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Therapeutic Methods and Therapies TCIM
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1.
Medicine (Baltimore) ; 100(21): e26099, 2021 May 28.
Article in English | MEDLINE | ID: mdl-34032747

ABSTRACT

BACKGROUND: Although home-based pulmonary rehabilitation programs have been shown in some studies to be an alternative and effective model, there is a lack of consensus in the medical literature due to different study designs and lack of standardization among procedures. Therefore, the purpose of this study was to compare the efficacy of a home-based versus outpatient pulmonary rehabilitation program for patients with chronic obstructive pulmonary disease (COPD). METHODS: Five electronic databases including Embase, PubMed, Scopus, Science Direct, and Cochrane Library will be searched in May 2021 by 2 independent reviewers. The reference lists of the included studies will be also checked for additional studies that are not identified with the database search. There is no restriction on the dates of publication or language in the search. The randomized controlled trials focusing on comparing home-based and outpatient pulmonary rehabilitation for COPD patients will be included in our meta-analysis. The following outcomes should have been measured: functional exercise capacity, disease-specific health-related quality of life, and cost-effectiveness measures. Risk ratio with a 95% confidence interval or standardized mean difference with 95% CI is assessed for dichotomous outcomes or continuous outcomes, respectively. RESULTS: It was hypothesized that these 2 methods would provide similar therapeutic benefits. REGISTRATION NUMBER: 10.17605/OSF.IO/5CV48.


Subject(s)
Ambulatory Care/organization & administration , Home Care Services, Hospital-Based/organization & administration , Pulmonary Disease, Chronic Obstructive/rehabilitation , Quality of Life , Ambulatory Care/economics , Ambulatory Care/methods , Cost-Benefit Analysis , Exercise Tolerance , Home Care Services, Hospital-Based/economics , Humans , Meta-Analysis as Topic , Pulmonary Disease, Chronic Obstructive/diagnosis , Pulmonary Disease, Chronic Obstructive/economics , Pulmonary Disease, Chronic Obstructive/psychology , Randomized Controlled Trials as Topic , Systematic Reviews as Topic , Treatment Outcome
2.
Cochrane Database Syst Rev ; 9: CD012780, 2020 09 30.
Article in English | MEDLINE | ID: mdl-32996586

ABSTRACT

BACKGROUND: Serious illness is often characterised by physical/psychological problems, family support needs, and high healthcare resource use. Hospital-based specialist palliative care (HSPC) has developed to assist in better meeting the needs of patients and their families and potentially reducing hospital care expenditure. There is a need for clarity on the effectiveness and optimal models of HSPC, given that most people still die in hospital and also to allocate scarce resources judiciously. OBJECTIVES: To assess the effectiveness and cost-effectiveness of HSPC compared to usual care for adults with advanced illness (hereafter patients) and their unpaid caregivers/families. SEARCH METHODS: We searched CENTRAL, CDSR, DARE and HTA database via the Cochrane Library; MEDLINE; Embase; CINAHL; PsycINFO; CareSearch; National Health Service Economic Evaluation Database (NHS EED) and two trial registers to August 2019, together with checking of reference lists and relevant systematic reviews, citation searching and contact with experts to identify additional studies. SELECTION CRITERIA: We included randomised controlled trials (RCTs) evaluating the impact of HSPC on outcomes for patients or their unpaid caregivers/families, or both. HSPC was defined as specialist palliative care delivered by a palliative care team that is based in a hospital providing holistic care, co-ordination by a multidisciplinary team, and collaboration between HSPC providers and generalists. HSPC was provided to patients while they were admitted as inpatients to acute care hospitals, outpatients or patients receiving care from hospital outreach teams at home. The comparator was usual care, defined as inpatient or outpatient hospital care without specialist palliative care input at the point of entry into the study, community care or hospice care provided outside of the hospital setting. DATA COLLECTION AND ANALYSIS: We used standard methodological procedures expected by Cochrane. We assessed risk of bias and extracted data. To account for use of different scales across studies, we calculated standardised mean differences (SMDs) with 95% confidence intervals (CIs) for continuous data. We used an inverse variance random-effects model. For binary data, we calculated odds ratio (ORs) with 95% CIs. We assessed the evidence using GRADE and created a 'Summary of findings' table. Our primary outcomes were patient health-related quality of life (HRQoL) and symptom burden (a collection of two or more symptoms). Key secondary outcomes were pain, depression, satisfaction with care, achieving preferred place of death, mortality/survival, unpaid caregiver burden, and cost-effectiveness. Qualitative data was analysed where available. MAIN RESULTS: We identified 42 RCTs involving 7779 participants (6678 patients and 1101 caregivers/family members). Twenty-one studies were with cancer populations, 14 were with non-cancer populations (of which six were with heart failure patients), and seven with mixed cancer and non-cancer populations (mixed diagnoses). HSPC was offered in different ways and included the following models: ward-based, inpatient consult, outpatient, hospital-at-home or hospital outreach, and service provision across multiple settings which included hospital. For our main analyses, we pooled data from studies reporting adjusted endpoint values. Forty studies had a high risk of bias in at least one domain. Compared with usual care, HSPC improved patient HRQoL with a small effect size of 0.26 SMD over usual care (95% CI 0.15 to 0.37; I2 = 3%, 10 studies, 1344 participants, low-quality evidence, higher scores indicate better patient HRQoL). HSPC also improved other person-centred outcomes. It reduced patient symptom burden with a small effect size of -0.26 SMD over usual care (95% CI -0.41 to -0.12; I2 = 0%, 6 studies, 761 participants, very low-quality evidence, lower scores indicate lower symptom burden). HSPC improved patient satisfaction with care with a small effect size of 0.36 SMD over usual care (95% CI 0.41 to 0.57; I2 = 0%, 2 studies, 337 participants, low-quality evidence, higher scores indicate better patient satisfaction with care). Using home death as a proxy measure for achieving patient's preferred place of death, patients were more likely to die at home with HSPC compared to usual care (OR 1.63, 95% CI 1.23 to 2.16; I2 = 0%, 7 studies, 861 participants, low-quality evidence). Data on pain (4 studies, 525 participants) showed no evidence of a difference between HSPC and usual care (SMD -0.16, 95% CI -0.33 to 0.01; I2 = 0%, very low-quality evidence). Eight studies (N = 1252 participants) reported on adverse events and very low-quality evidence did not demonstrate an effect of HSPC on serious harms. Two studies (170 participants) presented data on caregiver burden and both found no evidence of effect of HSPC (very low-quality evidence). We included 13 economic studies (2103 participants). Overall, the evidence on cost-effectiveness of HSPC compared to usual care was inconsistent among the four full economic studies. Other studies that used only partial economic analysis and those that presented more limited resource use and cost information also had inconsistent results (very low-quality evidence). Quality of the evidence The quality of the evidence assessed using GRADE was very low to low, downgraded due to a high risk of bias, inconsistency and imprecision. AUTHORS' CONCLUSIONS: Very low- to low-quality evidence suggests that when compared to usual care, HSPC may offer small benefits for several person-centred outcomes including patient HRQoL, symptom burden and patient satisfaction with care, while also increasing the chances of patients dying in their preferred place (measured by home death). While we found no evidence that HSPC causes serious harms, the evidence was insufficient to draw strong conclusions. Although these are only small effect sizes, they may be clinically relevant at an advanced stage of disease with limited prognosis, and are person-centred outcomes important to many patients and families. More well conducted studies are needed to study populations with non-malignant diseases and mixed diagnoses, ward-based models of HSPC, 24 hours access (out-of-hours care) as part of HSPC, pain, achieving patient preferred place of care, patient satisfaction with care, caregiver outcomes (satisfaction with care, burden, depression, anxiety, grief, quality of life), and cost-effectiveness of HSPC. In addition, research is needed to provide validated person-centred outcomes to be used across studies and populations.


