Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 51
Filter
1.
Dysphagia ; 35(1): 32-41, 2020 02.
Article in English | MEDLINE | ID: mdl-30859305

ABSTRACT

The purpose of the study is to describe experiences of swallowing with two forms of noninvasive positive-pressure ventilation (NPPV): mouthpiece NPPV (M-NPPV) and nasal bilevel positive airway pressure (BPAP) in people with muscular dystrophy. Ten men (ages 22-42 years; M = 29.3; SD = 7.1) with muscular dystrophy (9 with Duchenne's; 1 with Becker's) completed the Eating Assessment Tool (EAT-10; Ann Otol Rhinol Laryngol 117(12):919-924 [33]) and took part in semi-structured interviews. The interviews were audio recorded, transcribed, and verified. Phenomenological qualitative research methods were used to code (Dedoose.com) and develop themes. All participants affirmed dysphagia symptoms via responses on the EAT-10 (M = 11.3; SD = 6.38; Range = 3-22) and reported eating and drinking with M-NPPV and, to a lesser extent, nasal BPAP. Analysis of interview data revealed three primary themes: (1) M-NPPV improves the eating/drinking experience: Most indicated that using M-NPPV reduced swallowing-related dyspnea. (2) NPPV affects breathing-swallowing coordination: Participants described challenges and compensations in coordinating swallowing with ventilator-delivered inspirations, and that the time needed to chew solid foods between ventilator breaths may lead to dyspnea and fatigue. (3) M-NPPV aids cough effectiveness: Participants described improved cough strength following large M-NPPV delivered inspirations (with or without breath stacking). Although breathing-swallowing coordination is challenging with NPPV, participants reported that eating and drinking is more comfortable than when not using it. Overall, eating and drinking with NPPV delivered via a mouthpiece is preferred and is likely safer for swallowing than with nasal BPAP. M-NPPV (but not nasal BPAP) is reported to improve cough effectiveness, an important pulmonary defense in this population.


Subject(s)
Deglutition Disorders/therapy , Muscular Dystrophies/psychology , Noninvasive Ventilation/psychology , Patient Acceptance of Health Care/psychology , Positive-Pressure Respiration/psychology , Adult , Cannula , Deglutition , Deglutition Disorders/etiology , Deglutition Disorders/psychology , Humans , Male , Mouth , Muscular Dystrophies/complications , Muscular Dystrophies/physiopathology , Noninvasive Ventilation/instrumentation , Noninvasive Ventilation/methods , Nose , Positive-Pressure Respiration/instrumentation , Positive-Pressure Respiration/methods , Qualitative Research , Young Adult
2.
Medicine (Baltimore) ; 97(43): e12877, 2018 Oct.
Article in English | MEDLINE | ID: mdl-30412081

ABSTRACT

RATIONAL: Chronic obstructive pulmonary disease (COPD) impairs lung function and induces systemic effects, resulting in impaired quality of life. Skeletal muscle dysfunction-characteristic of advanced COPD patients-limits a patient's ability to perform activities of daily living (ADL). In addition, dysphagia is commonly observed in COPD patients. PATIENT CONCERN: This case report documents a 42-year-old man with very severe COPD. He experienced aggravation of the symptoms during standard medical treatment and his ability to perform the ADL was significantly impaired. Furthermore, his dysphagia worsened despite oromotor training. DIAGNOSIS: He was diagnosed as very severe COPD have a problem with swallowing and respiratory function. INTERVENTION: Upon NIPPV treatment, the patient's ability to perform the ADL, as well as his dysphagia, showed improvement. OUTCOMES: Thus, we report the remarkable improvement of physical function, as well as dysphagia, in a very severe COPD patient after NIPPV treatment. LESSONS: NIPPV may be useful as a treatment option for such patients.


