acuity Increased light sensitivity Dulled senses Hearing remains intact

Early stages Cardiopulmonary Increase respiratory and heart rate Cheyne stokes respirations or periods of apnea Difficulty clearing secretions Death rattle

Early Stages Renal Decreased urine output Incontinence Urinary retention Musculoskeletal Gradual loss of ability to move Starts in the legs May lead to immobility related pain and discomfort.

Late stages Sensation/Perception Unconscious/obtunded Loss of blink reflex Dry/irritated eyes Eyes remain half open Hearing may still remain intact

Late stages Cardio Pulmonary/Renal Heart rate may double then start to decrease Rhythm may become irregular, and strength minimizes Cool to touch, diaphoretic Mottling in extremities Signs of cyanosis Decreasing peripheral pulses followed by absence Drastic decrease in urine output indicates near death

First do no harm Misconceptions about End of Life Care Care is withdrawn or withheld Withdrawal of Life Prolonging Treatment/Life Support Euthanasia is performed Medications are given to alleviate symptoms Patients die more quickly There is no literature supporting the belief that patients die more quickly who receive aggressive end of life care. Can we get this over with? No. The patient is on his own journey. The patient is unresponsive, so there is no pain We evaluate for presumptive pain indicators Minimal or no documentation is needed for End of Life Patients Pain/agitation/dyspnea and other symptoms must be documented at least every 2 hours.

Support for the Dying Bereavement Packet (addresses concerns that may rise before, during and after the dying process). No One Dies Alone (NODA): a volunteer program to support the dying who have no one with them. Spiritual Care Integrative Therapies: music, pet therapy (Palliative Pups), Urban Zen

Pain Recognition at EOL Choosing the right pain scale Numeric/Faces ONLY use Faces if they can/will Point to the Face. Verbal Descriptors (a little, a great deal, or in the middle?) PAIN AD CPOT/Non cog Pain versus Anxiety Delirium 17 (Fink & Gates, 2006)

PAIN AD Tool Items 0 1 2 SCORE Breathing Independent of vocalization Negative vocalization Normal None Occasional labored breathing. Short period of hyperventilation Occasional moan or groan. Low level of speech with a negative or disapproving quality. Facial Expression Smiling or inexpressive Sad, frightened, frown. Body Language Relaxed Tense. Distressed pacing. Fidgeting. Consolibility No need to console Distracted or reassured by voice or touch. Noisy labored breathing. Long period of hyperventilation. Cheyne stokes respirations. Repeated troubled calling out. Loud moaning or groaning. Crying. Facial grimacing. Rigid. Fists clenched. Knees pulled up. Pulling or pushing away. Striking out. Unable to console, distract, or reassure. Total (Warden, Hurley, & Volicer, 2003) 18

CPOT (Gelinas, Harel, Fillion, Puntillo, & Johnston, 2009) 19

Why bolus versus titration? Bolus Max concentration IV = 15 minutes Sub Q = 30 minutes PO = 1 hour Titration The full effect of a continuous IV infusion (or basal rate) will not be felt until steady state is reached (about 10 20 hours) 20 (Chris Pietras, MD)

Morphine IV Bolus Versus 100% Continuous Infusion 90% Percent of maximum plasma concentration 80% 70% 60% 50% 40% 30% 20% bolus dose of 10mg continuous infusion of 1.25mg/hr 10% 0% 0 4 8 12 16 20 24 Time in hours (4 hours = 1 half life) 21 (Chris Pietras, MD)

What do doctors want RNs to know? RNs at the bedside know more Be confident in your assessments Ask the doctors for appropriate orders 22

References Dudgeon, D. (2016). Dyspnea, death rattle, and cough. In B. Ferrell & N. Coyle (Eds.), Textbook of palliative nursing. New York, NY: Oxford University Press. Englot, D.J., Chang, E.F., & Vecht, C.J. (2016). Epilepsy and brain tumors. Handbook of Clinical Neurology Palliative care at the endof life in glioma patients. Handbook of Clinical Neurology. In MS. Berger & M. Weller (Eds.) Gliomas (pp. 267 285). San Francisco, CA: Elsevier. Fink, R., & Gates, R. (2016). Pain assessment. In B. R. Ferrell & N. Coyle (Eds.), Textbook of palliative nursing (2nd ed., pp. 97 129). New York, NY: Oxford University Press. 23

References (continued) Gelinas, C., Harel, F., Fillion, L., Puntillo, K. A., & Johnston, C. C. (2009). Sensitivity and specificity of the critical care pain observation tool for the detection of pain in intubated adults after cardiac surgery. Journal of Pain and Symptom Management, 37(1), 58 67. Paice, J. A., & Fine, P. G. (2016). Pain at the end of life. In B. Ferrell & N. Coyle (Eds.), Textbook of palliative nursing. New York, NY: Oxford University Press. Warden, V., Hurley, A.C., & Volicer, V. (2003). Development and psychometric evaluation of the pain assessment in advanced dementia (PAINAD) scale. Journal of Medical Directors Association, 4(1), 9 15. 24