Subject(s)
Caregivers/statistics & numerical data , Home Care Services, Hospital-Based/economics , Palliative Care/economics , Palliative Care/methods , Terminal Care/economics , Terminal Care/methods , Ambulatory Care/economics , Bias , Caregivers/psychology , Cost-Benefit Analysis , Family , Heart Failure/mortality , Heart Failure/therapy , Hospitalization/economics , Humans , Neoplasms/mortality , Neoplasms/therapy , Pain Management/statistics & numerical data , Patient Satisfaction , Quality of Life , Randomized Controlled Trials as Topic , Symptom Assessment/statistics & numerical data
3.
J Pediatr ; 220: 80-85, 2020 05.
Article in English | MEDLINE | ID: mdl-32067781

ABSTRACT

OBJECTIVE: To characterize home phototherapy treatment for neonatal hyperbilirubinemia and assess the risk factors associated with the need for hospital admission during or after home phototherapy. STUDY DESIGN: This was a retrospective study of newborn infants born at ≥35 weeks of gestation who underwent comprehensive home phototherapy (that included daily in-home lactation support and blood draws) over an 18-month period. We excluded infants who lacked a recorded birth date or time, started treatment at age >14 days, or had a conjugated serum bilirubin level of ≥2 mg/dL (≥34.2 µmol/L). The primary study outcome was any hospital admission during or within 24 hours after completion of home phototherapy. Logistic regression was used to identify risk factors for hospitalization. RESULTS: Of the cohort of 1385 infants, 1324 met the inclusion criteria. At the time home phototherapy was initiated, 376 infants (28%) were at or above the American Academy of Pediatrics phototherapy threshold. Twenty-five infants required hospitalization (1.9%; 95% CI, 1.3%-2.8%). Hospital admission was associated with a younger age at phototherapy initiation (OR, 0.63 for each day older in age; 95% CI, 0.44-0.91) and a higher total serum bilirubin level relative to the treatment threshold at phototherapy initiation (OR, 1.71 for each 1 mg/dL above the treatment threshold; 95% CI, 1.40-2.08). CONCLUSIONS: Comprehensive home phototherapy successfully treated hyperbilirubinemia in the vast majority of the infants in this cohort.


Subject(s)
Home Care Services, Hospital-Based , Hyperbilirubinemia, Neonatal/therapy , Phototherapy , Age Factors , Bilirubin/blood , Female , Home Care Services, Hospital-Based/economics , Humans , Infant, Newborn , Male , Patient Admission/statistics & numerical data , Phototherapy/economics , Retreatment , Retrospective Studies , Sampling Studies
4.
Transfus Clin Biol ; 26(4): 304-308, 2019 Nov.
Article in French | MEDLINE | ID: mdl-30268597

ABSTRACT

OBJECTIVES: Patients with cancers or malignant homeopathies can suffer from chronic anemia and be regularly transfused in hospitals. Most of the time, their performance status is low. Few local structures currently provide blood transfusion services and patients have to go under difficult and costing transportation to the hospital. The objective of this work is to evaluate benefits and development terms of home blood transfusion for patients with chronic anemia and having to get transfused regularly. METHODS: A field investigation-mixing observations and interviews and a literature review were conducted. RESULTS: Home blood transfusion represented a little part of home health care activity. When it was practiced, its organization was heterogeneous: it was sometimes performed by a doctor, sometimes by a nurse. Home blood transfusion was benefic for patients: it was more comfortable and it allowed them to avoid harmful transportation to the hospital. Few adverse events occurred during various experiments, all were mild. Before its revaluation in March 2018, home blood transfusion was not enough funded by National health insurance. Home blood transfusion also suffered from a lack of framework until the publication of recommendations in April 2018. CONCLUSIONS: Lack of a framework and sufficient funding prevented home blood transfusion development until changes that occurred in 2018. Therefore, this activity should develop in years to come. Allowing reducing unnecessary hospitalizations, home blood transfusion fit into French health national strategy.


