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Fundamentals
문제

A 68-year-old patient with advanced dementia is admitted for pneumonia. The patient's daughter expresses frustration, saying, 'My mother keeps pulling out her IV line, and I feel helpless watching her.' Which nursing intervention would be most appropriate to address the daughter's psychosocial distress?

해설
Validating the daughter's feelings and offering collaborative problem-solving addresses her psychosocial distress effectively. Other options dismiss her concerns, focus solely on technical solutions, or offer false reassurance.
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심화 해설

Understanding the Psychosocial Distress in Dementia Caregiving

The daughter's statement reveals a dual-layer distress common among family caregivers of persons with dementia: frustration with a specific behavioral symptom (IV line removal) and a deeper sense of helplessness. Research consistently identifies that family caregivers experience disproportionately high rates of psychological distress and perceived burden [3]. The daughter's expression of helplessness is not merely a reaction to the IV line incident but reflects the broader emotional toll of witnessing a loved one's cognitive decline and inability to control the situation.

Evaluating the Nursing Interventions

The correct approach must address both the immediate safety concern and the caregiver's emotional state through a collaborative, empowering framework.

Option 1 offers a practical solution but prematurely jumps to problem-solving. While psychoeducation and behavioral management techniques are core components of evidence-based caregiver interventions like START (STrAtegies for RelaTives) [2], introducing them before acknowledging the emotional distress can invalidate the daughter's feelings. This approach risks making the caregiver feel unheard, as it prioritizes the patient's behavior over the caregiver's expressed emotional pain.

Option 2 uses a therapeutic communication technique of offering open-ended exploration. However, the phrase "it's common for family members to feel helpless" can be perceived as dismissive or normalizing in a way that shuts down further dialogue. It frames the distress as a routine occurrence rather than a unique, painful experience for this individual. The evidence supports interventions that foster meaning-making and social connection to mitigate caregiver anxiety and depression [1], which requires a more engaged and validating response than simple normalization.

Option 4 is dismissive and non-therapeutic. Telling a distressed family member "Don't worry" and to focus solely on their own well-being disregards their immediate emotional state, invalidates their caregiving role, and creates a barrier to communication. This approach contradicts the principles of family-centered care and does not align with any supportive intervention model.

Option 3 is the most appropriate intervention. The statement "I can see how distressing this is for you" provides immediate validation of the daughter's emotional experience, which is a foundational step in building a therapeutic alliance. The phrase "Let's work together" directly counters the daughter's stated feeling of helplessness by inviting her into a collaborative partnership. This approach mirrors the core philosophy of effective caregiver interventions. For instance, the START intervention is designed to be delivered in a structured, collaborative manner to improve caregiver mood and quality of life [2]. Similarly, a storytelling intervention like Caregiver Speaks aims to support caregivers by facilitating meaning-making within a supportive context, implicitly validating their experience [1]. By framing the goal as keeping the mother "safe and comfortable," the nurse acknowledges the daughter's underlying motivation of love and concern, transforming the interaction from a technical problem (IV removal) into a shared mission of compassionate care. This collaborative, validating approach is a key element of psychoeducational interventions that have been shown to be effective for family caregivers across diverse cultural settings .
References (research sources)
  • [1]
    Caregiver speaks: a randomized controlled trial of a storytelling intervention for hospice family caregivers of persons with dementia.RCT/clinical trialRolbiecki AJ, Rolbiecki AJ, Pitzer K, Benson JJ, Washington KT, Teti M, Kruse RL, Mehr DR, Smith J, Oliver D. (2026) · DOI: 10.1093/geront/gnag117
  • [2]
    Cultural and linguistic adaptation and delivery of START (STrAtegies for RelaTives) for caregivers of people with dementia in India: a mixed method study.Research articleVenkatesan S, Livingston G, Vaitheswaran S, Nagarajan G, Srinivasan N, Ramanujam V, Sargunan S, Fisher E, Rapaport P, Spector A. (2026) · DOI: 10.1080/13607863.2026.2631447
  • [3]
    A feasibility study on the efficacy of a VR-based mindfulness intervention for dementia caregivers in the home environment: A pilot randomized control trial protocol.RCT/clinical trialWang Q, Yu D, Wong G, Zhang D, Knapp M, Amoah PA, Li J, Shi C. (2026) · DOI: 10.1371/journal.pone.0347988

임상 시나리오

Clinical Practice Guide: Supporting a Distressed Dementia Caregiver
Situation

A 68-year-old patient with advanced dementia is admitted for pneumonia. Her daughter, the primary caregiver, expresses frustration and helplessness over her mother repeatedly pulling out the IV line.

Nursing Focus

The priority is to address the daughter's psychosocial distress using a dual approach that validates her emotional state and collaboratively engages her in the care plan. This reduces caregiver burden and improves patient safety.

Key Actions
  • Acknowledge and Validate: Start by naming the emotion you observe. Use phrases like, "I can see how distressing this is for you." This builds trust and makes the caregiver feel heard before any problem-solving begins.
  • Collaborate, Don't Dictate: Frame the next steps as a partnership. Use "we" language, such as "Let's work together to find ways to keep your mother safe and comfortable." This empowers the caregiver and respects their unique knowledge of the patient.
  • Assess Coping and Provide Resources: After establishing rapport, gently explore the caregiver's own coping mechanisms and support system. Offer referrals to social work, spiritual care, or community resources like the Alzheimer's Association for ongoing support.
Communication Pitfalls to Avoid
  • Premature Reassurance: Avoid statements like "Don't worry" or "We'll handle it." This dismisses the caregiver's valid concerns and can shut down communication.
  • Jumping to Solutions: Do not immediately suggest mittens or restraints before acknowledging the emotional impact. This can make the caregiver feel their distress is being ignored in favor of a task.
  • Minimizing Feelings: Avoid phrases like "It's common to feel this way." While intended to normalize, it can sound dismissive of the individual's unique pain.

핵심 개념

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