lunedì 11 novembre 2013

Pain Nursing Magazine - Vol. 2, Numero 3


Volume 2 - Numero 3

► Editoriale

Potenziare il Nursing per una sanità sempre più efficiente

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► Rassegna

Considerazioni infermieristiche sulla gestione del dolore episodico intenso o Breakthrough Pain

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► Rassegna

Il dolore pediatrico

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► Training and Education

Cateteri Centrali ad Inserzione Periferica (PICC): vecchio fascino, nuove tecniche, un dibattito sempre attuale

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► Formazione

Ecografia infermieristica: lo stato dell’arte

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► Caso clinico

Pseudo-infarto e dolore toracico: mimesi del carcinoma squamocellulare

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► Esperienze

Il low back pain: dalla fisiopatologia alla pratica clinica

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► Lettere

Dolore e piacere: pura antitesi?

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Dementia Caregivers' Lived Experience of Sleep


Dementia Caregivers' Lived Experience of Sleep



Clinical Nurse Specialist:
doi: 10.1097/NUR.0b013e3182a87287
Feature Article


Abstract

Purpose: Poor sleep quality leads to sleep deficiency, an unmet public health problem that is especially acute in caregivers. The purpose of this study was to investigate the dementia caregiver’s lived experience of sleep. The specific objectives were to (1) explore causes for poor sleep as identified by the caregiver, (2) gain knowledge about how the caregiver manages the sleep experience, and (3) gain an understanding of how caregivers perceive health promotion suggestions to improve sleep quality.
Methods: This was a qualitative study using a phenomenological framework. In 3 focus groups, data were collected from 15 informal/family member caregivers of a person with dementia (PWD).
Results: Three themes were identified in caregivers’ descriptions of disruptions to their sleep quality: sleep quality fluctuating with the status of the PWD, a need for vigilance to safeguard the PWD at night, and worry about current and future events, which caused rumination. Caregivers did not receive formal help from healthcare providers but did participate in activities that promote good sleep. Caregivers identified barriers to health promotion activities, including lack of time, decreased energy, and additional costs for providing care for the PWD.
Conclusion: This research provides exemplars of caregivers’ thoughts, preferences, values, and beliefs regarding their sleep experience in the context of caregiving. The caregiver’s perspective should be taken into consideration when clinical nurse specialists provide evidence-based care. Clinical implications are provided.

Management of patients with Parkinson disease


Management of patients with Parkinson disease



Nurse Practitioner:
doi: 10.1097/01.NPR.0000434090.96229.5c
Feature: DEGENERATIVE DISORDERS: CE Connection


Abstract

Patients with Parkinson disease have prolonged motor and nonmotor symptoms affecting their ability to perform activities of daily living. Providers are tasked not only to provide quality care to afflicted patients but also to offer assistance to their informal caregivers who play a critical supportive role along the illness trajectory.