Subject(s)
Blood Transfusion , Home Care Services, Hospital-Based , Anemia/etiology , Anemia/therapy , Blood Transfusion/economics , Blood Transfusion/legislation & jurisprudence , Blood Transfusion/statistics & numerical data , Chronic Disease , France , Health Care Surveys , Home Care Services, Hospital-Based/economics , Home Care Services, Hospital-Based/legislation & jurisprudence , Humans , National Health Programs , Neoplasms/complications , Patient Acceptance of Health Care , Risk Assessment
5.
J Am Med Dir Assoc ; 18(9): 780-784, 2017 Sep 01.
Article in English | MEDLINE | ID: mdl-28578883

ABSTRACT

OBJECTIVE: To compare outcomes and costs for patients with orthogeriatric conditions in a home-based integrated care program versus conventional hospital-based care. DESIGN: Quasi-experimental longitudinal study. SETTING: An acute care hospital, an intermediate care hospital, and the community of an urban area in the North of Barcelona, in Southern Europe. PARTICIPANTS: In a 2-year period, we recruited 367 older patients attended at an orthopedic/traumatology unit in an acute hospital for fractures and/or arthroplasty. INTERVENTION: Patients were referred to a hospital-at-home integrated care unit or to standard hospital-based postacute orthogeriatric unit, based on their social support and availability of the resource. MEASUREMENTS: We compared home-based care versus hospital-based care for Relative Functional Gain (gain/loss of function measured by the Barthel Index), mean direct costs, and potential savings in terms of reduction of stay in the acute care hospital. RESULTS: No differences were found in Relative Functional Gain, median (Q25-Q75) = 0.92 (0.64-1.09) in the home-based group versus 0.93 (0.59-1) in the hospital-based group, P =.333. Total health service direct cost [mean (standard deviation)] was significantly lower for patients receiving home-based care: €7120 (3381) versus €12,149 (6322), P < .001. Length of acute hospital stay was significantly shorter in patients discharged to home-based care [10.1 (7)] than in patients discharged to the postacute orthogeriatric hospital-based unit [15.3 (12) days, P < .001]. CONCLUSION: The hospital-at-home integrated care program was suitable for managing older patients with orthopedic conditions who have good social support for home care. It provided clinical care comparable to the hospital-based model, and it seems to enable earlier acute hospital discharge and lower direct costs.


Subject(s)
Arthroplasty/rehabilitation , Delivery of Health Care, Integrated/economics , Fractures, Bone/rehabilitation , Home Care Services, Hospital-Based/economics , Aged , Aged, 80 and over , Costs and Cost Analysis , Female , Hospitalization/economics , Humans , Longitudinal Studies , Male , Outcome Assessment, Health Care , Recovery of Function/physiology
6.
Semin Thorac Cardiovasc Surg ; 28(2): 574-582, 2016.
Article in English | MEDLINE | ID: mdl-28043480

ABSTRACT

The objective of the study was to evaluate the Integrated Comprehensive Care (ICC) program, a novel health system integration initiative that coordinates home care and hospital-based clinical services for patients undergoing major thoracic surgery relative to traditional home care delivery. Methods included a pilot retrospective cohort analysis that compared the intervention cohort (ICC), composed of all patients undergoing major thoracic surgery in the 2012-2013 fiscal year with a control cohort, who underwent surgery in the year before the initiation of ICC. Length of stay, hospital costs, readmission, and emergency room visit data were stratified by degree and approach of resection and compared using univariate logistic regression analysis. A total of 331 patients under ICC and 355 control patients were enrolled. Hospital stay was significantly shorter in patients under video-assisted thoracoscopic surgery (VATS) ICC (sublobar median 3 vs 4 days, P = 0.013; lobar median 4 vs 5 days, P = 0.051) but not for open resections. The frequency of emergency room visits within 60 days of surgery was lower for all stratification groups in the ICC cohort, except for VATS sublobar (25.7% control vs 13.9% ICC, P = 0.097). There were no significant differences in 60-day readmission frequency in any subcohort. The mean inpatient case cost was significantly lower for ICC VATS sublobar resections ($8505.39 vs $11,038.18, P = 0.007), with the other resection types trending lower for ICC but nonsignificant. In conclusion, a hospital-based, postdischarge, patient-centered program could potentially result in shorter hospital stay, fewer readmission and emergency room visits, costsavings, and no increase in adverse postdischarge outcomes after major thoracic surgery.


Subject(s)
Delivery of Health Care, Integrated , Home Care Services, Hospital-Based , Patient-Centered Care/methods , Thoracic Surgical Procedures/adverse effects , Aged , Chi-Square Distribution , Cost Savings , Delivery of Health Care, Integrated/economics , Emergency Service, Hospital , Female , Home Care Services, Hospital-Based/economics , Hospital Costs , Humans , Length of Stay , Logistic Models , Male , Middle Aged , Patient Discharge , Patient Readmission , Patient-Centered Care/economics , Pilot Projects , Pneumonectomy/adverse effects , Program Evaluation , Retrospective Studies , Risk Factors , Thoracic Surgery, Video-Assisted/adverse effects , Thoracic Surgical Procedures/economics , Thoracic Surgical Procedures/methods , Thoracic Surgical Procedures/mortality , Time Factors , Treatment Outcome
7.
Aten. prim. (Barc., Ed. impr.) ; 47(2): 75-82, feb. 2015. tab, graf
Article in Spanish | IBECS | ID: ibc-133649