Subject(s)
Positive-Pressure Respiration/methods , Pulmonary Disease, Chronic Obstructive/diagnosis , Pulmonary Disease, Chronic Obstructive/therapy , Activities of Daily Living/psychology , Adult , Bone Marrow Transplantation/adverse effects , Deglutition Disorders/etiology , Deglutition Disorders/physiopathology , Disease Progression , Humans , Male , Noninvasive Ventilation/methods , Noninvasive Ventilation/psychology , Oxygen/therapeutic use , Positive-Pressure Respiration/psychology , Pulmonary Disease, Chronic Obstructive/physiopathology , Quality of Life/psychology , Respiratory Function Tests/methods , Treatment Outcome
3.
Respir Care ; 61(8): 1023-32, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27118876

ABSTRACT

BACKGROUND: Research on subthreshold compliance with positive airway pressure (PAP) therapy in sleep apnea patients may inform clinical sleep medicine practice. We retrospectively assessed compliant and subthreshold compliant sleep apnea subjects to test whether regular but fewer hours of PAP use would demonstrate clinically meaningful improvements and correlate with outcomes. METHODS: A chart review was conducted of 113 consecutive sleep apnea subjects, naive to treatment, who completed a titration study and filled a PAP therapy prescription. Objective data categorized subjects into 3 groups: compliant, subthreshold compliant, and minimal use. Outcome measures assessed changes in insomnia, sleepiness, and nocturia on average 7 months from PAP initiation. Correlation coefficients analyzed dose-response relationships between hours of use and changes in outcomes. RESULTS: Among 113 PAP attempters, 104 (92%) were current users. Among 93 users with objective data, regular (consistent) PAP users included 59 compliant and 21 subthreshold compliant, and 13 subjects were minimal users. Compliant users averaging 6.6 ± 1.3 h/night and 42.0 ± 12.1 h/week showed the largest outcome improvements (all P < .05) with moderate to large effects for insomnia (d = 0.94), sleepiness (d = 0.58), and nocturia (d = 0.56). Subthreshold users averaging 4.1 ± 0.7 h/night but only 18.0 ± 5.6 h/week showed a large effect for insomnia (d = 0.76, P = .03) and nonsignificant, small effects for sleepiness (d = 0.38) and nocturia (d = 0.22). Correlation coefficients showed a trend for decrease in insomnia (P = .08; r = .20) and a significant decrease in nocturia (P = .034; r = 0.25), each in association with hours of PAP use. CONCLUSIONS: In a clinical sample, 86% of sleep apnea subjects regularly used PAP, but adherence was 63%. Regular users showed clinical treatment effects and potential dose-response relationships, suggesting that the term use offers advantages over the term adherence. Currently, subthreshold compliance may not merit insurance coverage in many countries, an issue affecting many sleep apnea patients.


Subject(s)
Patient Compliance/statistics & numerical data , Positive-Pressure Respiration/statistics & numerical data , Sleep Apnea, Obstructive/therapy , Adult , Humans , Positive-Pressure Respiration/methods , Positive-Pressure Respiration/psychology , Retrospective Studies , Sleep Apnea, Obstructive/psychology , Time Factors , Treatment Outcome
4.
Sleep Breath ; 19(1): 327-34, 2015 Mar.
Article in English | MEDLINE | ID: mdl-24989482

ABSTRACT

BACKGROUND: Obstructive sleep apnea syndrome (OSAS) is a serious disorder with significant health consequences. Treatment adherence to auto-titrating positive airway pressure (APAP) is often below expectations. We investigated the effectiveness of a brief educational intervention using motivational strategies in treatment adherence among patients with OSAS. METHODS: The study followed a randomized, controlled design and included 61 patients diagnosed with OSAS, meeting the criteria for APAP therapy. Patients recruited from a Sleep Disorders Unit were randomly allocated to an intervention group (IG) and two control groups (CG1 and CG2). In the IG motivational strategies were applied according to patient's motivation, assessed by the degree of confidence and conviction. In the CG1, participants received exclusively standardized information, and in the CG2, routine procedures were followed. Assessment included the Apnea Hypopnea Index (AHI), the Epworth Sleepiness Scale (ESS), and sociodemographic and clinical information. Adherence to treatment was measured after 1 (T1) and 2 months (T2) through the APAP software. RESULTS: The IG presented higher adherence to APAP-percentage of days of use >4 h (89.8 % p = 0.013), mean effective use per effective day (6.2 p = 0.000), and lower AHI (2.7 p = 0.019) at T2 when compared with the other two groups. Confidence was higher in the IG group at T2 than at T1 (p = 0.000). The ESS presented a significant reduction (p = 0.000) in the IG and in the CG1 (p = 0.008), but was higher in the CG2 (p = 0.015). CONCLUSIONS: Brief interventions using motivational strategies can improve a patient's adherence to APAP.


