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Pain — Hospice Care Nursing Care Plan (NCP)

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HC-AcutePainNURSING DIAGNOSIS: Pain, acute/chronic

May be related to

  • Injuring agents (biological, chemical, physical, psychological)
  • Chronic physical disability

Possibly evidenced by

  • Verbal/coded report; preoccupation with pain
  • Changes in appetite/eating, weight; sleep patterns; altered ability to continue desired activities; fatigue
  • Guarded/protective behavior; distraction behavior (pacing/repetitive activities, reduced interaction with others)
  • Facial mask; expressive behavior (restlessness, moaning, crying, irritability); self-focusing; narrowed focus (altered time perception, impaired thought process)
  • Alteration in muscle tone (varies from flaccid to rigid)
  • Autonomic responses (diaphoresis, changes in BP, respiration, pulse); sympathetic mediated responses (temperature, cold, changes of body position, hypersensitivity)

Desired Patient Outcomes:

  • Report pain is relieved/controlled.
  • Verbalize methods that provide relief.
  • Follow prescribed pharmacological regimen.
  • Demonstrate use of relaxation skills and diversional activities as indicated.

Desired Family Outcomes: 

  • Cooperate in pain management program.

Pain — Hospice Care Nursing Care Plan (NCP): Nursing Interventions & Rationale

Nursing InterventionsRationale
 Perform a comprehensive pain evaluation, including location, characteristics, onset/duration, frequency, quality, severity (e.g., 0–10 scale), and precipitating/aggravating factors. Note cultural issues impacting reporting and expression of pain. Determine patient’s acceptable level of pain. Provides baseline information from which a realistic plan can be developed, keeping in mind that verbal/behavioral cues may have little direct relationship to the degree of pain perceived. Note: Often patient does not feel the need to be completely pain-free but is able to be more functional when pain is at lower level on the pain scale.
 Determine possible pathophysiological/psychological causes of pain Pain is associated with many factors that may be interactive and increase the degree of pain experienced.
 Assess patient’s perception of pain, along with behavioral and psychological responses. Determine patient’s attitude toward/use of pain medications and locus of control (internal/external). Helps identify patient’s needs and pain control methods found to be helpful or not helpful in the past. Note:Individuals with external locus of control may take little or no responsibility for pain management.
 Encourage patient/family to express feelings/concerns about narcotic use. Inaccurate information regarding drug use/fear of addiction or oversedation may impair pain control efforts.
 Verify current and past analgesic/narcotic drug use (including alcohol). May provide insight into what has/has not worked in the past or may impact therapy plan.
 Assess degree of personal adjustment to diagnosis, such as anger, irritability, withdrawal, acceptance. These factors are variable and often affect the perception of pain/ability to cope and need for pain management.
 Discuss with SO(s) ways in which they can assist patient and reduce precipitating factors. Promotes involvement in care and belief that there are things they can do to help.
 Identify specific signs/symptoms and changes in pain requiring notification of healthcare provider/medical intervention. Unrelieved pain may be associated with progression of terminal disease process, or be associated with complications that require medical management.
 Involve caregivers in identifying effective comfort measures for patient, e.g., use of nonacidic fluids, oral swabs/lip salve, skin/perineal care, enema. Instruct in use of oxygen/suction equipment as appropriate. Managing troubling symptoms such as nausea, dry mouth, dyspnea, constipation can reduce patient’s suffering and family anxiety, improving quality of life and allowing patient/family to focus on other issues.
 Demonstrate/encourage use of relaxation techniques, e.g., guided imagery, tapes/music, meditation. May reduce need for/can supplement analgesic therapy, especially during periods when patient desires to minimize sedative effects of medication.
Monitor for/discuss possibility of changes in mental status, e.g., agitation, confusion, restlessness.Although causes of deterioration are numerous in terminal stages, early recognition and management of the psychological component is an integral part of pain management.
Establish pain management plan with patient, family, and healthcare provider, including options for management of breakthrough pain.Inadequate pain management remains one of the most significant deficiencies in the care of the dying patient. A plan developed in advance increases patient’s level of trust that comfort will be maintained, reducing anxiety.
Schedule/administer analgesics as indicated to maximal dosage. Notify physician if regimen is inadequate to meet pain control goal.Helps maintain “acceptable” level of pain. Modifications of drug dosage/combinations may be required.
 Instruct patient, family/caregiver in use of IV pump (PCA) for pain control. When patient controls dosage and administration of medication, pain relief is enhanced and quality of life improved.

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