ABSTRACT

OBJETIVO: Determinar, a partir de los análisis de los profesionales de atención domiciliaria, el grado de relevancia de las competencias no técnicas de esos profesionales dedicados a la atención de pacientes con enfermedades crónicas. DISEÑO: Investigación cuanti-cualitativa realizada en 2 fases: la 1. a entre noviembre de 2010 y marzo de 2011 y la 2. a entre diciembre de 2012 y agosto de 2013. Emplazamiento: Región Sanitaria de Barcelona ciudad. PARTICIPANTES: En la primera fase, 30 profesionales pertenecientes a 6 equipos de atención domiciliaria (3 del ámbito de la atención primaria y 3 del ámbito hospitalario). En la 2. a fase, 218 profesionales pertenecientes a 50 equipos de atención primaria (EAP) y a 7 programas deatención domiciliaria y equipos de apoyo sanitario y social (PADES). MÉTODO: Muestreo intencional en la 1. a fase y aleatorio en la 2. a. Se emplearon escalas tipo Likert y grupos focales. RESULTADOS: A partir de la identificación de 19 categorías competenciales en la 1. a fase del estudio, se establecieron, en la 2. a fase, 3 metacategorías competenciales: atención integral centrada en el paciente, organización interprofesional y entre niveles asistenciales y competencia relacional. CONCLUSIONES: Es necesario favorecer y garantizar las relaciones profesionales entre niveles asistenciales, la continuidad asistencial, la concepción biopsicosocial y la atención holística al paciente y a su entorno, contemplando emociones, expectativas, sentimientos, creencias y valores de pacientes y familiares. Es imprescindible el diseño e implementación de formación en competencias transversales en el ámbito de cada centro, a través de metodologías didácticas activas y participativas


AIM: To determine the relevance level of non-technical skills of those professionals dedicated to the healthcare of patients with chronic diseases, from an analysis of home care professionals. DESIGN: Quantitative and qualitative research conducted in 2 phases: 1. st from November 2010 to March 2011 and 2. nd from December 2012 to August 2013. SETTING: Health Region of Barcelona city. PARTICIPANTS: During the 1. st phase, 30 professionals from homecare teams (3 from Primary Care and 3 from Hospitals). In 2. nd phase, 218 professionals from 50 Primary Healthcare Centres and 7 home care programmes. Method: Purposive sampling in was used in the1st phase, and randomized sampling in the 2. nd phase. Likert scales and focus group were used. RESULTS: A total of 19 skill categories were identified in the 1. st phase. In the 2. nd phase 3 metacategories were established: comprehensive patient-centered care, interprofessional organization, and inter-health care fields and interpersonal skills. CONCLUSIONS: It is necessary to improve and secure the professionals relationships between levels of healthcare, continuity of healthcare, biopsychosocial model and holistic attention to patients and relatives, looking at emotions, expectations, feelings, beliefs and values. It is essential to design and implement continuing training in transferable skills in every healthcare centre, through active methodologies


Subject(s)
Humans , Male , Female , Home Care Services, Hospital-Based/classification , Home Care Services, Hospital-Based/ethics , Chronic Disease/classification , Societies/ethics , Societies/policies , Quality of Life/legislation & jurisprudence , Home Care Services, Hospital-Based/economics , Home Care Services, Hospital-Based/organization & administration , Home Care Services, Hospital-Based/standards , Chronic Disease/prevention & control , Societies/legislation & jurisprudence , Quality of Life/psychology
8.
Trials ; 15: 42, 2014 Jan 30.
Article in English | MEDLINE | ID: mdl-24479760

ABSTRACT

BACKGROUND: The incidence of strokes in industrialized nations is on the rise, particularly in the older population. In Canada, a minority of individuals who have had a stroke actually receive intensive rehabilitation because most stroke patients do not have access to services or because their motor recovery was judged adequate to return home. Thus, there is a considerable need to organize home-based rehabilitation services for everyone who has had a stroke. To meet this demand, telerehabilitation, particularly from a service center to the patient's home, is a promising alternative approach that can help improve access to rehabilitation services once patients are discharged home. METHODS/DESIGN: This non-inferiority study will include patients who have returned home post-stroke without requiring intensive rehabilitation. To be included in the study, participants will: 1) not be referred to an Intensive Functional Rehabilitation Unit, 2) have a Rankin score of 2 or 3, and 3) have a balance problem (Berg Balance Scale score between 46 and 54). Participants will be randomly assigned to either the teletreatment group or the home visits group. Except for the delivery mode, the intervention will be the same for both groups, that is, a personalized Tai Chi-based exercise program conducted by a trained physiotherapist (45-minute session twice a week for eight consecutive weeks). The main objective of this research is to test the non-inferiority of a Tai Chi-based exercise program provided via telerehabilitation compared to the same program provided in person at home in terms of effectiveness for retraining balance in individuals who have had a stroke but do not require intensive functional rehabilitation. The main outcome of this study is balance and mobility measured with the Community Balance and Mobility Scale. Secondary outcomes include physical and psychological capacities related to balance and mobility, participants' quality of life, satisfaction with services received, and cost-effectiveness associated with the provision of both types of services. STUDY/TRIAL REGISTRATION: ClinicalTrials.gov: NCT01848080.