Subject(s)
Motivational Interviewing/methods , Patient Compliance/psychology , Patient Education as Topic/methods , Positive-Pressure Respiration/psychology , Sleep Apnea, Obstructive/psychology , Sleep Apnea, Obstructive/therapy , Adult , Aged , Female , Humans , Male , Middle Aged , Polysomnography , Positive-Pressure Respiration/instrumentation
5.
Psychol Health Med ; 19(1): 59-69, 2014.
Article in English | MEDLINE | ID: mdl-23484461

ABSTRACT

Adherence is still an important issue considering new advances in Obstructive Sleep Apnea (OSA) treatment, as automatic positive airway pressure (APAP). The aim of the present study was to identify and explore relationships between identified predictors of adherence, over time. After overnight sleep study and OSA diagnosis and during a six-month APAP treatment period, a total of 153 patients underwent a three time psychological protocol evaluation. Generalized estimating equations were applied to analyzed repeated measurements in the same individuals. Results show that 40% of patients were poorly adherent and 60% were adherent after six months of treatment. The results confirmed a predictive value of age, self-efficacy, decisional balance index and health-related quality of life (HRQoL) in APAP adherence. Furthermore, the results revealed an interaction between time and illness cognitive representations, and self-efficacy and family coping, in explaining adherence patterns over time. Therefore, understanding the causality of theoretically derived constructs is crucial to predict the continuity of APAP adherence.


Subject(s)
Adaptation, Psychological , Family Health , Models, Statistical , Patient Compliance/statistics & numerical data , Positive-Pressure Respiration/psychology , Sleep Apnea, Obstructive/psychology , Age Factors , Female , Health Knowledge, Attitudes, Practice , Humans , Longitudinal Studies , Male , Middle Aged , Patient Compliance/psychology , Quality of Life , Self Efficacy , Sleep Apnea, Obstructive/therapy , Surveys and Questionnaires , Time Factors
6.
Chest ; 144(1): 87-91, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23392731

ABSTRACT

BACKGROUND: Patient cooperation is crucial for the success of noninvasive positive pressure ventilation (NPPV). This study evaluated the efficacy of medical hypnosis to reduce anticipatory anxiety and acclimatization time in children who are candidates for long-term NPPV. METHODS: Medical hypnosis was performed by a trained nurse. The acclimatization time and long-term compliance with NPPV were evaluated. RESULTS: Hypnosis was performed in nine children aged 2 to 15 years. Seven children had a high level of anticipatory anxiety because of a tracheotomy since birth (n=2), a history of maxillofacial surgery (n=2), severe dyspnea because of lung disease (n=2), and morbid obesity and depression (n=1), and two children with obstructive sleep apnea failed standard NPPV initiation. The hypnosis techniques were based on distraction in the youngest patient and indirect or direct hypnotic suggestions in the older children to obtain a progressive psychocorporal relaxation. All patients accepted the interface and the NPPV after the first hypnosis session. A median of three sessions was needed for overnight (>6 h) NPPV acceptance. The 6-month compliance with NPPV was excellent, with a median use of 7.5 h per night. CONCLUSION: Medical hypnosis is an effective, safe, noninvasive, and inexpensive tool for reducing the anticipatory distress and acclimatization time for NPPV. This therapy is particularly useful in children with traumatic experiences, such as a tracheotomy or facial surgical procedures.


Subject(s)
Anxiety/prevention & control , Hypnosis/methods , Patient Compliance/psychology , Positive-Pressure Respiration/psychology , Respiratory Therapy/psychology , Adolescent , Anxiety/psychology , Child , Child, Preschool , Dyspnea/psychology , Female , Humans , Male , Obesity, Morbid/psychology , Pilot Projects , Surgery, Oral/psychology , Tracheotomy/psychology , Treatment Outcome
7.
Rinsho Shinkeigaku ; 50(11): 1026-8, 2010 Nov.
Article in Japanese | MEDLINE | ID: mdl-21921553

ABSTRACT

In March 2009 we sent out the questionnaire to the 4,478 board certified neurologist to ask about the palliative care in ALS. 1,495 anonymous responses (33%) have been returned. 21% of the respondents prescribe morphine, which shows a drastic increase from the 14% in the 2007 survey. However, 77% of them had only less than 5 patients, 47% of them studied and trained themselves. It illustrates that most of the neurologists are not well experienced with morphine, and that they are isolated in practice. However, 47% of the respondents answer that they would prescribe morphine whether or not the national insurance pays. As for the withdrawal of the permanent ventilation, 21% of the respondents were asked by their patients to turn off the ventilation. While 24% of the respondents believe that the withdrawal right not should be promoted, 46% believe that such right should be granted if the decision made by the patient and/or his/her family members can explicitly be recognized. The result illustrates that the physicians are also divided. It may be the time to lay the foundation for the Japanese ALS physicians to discuss openly and candidly together to deal with the wants and wishes of their patients.


