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1.
Clin Kidney J ; 16(8): 1307-1315, 2023 Aug.
Article in English | MEDLINE | ID: mdl-37529648

ABSTRACT

Background: Chronic kidney disease-associated pruritus (CKD-aP) is a common, distressing complaint in patients with advanced renal disease that is frequently overlooked. Treatment is often unsatisfactory. Balneum Plus (Almirall, Barcelona, Spain) is a cream containing 3% lauromacrogols and 5% urea, commonly used to treat atopic dermatitis. It has not been studied in CKD-aP to date. Methods: Adult haemodialysis patients were randomised 1:1 to apply Balneum Plus or E45 (Reckitt Beckiser, Slough, UK) to compare the active ingredients of lauromacrogol and urea with a control cream. Itch was defined as three episodes of itching during the last 2 weeks, appearing a few times a day, lasting a few minutes and troubling the patient [1]. Patients with other causes of itch, e.g. eczema and liver disease, were excluded. The primary outcome was a reduction in itch as measured by the visual analogue scale (VAS) score at 4 weeks and analysed using an analysis of covariance approach. Results: A total of 314 patients were screened and 58 patients were randomised, 29 in each group. Three patients dropped out in each group. The median baseline VAS scores were 6.5 [interquartile range (IQR) 4.4-8.0] in the Balneum Plus group and 6.3 (IQR 5.1-7.3) in the E45 group. After 4 weeks, VAS scores decreased to 2.6 (IQR 0.9-4.5) and 2.0 (IQR 0.5-4.8) in the Balneum Plus and E45 groups respectively (P = 0.64 for the difference). Using a validated questionnaire to assess secondary outcomes, we found that the Balneum Plus group had longer itching episodes, more difficulty staying asleep and itching was more annoying than in the E45 group. There was no significant difference in adverse events between the two groups. One patient reported inflamed spots on the abdominal skin in the Balneum Plus group. Conclusion: This is the first randomised controlled study of two different emollients for the treatment of CKD-aP and is a negative study. We found no significant difference in itch scores between Balneum Plus and E45.

2.
N C Med J ; 73(1): 48-50, 2012.
Article in English | MEDLINE | ID: mdl-22619855

ABSTRACT

Improving transitional care from hospital to home requires comprehensive and highly coordinated intervention during the immediate days following discharge. The Hospital to Home Program addresses both medical and social needs, prevents unnecessary readmissions, promotes improvements in patient perceptions of physical and mental health, and results in excellent patient satisfaction.


Subject(s)
Continuity of Patient Care/organization & administration , Evidence-Based Practice , Home Care Services, Hospital-Based/organization & administration , Patient Discharge/standards , Patient Readmission/standards , Activities of Daily Living , Aged , Chronic Disease , Comorbidity , Continuity of Patient Care/standards , Home Care Services, Hospital-Based/standards , Humans , North Carolina , Quality Indicators, Health Care/standards , Risk Assessment/methods , Social Support
3.
Prof Case Manag ; 17(3): 117-23; quiz 124-5, 2012.
Article in English | MEDLINE | ID: mdl-22488341

ABSTRACT

PURPOSE OF STUDY: This study describes a social-worker navigator transitional care model for at-risk seniors being discharged from hospital to home. The model is designed to prevent rehospitalizations so as to improve quality of life and patient outcomes. This model is different from others with its focus on the psychosocial aspects of care transitions, medical needs, and individualized needs with the provision of nonreimbursable services. PRIMARY PRACTICE SETTING: Care begins in the acute care hospital or inpatient rehabilitation facility and continues in the postdischarge home environment. Participants are connected to community services to support their independent living at home. METHODOLOGY AND SAMPLE: Case managers, physicians, or others refer potential participants to the navigator. Criteria for inclusion include the following: age 65 years or older, Medicare and/or Medicaid recipient, living in the same county as the hospital, and having at least 2 of a list of 11 criteria that predict readmission. After the participant agrees to enroll, the navigator recommends in-home services at discharge. Within the first 72 hr, the navigator makes a home visit to evaluate the home environment, assess medical management, and make referrals for other services. Follow-up phone calls and other home visits are made by the navigator during the participant's enrollment, which is from 30 days to 4 months. RESULTS: Hospital readmissions were decreased by 61% for this high-risk population. Cost savings by preventing readmissions correlated to a cost savings of $628,202 per year. The 36-Item Short-Form Health Survey showed statistically significant improvements in quality-of-life scores for both physical and mental health summary scales and for all 8 subscales (p < .004). Almost all (99%) of respondents were satisfied with the overall Hospital to Home program. IMPLICATIONS FOR CASE MANAGEMENT PRACTICE: The results of this study demonstrate the importance of extending social support and health education into the home after discharge from the hospital. Access to immediate in-home care services such as transportation, housekeeping, laundry, and light meal preparation allows patients not to experience gaps in care that could result in a readmission. The assigned navigator reinforces medical management and connects participants to appropriate community resources in order to remain safe at home.


Subject(s)
Case Management , Continuity of Patient Care , Frail Elderly/psychology , Health Transition , Patient Discharge , Program Evaluation , Aged , Aged, 80 and over , Chronic Disease , Female , Health Care Surveys , Health Services Needs and Demand , Humans , Male , Program Development , Quality of Health Care , Quality of Life , Risk , Social Work , Statistics as Topic
4.
Dysphagia ; 21(4): 243-53, 2006 Oct.
Article in English | MEDLINE | ID: mdl-17216386

ABSTRACT

This study compares the outcomes using VitalStim therapy to outcomes using traditional swallowing therapy for deglutition disorders. Twenty-two patients had an initial and a followup videofluoroscopic swallowing study or fiberoptic endoscopic evaluation of swallowing and were divided into an experimental group that received VitalStim treatments and a control group that received traditional swallowing therapy. Outcomes were analyzed for changes in oral and pharyngeal phase dysphagia severity, dietary consistency restrictions, and progression from nonoral to oral intake. Results of chi(2) analysis showed no statistically significant difference in outcomes between the experimental and control groups.


Subject(s)
Deglutition Disorders/diagnosis , Deglutition Disorders/therapy , Otolaryngology/methods , Adolescent , Aged , Aged, 80 and over , Female , Fluoroscopy/instrumentation , Humans , Male , Middle Aged , Mouth/physiology , Pharynx/physiology , Treatment Outcome , Videotape Recording
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