Subject(s)
Exercise Therapy , Home Care Services, Hospital-Based , House Calls , Research Design , Stroke Rehabilitation , Tai Ji , Telemedicine , Canada , Clinical Protocols , Cost-Benefit Analysis , Disability Evaluation , Exercise Therapy/economics , Health Care Costs , Home Care Services, Hospital-Based/economics , House Calls/economics , Humans , Motor Activity , Patient Satisfaction , Postural Balance , Quality of Life , Recovery of Function , Stroke/diagnosis , Stroke/economics , Stroke/physiopathology , Tai Ji/economics , Telemedicine/economics , Time Factors , Treatment Outcome
9.
BMC Pulm Med ; 12: 58, 2012 Sep 19.
Article in English | MEDLINE | ID: mdl-22992240

ABSTRACT

BACKGROUND: Breathlessness is a common and distressing symptom affecting many patients with advanced disease both from malignant and non-malignant origin. A combination of pharmacological and non-pharmacological measures is necessary to treat this symptom successfully. Breathlessness services in various compositions aim to provide comprehensive care for patients and their carers by a multiprofessional team but their effectiveness and cost-effectiveness have not yet been proven. The Breathlessness Support Service (BSS) is a newly created multiprofessional and interdisciplinary outpatient service at a large university hospital in South East London. The aim of this study is to develop and evaluate the effectiveness and cost effectiveness of this multidisciplinary out-patient BSS for the palliation of breathlessness, in advanced malignant and non-malignant disease. METHODS: The BSS was modelled based on the results of qualitative and quantitative studies, and systematic literature reviews. A randomised controlled fast track trial (RCT) comprising two groups: 1) intervention (immediate access to BSS in addition to standard care); 2) control group (standard best practice and access to BSS after a waiting time of six weeks). Patients are included if suffering from breathlessness on exertion or at rest due to advanced disease such as cancer, chronic obstructive pulmonary disease (COPD), chronic heart failure (CHF), interstitial lung disease (ILD) or motor neurone disease (MND) that is refractory to maximal optimised medical management. Both quantitative and qualitative outcomes are assessed in face to-face interviews at baseline, after 6 and 12 weeks. The primary outcome is patients' improvement of mastery of breathlessness after six weeks assessed on the Chronic Respiratory Disease Questionnaire (CRQ). Secondary outcomes for patients include breathlessness severity, symptom burden, palliative care needs, service use, and respiratory measures (spirometry). For analyses, the primary outcome, mastery of breathlessness after six weeks, will be analysed using ANCOVA. Selection of covariates will depend on baseline differences between the groups. Analyses of secondary outcomes will include patients' symptom burden other than breathlessness, physiological measures (lung function, six minute walk distance), and caregiver burden. DISCUSSION: Breathlessness services aim to meet the needs of patients suffering from this complex and burdensome symptom and their carers. The newly created BSS is different to other current services as it is run in close collaboration of palliative medicine and respiratory medicine to optimise medical care of patients. It also involves professionals from various medical, nursing, physiotherapy, occupational therapy and social work background. TRIAL REGISTRATION: ClinicalTrials.gov (NCT01165034).


Subject(s)
Ambulatory Care/methods , Dyspnea/therapy , Home Care Services, Hospital-Based/economics , Patient Care Team/economics , Program Development/economics , Aged , Cost-Benefit Analysis , Dyspnea/economics , Dyspnea/etiology , Female , Heart Failure/complications , Humans , London , Lung Neoplasms/complications , Male , Middle Aged , Pulmonary Disease, Chronic Obstructive/complications , Treatment Outcome
10.
Med Klin Intensivmed Notfmed ; 107(3): 185-91, 2012 Apr.
Article in German | MEDLINE | ID: mdl-22415450

ABSTRACT

Non-invasive mechanical ventilation is the preferred method for the treatment of acute respiratory failure in patients with chronic obstructive pulmonary disease (COPD). Primary contraindications and stopping criteria must be regarded to avoid delaying endotracheal intubation. The primary interface is usually a nasal-oral mask. Cautious sedation can facilitate non-invasive ventilation in some patients. Under certain circumstances non-invasive ventilation may enable successful extubation in COPD patients with prolonged weaning. COPD patients can also benefit from preventive non-invasive ventilation in order to avoid re-intubation after a planned extubation. Domiciliary nocturnal non-invasive ventilation is an option for some patients with COPD in chronic hypercapnic respiratory failure. This treatment should be established in a specialised unit.


Subject(s)
Continuous Positive Airway Pressure/methods , Intensive Care Units , Pulmonary Disease, Chronic Obstructive/therapy , Conscious Sedation/economics , Continuous Positive Airway Pressure/economics , Contraindications , Cost Savings , Germany , Guideline Adherence , Home Care Services, Hospital-Based/economics , Humans , Hypercapnia/economics , Hypercapnia/therapy , Intensive Care Units/economics , Intubation, Intratracheal/economics , Length of Stay/economics , National Health Programs/economics , Pulmonary Disease, Chronic Obstructive/economics , Respiratory Insufficiency/economics , Respiratory Insufficiency/therapy , Ventilator Weaning
11.
Women Birth ; 25(4): 152-8, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22104264

ABSTRACT

BACKGROUND: Publicly-funded homebirth programs in Australia have been developed in the past decade mostly in isolation from each other and with limited published evaluations. There is also distinct lack of publicly available information about the development and characteristics of these programs. We instigated the National Publicly-funded Homebirth Consortium and conducted a preliminary survey of publicly-funded homebirth providers. AIM: To outline the development of publicly-funded homebirth models in Australia. METHODS: Providers of publicly-funded homebirth programs in Australia were surveyed using an on-line survey in December 2010. Questions were about their development, use of policy and general operational issues. A descriptive analysis of the quantitative data and content analysis of the qualitative data was undertaken. FINDINGS: In total, 12 programs were identified and 10 contributed data to this paper. The service providers reported extensive multidisciplinary consultation and careful planning during development. There was a lack of consistency in data collection throughout the publicly-funded homebirth programs due to different databases, definitions and the use of different guidelines. DISCUSSION: Publicly-funded homebirth services followed different routes during their development, but essentially had safety and collaboration with stakeholders, including women and obstetricians, as central to their process. CONCLUSION: The National Publicly-funded Homebirth Consortium has facilitated a sharing of resources, processes of development and a linkage of homebirth services around the country. This analysis has provided information to assist future planning and developments in models of midwifery care. It is important that births of women booked to these programs are clearly identified when their data is incorporated into existing perinatal datasets.