Subject(s)
Amyotrophic Lateral Sclerosis/therapy , Neurology , Physicians/psychology , Surveys and Questionnaires , Terminal Care/ethics , Terminal Care/psychology , Conscious Sedation , Family/psychology , Humans , Japan , Morphine/therapeutic use , Positive-Pressure Respiration/psychology , Positive-Pressure Respiration/statistics & numerical data
8.
Curr Opin Pulm Med ; 15(6): 585-90, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19713846

ABSTRACT

PURPOSE OF REVIEW: Positive airway pressure (PAP) therapy is commonly prescribed treatment for obstructive sleep apnea (OSA) in both adults and children. However, the effectiveness of PAP therapy is undermined by poor adherence. The purpose of this review is to improve our understanding of the causes and consequences of nonadherence to PAP therapy and highlight interventions that promote adherence. RECENT FINDINGS: Nonadherence to PAP therapy is associated with higher levels of sleepiness and greater likelihood for cardiovascular morbidity and mortality. Factors consistently associated with nonadherence to PAP therapy include asymptomatic individuals, nasal obstruction, low self-efficacy, lack of risk perception, and lower socioeconomic status. Care by certified specialists and accredited centers may be associated with better adherence but this finding needs to be replicated. Interventions such as cognitive-behavioral therapy, intensive education and support, and reduction of nasal obstruction have been consistently shown to augment adherence to therapy, whereas the benefits of device or interface modifications are less clear. There is a paucity of investigations addressing PAP therapy adherence in children. SUMMARY: Nonadherence limits the effectiveness of PAP therapy in both adults and children. Whereas the causes and consequences of poor adherence to PAP therapy and the ramifications to healthcare delivery are better understood, there remains a dearth of reliable and cost-effective interventions.


Subject(s)
Patient Compliance , Positive-Pressure Respiration , Sleep Apnea, Obstructive/therapy , Adult , Child , Continuous Positive Airway Pressure , Humans , Patient Compliance/psychology , Positive-Pressure Respiration/instrumentation , Positive-Pressure Respiration/methods , Positive-Pressure Respiration/psychology , Sleep Apnea, Obstructive/psychology , Treatment Outcome
9.
South Med J ; 102(6): 589-94, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19434037

ABSTRACT

BACKGROUND: Obstructive sleep apnea-hypopnea syndrome (OSAH) is associated with impairment of cognitive functions and disturbances in emotional status. The aim of this study was to objectively evaluate the benefits of prolonged and sustained treatment for OSAH at two sleep centers serving rural community hospitals. METHODS: Fifty-six patients diagnosed with OSAH syndrome underwent Cognistat, Beck Depression Inventory (BDI) and Millon Behavioral Medicine Diagnostic Inventory (MBMD) testing before initiation of treatment. Repeated testing after six months of therapy with positive airway pressure (PAP) was performed. RESULTS: Significant improvements were noted in the BDI scale scores and a reduction in the MBMD scores reflected initial abnormal clinical personal symptoms that improved with treatment. MBMD analysis showed subjects with fewer symptoms of anxiety post baseline, which were sustained at 6 months post-treatment. Memory function improved as reflected by performance on the Cognistat. Women were observed to have a higher post-treatment BDI and younger patients appeared to have more shifts for improvement than older subjects in depressive symptomatology. CONCLUSIONS: These results indicate that prolonged and sustained PAP therapy is effective in restoring some of the deficiencies in patients with OSAH, particularly in terms of memory, depression, anxiety and increased psychological pathology.