Subject(s)
Financial Support , Home Care Services, Hospital-Based/economics , Home Childbirth/economics , Maternal Health Services/economics , Midwifery/economics , Australia , Delivery, Obstetric , Female , Home Care Services, Hospital-Based/statistics & numerical data , Home Childbirth/statistics & numerical data , Hospitals, Public , Humans , Models, Nursing , Practice Guidelines as Topic , Pregnancy , Program Development , Program Evaluation , Qualitative Research
12.
Aten. prim. (Barc., Ed. impr.) ; 42(5): 278-283, mayo 2010. tab, graf
Article in Spanish | IBECS | ID: ibc-85232

ABSTRACT

ObjetivoDescribir la atención domiciliaria que ofrecen los equipos móviles de rehabilitación-fisioterapia (EMRF) como respuesta a las necesidades de la población dependiente, las características que tiene su aplicación y las consecuencias que produce sobre el paciente y su independencia funcional.DiseñoEstudio descriptivo transversal desde 2004 hasta junio de 2007.EmplazamientoMedio comunitario. Los EMRF de atención primaria en Almería.ParticipantesEn total 1.093 pacientes incluidos en el programa.Mediciones principalesSe recogió sistemáticamente el estado de salud de los pacientes (proceso discapacitante principal, motivos de inclusión en el tratamiento, valoración funcional inicial y final e índice de Barthel), los datos sobre la atención fisioterapéutica y el n.o de sesiones.ResultadosUn 64,2% de la muestra fueron mujeres; la edad media fue de 78 años. El tiempo medio de espera para su valoración fue de 4 días y hubo una gran diversidad de procesos discapacitantes principales que han quedado descritos. Existió un elevado porcentaje de síntomas de grave deterioro motor, dolor y debilidad muscular. El 88,6% de los pacientes realizó tratamiento fisioterapéutico; el 11,1% de los pacientes fisioterapia y tratamiento ocupacional y el 0,3% de los pacientes tratamiento ortésico. El número medio de sesiones fue de 12,85. Se describe la variación en el índice de Barthel final tras la intervención realizada (cinesiterapia [61,9%]; combinada con electroterapia [10,2%]; cinesiterapia y educación al cuidador [14,5%], etc.).ConclusionesSe aporta información valiosa respecto a las características de la población geriátrica y dependiente así como la ayuda fisioterapéutica que viene recibiendo y cómo se lleva a cabo el proceso(AU)


ObjectiveTo describe the home care provided by mobile rehabilitation-physiotherapy teams as a response to the needs of the dependent population, the characteristics of their application, and the results they have on patients and their functional independence.DesignA descriptive, cross-sectional study from 2004 to June 2007.SettingCommunity setting. Mobile rehabilitation-physiotherapy teams from Primary Care in Almeria.ParticipantsA total of 1093 patients were included in the programme.Main measurementsData were collected on, the state of the patients’ health (primary disabling process, reasons for inclusion in the treatment, initial and final functional assessment and Barthel Index); details of physiotherapy treatment, and number of sessions.ResultsOf the total sample, the mean age was 78 years and 64.2% were female. The mean waiting time for their assessment was 4 days and there was a wide variety of primary disabling processes described. There was a high percentage of symptoms of severe motor deterioration, pain and muscle weakness. Physiotherapy treatment was given in 88.6%, physiotherapy and occupational therapy in 11.1%, and orthopaedic treatment in 0.3%, of the patients. The mean number of sessions was 12.85. The variation in the Barthel Index after the final therapy was given was, 61.9% for kinesiotherapy, 10.2% combined with electrotherapy, and 14.5% for kinesiotherapy and carer education.ConclusionsValuable information is provided as regards the characteristics of the geriatric and dependent population, as well as the physiotherapy help they are receiving, and also how the procedure is carried out(AU)


Subject(s)
Humans , Male , Female , Aged , Physical Therapy Department, Hospital/classification , Physical Therapy Department, Hospital/ethics , Physical Therapy Department, Hospital , Physical Therapy Department, Hospital/organization & administration , Physical Therapy Department, Hospital/statistics & numerical data , Physical Therapy Department, Hospital/trends , Physical Therapy Specialty/education , Physical Therapy Specialty/statistics & numerical data , Home Care Services, Hospital-Based/economics , Home Care Services, Hospital-Based/ethics , Home Care Services, Hospital-Based , Home Care Services, Hospital-Based/organization & administration , Home Care Services, Hospital-Based/supply & distribution , Home Care Services, Hospital-Based/statistics & numerical data , Home Care Services, Hospital-Based/trends , Home Care Services, Hospital-Based
13.
Support Care Cancer ; 15(1): 101-4, 2007 Jan.
Article in English | MEDLINE | ID: mdl-16941134