Subject(s)
Cognition , Emotions , Positive-Pressure Respiration/psychology , Sleep Apnea Syndromes/psychology , Adult , Female , Humans , Male , Memory , Middle Aged , Neuropsychological Tests , Psychiatric Status Rating Scales , Sleep Apnea Syndromes/therapy , Surveys and Questionnaires
10.
Ann Fr Anesth Reanim ; 28(3): 215-21, 2009 Mar.
Article in French | MEDLINE | ID: mdl-19278806

ABSTRACT

OBJECTIVES: Non-invasive ventilation (NIV) in patients with acute respiratory failure (ARF) is subject to a large number of failures due to discomfort of the art, the feeling of difficulty breathing and pain. The purpose of this study was to evaluate the efficiency of sophrology to improve conditions for the realization of NIV in patients with ARF. PATIENTS AND METHODS: In this prospective randomized and controlled study, consecutive patients with ARF were included. From the very first NIV session, they received either sophrology during the first 30 min of NIV (S group), or standard care by the same nurse during 30 min (T group). The hemodynamic and ventilatory data were recorded continuously; pain, respiratory difficulty and discomfort were measured with a numeric scale at the end of the session. RESULTS: Thirty patients were included in the study, 27 have been analysed. Each patient received an average of four sessions NIV during the protocol. There was no significant difference between the two groups in terms of improvement in gas exchange. In contrast, there was a significant difference in terms of reduction of difficulty in breathing (-76%), discomfort (-60%) and decrease the pain (-40%) in the sophrology group (p<0.001). Respiratory rate, heart rate and systolic arterial blood pressure were decrease during NIV. CONCLUSION: Sophrology constitutes aid for the achievement of the meetings of NIV in patients' IRA.


Subject(s)
Complementary Therapies/methods , Patient Acceptance of Health Care , Positive-Pressure Respiration/psychology , Respiratory Insufficiency/therapy , Acute Disease , Adult , Aged , Carbon Dioxide/blood , Critical Care/methods , Double-Blind Method , Dyspnea/etiology , Dyspnea/psychology , Dyspnea/therapy , Female , Hemodynamics , Humans , Male , Middle Aged , Oxygen/blood , Pain/etiology , Pain/psychology , Pain Management , Positive-Pressure Respiration/adverse effects , Positive-Pressure Respiration/methods , Positive-Pressure Respiration/nursing , Prospective Studies , Pulmonary Gas Exchange , Respiratory Insufficiency/blood , Respiratory Insufficiency/nursing , Respiratory Insufficiency/psychology
11.
Amyotroph Lateral Scler ; 9(2): 91-8, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18428001

ABSTRACT

Non-invasive ventilation (NIV) is known to improve quality of life and to prolong survival in amyotrophic lateral sclerosis (ALS) patients. However, little is known about the circumstances of dying in ventilated ALS patients. In the light of the debate on legalizing euthanasia it is important to provide empirical data about the process of dying in these patients. In a structured interview, 29 family caregivers of deceased ALS patients were asked about their own and the patient's attitude toward physician-assisted suicide (PAS) and euthanasia, circumstances of dying, and the use of palliative medication. Quantitative and qualitative content analysis was performed on the data. Non-recurring suicidal thoughts were reported by five patients. Three patients and seven relatives had thought about PAS. Seventeen caregivers described the patients' death as "peaceful", while choking was reported in six bulbar patients. In final stages of dying, the general practitioner (GP) was involved in the treatment of 10 patients, with palliative medication including sedatives and opiates being administered in eight cases. In conclusion, in contrast to the Netherlands, where 20% of terminal ALS patients die from PAS or euthanasia, only a small minority of our patients seems to have thought about PAS. The legal situation in Germany (where euthanasia is illegal), a bias due to the selection of NIV patients as well as a high percentage of religious patients and those with good levels of social support from family and friends, might account for this. Most of our patients died peacefully at home from carbon dioxide narcosis, but choking was described in some bulbar patients. Thus, palliative care, especially the use of opiates, anxiolytics and sedatives should be optimized, and the involvement of GP should be strongly encouraged, especially in bulbar patients.


Subject(s)
Amyotrophic Lateral Sclerosis/nursing , Amyotrophic Lateral Sclerosis/psychology , Attitude to Death , Caregivers/psychology , Euthanasia/psychology , Palliative Care/psychology , Positive-Pressure Respiration/psychology , Suicide, Assisted/psychology , Adult , Aged , Female , Germany , Humans , Male , Middle Aged
14.
Klin Padiatr ; 216(1): 16-20, 2004.
Article in German | MEDLINE | ID: mdl-14747965

ABSTRACT

BACKGROUND: Neonate's expression of pain lacks the ability to report pain. Several pain measures exist to assess acute pain in term and preterm neonates. The aim of the present study is to compare them with respect to their validity and reliability. METHOD: Review of the literature and a description of the measures most often cited. Additionally, the validity of the Bernese Pain Scale for Neonates (BPSN) was assessed in a department of neonatology of a university hospital. PATIENTS: Assessments of pain (n = 48) in term and preterm neonates with and without respiratory support. RESULTS: Existing pain measures are using behavioural indicators of pain (eg, facial expression, body posture, movements, and vigilance) as well as physiological indicators of pain (eg, changes in heart rate, respiratory rate, blood pressure, oxygen saturation). The used measures and their feasibility in everyday practice, the study population and the method of validation were presented. The BPSN differentiates pain from nonpain (F = 41.27, p < 0.0001) and the interrater- as well as the intrarater-reliability was high (r = 0.87 - 0.98 and r = 0.98 - 0.99, respectively). CONCLUSIONS: Assessment of acute pain in neonates should take into account the way of validation that has been performed especially with respect to the study population. The BSN is a pain measure with good validity and reliability for the assessment of pain in term and preterm neonates.


Subject(s)
Infant, Newborn/psychology , Infant, Premature/psychology , Pain Measurement/methods , Arousal , Female , Gestational Age , Humans , Infant Behavior , Male , Observer Variation , Pain Measurement/statistics & numerical data , Positive-Pressure Respiration/psychology , Psychometrics/statistics & numerical data , Reproducibility of Results , Switzerland
16.
Chest ; 124(3): 942-7, 2003 Sep.
Article in English | MEDLINE | ID: mdl-12970021

ABSTRACT

OBJECTIVE: Obstructive sleep apnea (OSA) has been shown to affect the quality of life (QOL) in patients, and QOL improves after treatment with nasal continuous positive airway pressure (CPAP). However, the effects on the bed partner of the patient with OSA have received little attention. We studied QOL in patients with OSA and their bed partners, and the effect of CPAP therapy on QOL. DESIGN: Fifty-four patients and their bed partners who had been seen for evaluation of OSA, had undergone polysomnography, and subsequently had received treatment with CPAP. Patients and bed partners completed the Epworth sleepiness scale (ESS) and QOL questionnaires before and after the patients' therapy. SETTING: Sleep disorders center in an academic medical center. PARTICIPANTS: Patients with documented OSA and regular bed partners. INTERVENTIONS: Both individuals completed the 36-item short-form health survey (SF-36), the ESS, and the Calgary sleep apnea quality of life index (SAQLI). At about 6 weeks after CPAP therapy, patients and their bed partners completed the same set of questionnaires again. RESULTS: Of the 54 subjects who completed the study, the mean (+/- SD) apnea-hypopnea index was 48.4 +/- 33.3. For the subjects, the mean ESS decreased from 12.9 +/- 4.4 to 7.3 +/- 4.0 (p < 0.001) after treatment with CPAP. For the bed partners, the mean ESS decreased from 7.4 +/- 6.1 to 5.8 +/- 4.7 (p = 0.02). The mean scores on the SAQLI were 4.1 +/- 1.0 for the subjects and 4.5 +/- 1.3 for the bed partners. Following CPAP therapy, the SAQLI increased in the subjects to 4.9 +/- 1.2 (p < 0.001), and in the bed partners to 5.1 +/- 0.9 (p = 0.002). The SF-36 showed positive changes in both the subjects and the bed partners. Significant improvements were observed in the subjects in role-physical, vitality, social functioning, role-emotional, and mental health domains. In the bed partners, significant changes in the SF-36 were observed in role-physical, vitality, social functioning, and mental health domains. CONCLUSION: OSA results in impaired QOL in both the patients and their bed partners. Treatment with CPAP improves QOL, as measured by the SF-36 and the SAQLI.


Subject(s)
Positive-Pressure Respiration/psychology , Quality of Life/psychology , Sick Role , Sleep Apnea, Obstructive/psychology , Spouses/psychology , Activities of Daily Living/psychology , Adult , Aged , Arizona , Female , Follow-Up Studies , Health Surveys , Humans , Male , Middle Aged , Polysomnography , Sickness Impact Profile , Sleep Apnea, Obstructive/therapy
17.
Intensive Care Med ; 29(4): 615-21, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12618917