ABSTRACT

PURPOSE: Children suffering from cancer often have to undergo physiotherapy that either extends the duration of in-patient hospitalisation or requires more frequent visits to the outpatient clinic. To improve care and to decrease the length of hospitalisation of children being treated at the Dept. of Haematoloy/Oncology of the Gaslini Children's Hospital, a programme of Home Care was set up in April 2000. MATERIALS AND METHODS: In June 2003, rehabilitation was added to the procedures that were feasible at home and included i.v. therapy administration, blood examinations, transfusion and/or psychological support, as well as palliative care for terminally ill children. The physiotherapy sessions were done in the ward, in the Rehabilitation Unit Gym, or at home, depending on the clinical conditions and the needs of the child and the family. RESULTS: Between June 2003 and May 2005, 46 children, whose median age was 7 years (range 6 months-21 years) suffering from CNS tumours (13), leukaemia (13), neuroblastoma (7), bone tumours (6), sarcoma (4) and lymphoma (3), underwent 1,398 physiotherapy sessions for neuro-motor re-education (534), motor rehabilitation (485), strain re-education and training (250), respiratory care (79), or to improve comfort during the terminal phase of the disease (50). To maintain continuity of care, the treatments were performed at home (931), in the hospital ward (282), or in the gymnasium of our Physiotherapy Service (185). CONCLUSION: The physiotherapist was able to start or to continue assistance at home or in the hospital, and to keep up the programme based on the child's needs. Integrated home/hospital physiotherapy for children suffering from cancer is feasible and is useful for maintaining continuity of treatment without lengthening hospitalisation.


Subject(s)
Home Care Services, Hospital-Based/organization & administration , Hospitalization , Neoplasms/rehabilitation , Physical Therapy Modalities/organization & administration , Adolescent , Adult , Child , Child, Preschool , Delivery of Health Care, Integrated , Feasibility Studies , Female , Home Care Services, Hospital-Based/economics , Hospitalization/economics , Humans , Infant , Male , Neoplasms/economics , Physical Therapy Modalities/economics
14.
Br J Dermatol ; 147(5): 957-65, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12410707

ABSTRACT

BACKGROUND: While most patients requiring phototherapy can attend for hospital-based out-patient ultraviolet (UV) B therapy, a significant number cannot attend because of geographical, work, economic and other reasons. OBJECTIVES: To determine whether there was a need for home phototherapy in the Tayside area and, if so, to establish protocols and then to assess if such a service would be workable. METHODS: Patients referred from dermatology out-patient clinics in Tayside for narrow-band UVB (TL-01) phototherapy completed a pilot questionnaire that was followed by a two-phase project. In phase 1, patients with psoriasis were trained to use the home phototherapy equipment (HoPE) within the hospital department under nursing supervision while a teaching package and protocols were developed. In phase 2, home phototherapy was made available for patient use in the community, supported by a specialist home phototherapy nurse. Waldmann UV100 home therapy units were used, with accurate dosimetry. Detailed treatment records were kept and questionnaires were used to assess acceptability and costs of therapy. RESULTS: Fifty-two pilot questionnaires were completed. Forty-two per cent of respondents found hospital phototherapy inconvenient and 75% felt phototherapy at home would be helpful. In phase 1, seven of 10 patients trained to use the HoPE completed therapy with the HoPE unit alone, reaching minimal residual activity (MRA) or clearance in a median of 18 exposures (median dose 10.38 J cm-2). In phase 2, 32 courses of home phototherapy were given to 30 patients. Of 23 with psoriasis, 18 reached clearance or MRA in a median of 22.5 exposures (median dose 9.84 J cm-2). Although self-reported erythema rates appeared higher than expected, all post-treatment questionnaire respondents would choose home phototherapy over hospital therapy if required in the future. CONCLUSIONS: UVB (TL-01) home phototherapy is a useful practical development that has fulfilled a need in our catchment area. Where appropriate training and support teams are available it appears to be similar in effectiveness to hospital therapy, to be safe and to be cost-effective for patients.


Subject(s)
Home Care Services, Hospital-Based/organization & administration , Psoriasis/radiotherapy , Ultraviolet Therapy/methods , Adult , Aged , Cost of Illness , Erythema/etiology , Health Care Costs , Home Care Services, Hospital-Based/economics , Humans , Middle Aged , Outpatient Clinics, Hospital , Patient Satisfaction , Pilot Projects , Psoriasis/economics , Radiation Injuries/etiology , Scotland , Surveys and Questionnaires , Ultraviolet Therapy/adverse effects , Ultraviolet Therapy/economics
16.
J Health Serv Res Policy ; 6(3): 133-8, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11467269

ABSTRACT

OBJECTIVES: To identify factors that influence the cost-effectiveness of hospital-in-the-home (HITH) and to discuss the impact of funding arrangements in creating incentives or disincentives for the establishment of HITH services. METHODS: A review of HITH services in Australia was undertaken. Based on the review, factors affecting the relative costs of HITH and conventional care were identified, in particular, the effect of funding and organisational arrangements on the incentives for managers and providers to choose between HITH and conventional care. RESULTS: The review of HITH services identified a wide range of models of HITH in Australia. Factors identified as important to the success of HITH included demographic and location issues, referral mechanisms, the choice of staffing and the management of the programme. However, it was clear that the structure of the programme often related to funding arrangements. Issues such as 'incentive funding', establishment costs and opportunity for cost-shifting were identified as being relevant to incentives for the efficient provision of HITH. CONCLUSIONS: Evaluations are essential to inform decisions about whether HITH is likely to be a viable and cost-effective alternative to inpatient care. However, the relative costs of HITH and conventional care will depend on local factors. From the point of view of the decision-maker, these will be affected by funding and organisational arrangements. Funders must be aware that complex financial incentives may mask the true costs of HITH services relative to hospital services. They need to ensure that the incentives created by funding arrangements are transparent.