ABSTRACT

OBJECTIVE: To collect benchmark data on the MOS 36-Item Short-Form Health Status Survey (SF-36) in patients receiving noninvasive positive pressure ventilation and to examine whether health-related quality of life is influenced by the underlying disease or by physical parameters. DESIGN AND SETTING: Multicentric clinical cross-sectional trial in four general wards specialized in noninvasive positive pressure ventilation. PATIENTS AND PARTICIPANTS: 226 patients (78 chronic obstructive pulmonary disease, 57 kyphoscoliosis, 20 posttuberculosis sequelae, 17 Duchenne muscular dystrophy, 13 polyneuropathy, 13 myopathy, 6 amyotrophic lateral sclerosis, 12 obesity-hypoventilation syndrome, 4 poliomyelitis sequelae, 3 phrenic nerve lesion, 3 central hypoventilation syndrome) who used noninvasive positive pressure ventilation for home mechanical ventilation. MEASUREMENTS AND RESULTS: Health-related quality of life as assessed by the SF-36 was lower than in the general population. Overall the Physical Component Summary (PCS) was significantly lower than the general population norm; the Mental Component Summary (MCS) was also reduced but less markedly. Patients with chronic obstructive pulmonary disease were more impaired in MCS than those with kyphoscoliosis. PCS was significantly associated with age. Gender, lung function, and arterial blood gas values were not significant predictors of health-related quality of life. CONCLUSIONS: Benchmark SF-36 data in patients receiving noninvasive positive pressure ventilation are given. Although physical health is significantly impaired in these patients, this does not necessarily lead to mental limitation, and mental health is influenced by the underlying disease, but not by physical parameters.


Subject(s)
Positive-Pressure Respiration/psychology , Psychometrics , Quality of Life , Analysis of Variance , Cross-Sectional Studies , Female , Health Status Indicators , Home Care Services , Humans , Male , Middle Aged , Surveys and Questionnaires
18.
Dtsch Med Wochenschr ; 127(23): 1245-9, 2002 Jun 07.
Article in German | MEDLINE | ID: mdl-12053282

ABSTRACT

BACKGROUND AND OBJECTIVE: Oral protrusive devices (OPD) are increasingly used in primary snoring and mild-to-moderate obstructive sleep disordered breathing. Due to evidence of reduced compliance with the well established standard treatment of nasal positive airway pressure (CPAP) and reports of patient preference for OPD treatment, particularly in mild cases, OPD may be considered another treatment alternative. PATIENTS AND METHODS: We contacted 192 patients suffering from obstructive sleep breathing disorder, who were treated between May 1996 and September 2001 with an OPD. The patients" use of the device was evaluated, as were any reasons for ceasing to use the device. RESULTS: 105 patients (54.4%) regularly used the appliance after a mean time of 22.7 12.3 month. 21 patients (10.9%) showed no primary compliance and stopped had using the device before the first somnographic follow-up after a mean time of 3.8 months. In this investigation 76 patients (80,2%) were classified as responders and 19 patients (20.8%) as primary non-responders. 22 responders (11.4%) demonstrated no secondary compliance after a mean of 21.9 8.8 months and the discontinued OPD treatment themselves. In 21 patients (10.9%) the nightly respiratory parameters decreased after a mean of 23.0 11.7 months; hence, those patients required CPAP. The cumulative risk using the device after four years as prescribed was 32.2%. We found a correlation between patient compliance, body-mass index and the amount of teeth in the upper and lower jaws. CONCLUSION: OPD compliance seems to be lower than frequently expected. Regular follow-up investigations are necessary to ensure adequate treatment. Poor dental status and an excess body-mass index reduce patient compliance.


Subject(s)
Occlusal Splints , Patient Compliance , Sleep Apnea, Obstructive/rehabilitation , Adult , Aged , Aged, 80 and over , Female , Follow-Up Studies , Humans , Long-Term Care/psychology , Male , Middle Aged , Patient Compliance/psychology , Polysomnography , Positive-Pressure Respiration/psychology , Risk Factors , Sleep Apnea, Obstructive/psychology , Snoring/prevention & control , Snoring/psychology
19.
Am J Respir Crit Care Med ; 164(4): 608-13, 2001 Aug 15.
Article in English | MEDLINE | ID: mdl-11520724

ABSTRACT

Application of continuous positive airway pressure (CPAP) as the standard treatment for sleep apnea/hypopnea syndrome (SAHS) is a moot point. Studies on the effectiveness of this treatment have been challenged because of the lack of a suitable placebo. The recent description of a true placebo (sham CPAP) prompted us to conduct a randomized trial of CPAP or placebo to assess the effectiveness of CPAP in improving SAHS-related symptoms and daytime function in patients with moderate to severe SAHS. Forty-eight patients, stratified in four groups according to severity, were randomly allocated into two treatment groups (optimal and sham CPAP) for a 6-wk period. Of these, 45 completed follow-up (91% males; age: 54 +/- 10 yr; body mass index [BMI]: 32 +/- 6 kg/m(2); apnea-hypopnea index [AHI]: 54 +/- 19 events/h; and Epworth Sleepiness Scale [ESS]: 16 +/- 5). The ESS, a questionnaire on SAHS-related symptoms, Functional Outcomes Sleep Questionnaire (FOSQ), and the Short Form Health Survey (SF-36) were completed at inclusion and after treatment. After 10 d of washout, the placebo group was treated with optimal CPAP and reassessed before and after optimal CPAP. The group receiving optimal CPAP when compared with the group with sham CPAP showed considerably greater improvement in the relief of sleepiness (-9.5 versus -2.3, p < 0.001), other SAHS-related symptoms (-18.5 versus -4.5, p < 0.001), vigilance (+8.5 versus +3.4, p = 0.009), and general productivity (+4.0 versus +0.5, p = 0.04) FOSQ scales. Both groups used a similar number of hours for the optimal and the sham CPAP (4.3 versus 4.5, (p = NS). The patients initially treated with placebo CPAP improved significantly more when optimal CPAP was applied for ESS (-2.3 versus -6.7, p < 0.001) and other sleep apnea syndrome (SAS)-related symptoms (-4.5 versus -11.2, p = 0.02). Our study provides strong evidence of the effectiveness of CPAP treatment in improving symptoms and perceived health status in moderate to severe SAHS.


Subject(s)
Activities of Daily Living , Positive-Pressure Respiration/methods , Sleep Apnea Syndromes/physiopathology , Sleep Apnea Syndromes/therapy , Sleep Stages , Adult , Aged , Attitude to Health , Body Mass Index , Double-Blind Method , Female , Follow-Up Studies , Health Status , Humans , Male , Middle Aged , Obesity/chemically induced , Obesity/complications , Placebos , Positive-Pressure Respiration/psychology , Positive-Pressure Respiration/standards , Severity of Illness Index , Sleep Apnea Syndromes/diagnosis , Sleep Apnea Syndromes/etiology , Smoking/adverse effects , Surveys and Questionnaires , Time Factors , Treatment Outcome
20.
Thorax ; 56(7): 513-8, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11413348

ABSTRACT

BACKGROUND: The sleep apnoea/hypopnoea syndrome (SAHS) causes snoring, apnoeas, and restlessness during sleep which partners frequently complain about. A study was undertaken to determine the impact on partners of SAHS and of treatment of the patient with continuous positive airway pressure (CPAP). METHODS: Forty nine partners and patients with SAHS booked for CPAP treatment completed in house and validated questionnaires (Pittsburgh sleep quality index, Short Form 36 self-reported health status) before the patient started treatment. Twenty three couples in whom the index SAHS patient had no driving problems were recruited to a randomised crossover trial with 1 month limbs of CPAP and placebo capsule. At the end of each limb the partners' sleep was monitored by home polysomnography (PSG) and questionnaires were completed. RESULTS: Before treatment partners frequently reported moderate to severe disturbance from patient snoring/apnoeas/restlessness and had poor sleep quality and self-reported health status. In the crossover study (22 completed) the partners' objective sleep quality did not differ between CPAP and placebo, but they reported benefit from treatment of the patients with CPAP in subjective sleep quality (p=0.05) and disturbance to sleep (p=0.03). The reported change in partners' sleep quality between pre-study and following CPAP treatment correlated positively with CPAP use (r=0.5, p=0.01). CONCLUSIONS: Partners of patients with SAHS have poor sleep quality and self-reported health status but only subjective sleep quality benefits from treatment of the patient with CPAP.


Subject(s)
Positive-Pressure Respiration/psychology , Quality of Life , Sleep Apnea Syndromes/therapy , Spouses , Cross-Over Studies , Data Interpretation, Statistical , Female , Humans , Male , Middle Aged , Polysomnography/methods , Positive-Pressure Respiration/methods , Sleep Apnea Syndromes/diagnosis , Sleep Apnea Syndromes/psychology , Surveys and Questionnaires
SELECTION OF CITATIONS
SEARCH DETAIL
...