Subject(s)
Home Care Services, Hospital-Based/economics , Australia , Cost-Benefit Analysis , Health Services Research , Home Care Services, Hospital-Based/organization & administration , National Health Programs , Program Evaluation
17.
Am Surg ; 65(4): 303-6, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10190350

ABSTRACT

A home health care (HHC) referral should link the patient in a cost-effective fashion to the physician, home care, and instructions regarding ulcer management. Twenty-one patients (mean age, 74.6 years) had stage III pressure ulcers (<100 cm2) and an involved family member at home. Risk and contributing factors included cardiac disease (n = 9), hypertension (n = 14), end-stage renal disease (n = 7), smoking (n = 11), diabetes (n = 8), chronic brain syndrome (n = 14), cerebrovascular accident (n = 5), and above-the-knee amputation (n = 2). Treatment regimens included standard wound care, pressure relief and, where appropriate, culture-specific antibiotics, as well as a rehabilitation program. Home care progressively decreased the frequency of the nurse HHC and physician office visits. Resolution of the pressure ulcer varied from 6 to 32 weeks. Only two patients had progression of their wound and required hospital readmission. The billable fees included: 1) an office visit, $30.00 (medicare reimbursement, $14.00); 2) the HHC nurse visit, $159.00 (medicare reimbursement, $105.00); 3) supplies, $75.00 to $150.00/week (variable reimbursement); 4) hospitalization, $400.00 to $900.00/day; and 5) a chronic-care bed, $400.00 to $750.00/day. HHC, given a responsible support team and an involved family member, was more socially and financially acceptable than an inpatient facility. Intermittent physician visits with HHC proved safe and reliable, with 90 per cent successfully healing their wounds.


Subject(s)
Home Care Services, Hospital-Based , Hospitalization , Pressure Ulcer/therapy , Aged , Costs and Cost Analysis , Female , Home Care Services, Hospital-Based/economics , Home Nursing , Hospitalization/economics , Humans , Male , Middle Aged , Pressure Ulcer/complications , Pressure Ulcer/economics , Risk Factors
18.
Caring ; 16(10): 28-30, 32, 34-6, 1997 Oct.
Article in English | MEDLINE | ID: mdl-10173930

ABSTRACT

Recent reforms in the Dutch health care system have dramatically changed the role of and relationship between hospitals and home care organizations. These changes have fostered a more active role for hospitals in the delivery of home care services.


Subject(s)
Delivery of Health Care, Integrated/organization & administration , Home Care Services, Hospital-Based/organization & administration , Cancer Care Facilities/organization & administration , Community Health Planning/organization & administration , Cooperative Behavior , Delivery of Health Care, Integrated/economics , Health Care Reform , Home Care Services, Hospital-Based/economics , National Health Programs/organization & administration , Netherlands , Rate Setting and Review
19.
Inquiry ; 33(1): 30-41, 1996.
Article in English | MEDLINE | ID: mdl-8774372

ABSTRACT

This study measures the impact of integrated community nursing services on hospital use and costs for elderly people in a health maintenance organization (HMO). We tracked 4,943 HMO patients over three consecutive five-month periods (one preintervention and two postintervention). We compared 326 patients who entered a program of integrated services during period 2 with 301 patients who entered during period 3 and 4,316 nonprogram patients in respect to their utilization and costs during periods 2 and 3. Regression results reveal that patients receiving integrated services had significantly higher utilization and costs during the period of enrollment and significantly lower utilization and costs during the period following enrollment, compared to nonprogram patients. These results were replicated when considering only patients with observed episodes of care in these periods, when controlling for hospital use and costs in the prior period, and when controlling for the risk of selection into the program. The findings suggest that integrating services at the community level may achieve substantial cost savings.


Subject(s)
Case Management/organization & administration , Community Health Nursing/organization & administration , Delivery of Health Care, Integrated/organization & administration , Health Maintenance Organizations/organization & administration , Home Care Services, Hospital-Based/organization & administration , Hospitalization/statistics & numerical data , Medicare/organization & administration , Aged , Capitation Fee , Case Management/economics , Community Health Nursing/economics , Cost Savings , Female , Health Maintenance Organizations/economics , Health Services Research , Home Care Services, Hospital-Based/economics , Hospitalization/economics , Humans , Male , Nursing Evaluation Research , Regression Analysis , Southwestern United States , United States
20.
Med J Aust ; 162(5): 249-53, 1995 Mar 06.
Article in English | MEDLINE | ID: mdl-7891605

ABSTRACT

OBJECTIVE: To assess the practicality, safety, cost effectiveness and outcome of receiving intravenous antibiotics at home. METHODS: Patients with serious bacterial infections requiring parenteral antibiotic therapy were enrolled in a pilot program to receive treatment at home. Antibiotics were premixed in the hospital pharmacy and administered by the Royal District Nursing Service, and medical back-up was provided. RESULTS: Twenty patients (mean age, 58 years; range, 19-84 years) received 21 courses of intravenous antibiotics at home (mean duration +/- SD, 26 +/- 9 days; range, 11-44 days). Conditions treated included osteomyelitis (10 patients), endocarditis (5), vascular graft and pacemaker sepsis (4), and chronic cellulitis (1). Treatment at home was well tolerated with no significant complications, and cure was achieved in 18 of the 20 patients. It was both efficient and cost effective, with a mean benefit in treatment costs between home and the equivalent inpatient therapy of at least $112 per day for the 538 days that home therapy was provided. Moreover, the reduced bed use could allow an additional hospital throughput of between 86 and 107 patients annually. CONCLUSIONS: Home intravenous antibiotic therapy is safe, effective and well tolerated. It allows more efficient inpatient care and reduces total treatment costs in an important subpopulation of patients.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Bacterial Infections/drug therapy , Home Infusion Therapy , Adult , Aged , Aged, 80 and over , Bacterial Infections/microbiology , Cost-Benefit Analysis , Home Care Services, Hospital-Based/economics , Home Infusion Therapy/economics , Humans , Infusions, Intravenous , Length of Stay , Middle Aged , Outcome Assessment, Health Care , Pilot Projects , Victoria
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