Abstract
Background. The prevalence of patients supported with home mechanical ventilation (HMV) for chronic respiratory failure has increased. However, the clinical outcomes associated with HMV are largely unknown. Methods. We performed a systematic review of studies evaluating patients receiving HMV for indications other than obstructive lung disease, reporting at least one clinically relevant outcome including health-related quality of life (HRQL) measured by validated tools; hospitalization requirements; caregiver burden; and health service utilization. We searched MEDLINE, EMBASE, CINAHL, the Cochrane library, clinical trial registries, proceedings from selected scientific meetings, and bibliographies of retrieved citations. Results. We included 1 randomized control trial (RCT) and 25 observational studies of mixed methodological quality involving 4425 patients; neuromuscular disorders (NMD) (); restrictive thoracic diseases (RTD) (); obesity hypoventilation syndrome (OHS) (); and others (). HRQL was generally described as good for HMV users. Mental rather than physical HRQL domains were rated higher, particularly where physical assessment was limited. Hospitalization rates and days in hospital appear to decrease with implementation of HMV. Caregiver burden associated with HMV was generally high; however, it is poorly described. Conclusion. HRQL and need for hospitalization may improve after establishment of HMV. These inferences are based on relatively few studies of marked heterogeneity and variable quality.
1. Introduction
Home mechanical ventilation (HMV) is a viable and effective treatment strategy for patients with chronic respiratory failure and has been associated with a survival benefit [1–3]. Provision of mechanical ventilation outside of an institution has been in effect for more than 50 years, originating during the polio epidemic [4]. In recent decades, the prevalence has increased, with the expanded utilization of HMV for a broad range of neuromuscular disorders (NMD), restrictive thoracic diseases (RTD), and obesity hypoventilation syndrome (OHS). The Eurovent study estimated the prevalence of HMV users at 6.6 per 100,000 population, excluding OHS [1]. In comparison, recent Canadian data has determined that 10.9 per 100,000 population receive HMV [5]. The use of noninvasive ventilation (NIV) in stable chronic obstructive pulmonary disease (COPD) is an area of controversy. This group accounts for approximately one-third of users in Europe; however, given insufficient and often conflicting data current, Canadian guidelines do not support widespread usage in this population.
Health related quality of life (HRQL), constrained hospital resources, and increasing demands for prolonged mechanical ventilation have motivated providers, patients, and families to create a sustainable home environment for ventilatory assisted individuals (VAIs). While clinical practice guidelines to standardize the management of HMV have been developed, their implementation is uncertain [4]. This likely relates in part to variability in resource availability, inconsistent follow-up, clinician preference, and limited available scientific evidence [5].
While survival is indeed an important long-term outcome, use of HMV should also focus on additional patient-centered and system-level outcomes including HRQL, hospitalization needs, health resource utilization, and the role of caregivers. We therefore conducted a systematic review of the literature to examine all available studies evaluating at least one clinically relevant patient-centered and health resource utilization outcome in patients receiving HMV.
2. Methods
2.1. Search Strategy
A comprehensive search of MEDLINE, EMBASE, CINAHL, and the Cochrane library (1996 to August 2013) was performed with an experienced librarian (see Supplementary Methods in Supplementary Material available online at http://dx.doi.org/10.1155/2016/6547180). Three comprehensive search themes were derived and combined using the Boolean operator “AND”. The first theme included keyword/MESH headings related to disease states associated with chronic respiratory failure (CRF). The second theme was treatment related and included terms pertaining to all forms of mechanical ventilation. The third theme identified the setting of interest, this being a noninstitutional home environment. There were no restrictions on study design, language, or patient age. Studies published prior to 1996 were excluded to reflect important advances in home ventilator technology and patient management. In addition, we searched the abstracts from key scientific proceedings (CHEST, American Thoracic Society and European Respiratory Society, 2010–2013), the bibliographies of all retrieved articles and recent reviews, and clinical trials registries. Lastly content experts were contacted to locate additional sources of unpublished data that may be appropriate to our evidence synthesis.
2.2. Study Selection
Two trained reviewers (Erika J. MacIntyre and Leyla Asadi) independently conducted an initial eligibility screen of all retrieved titles and abstracts. Studies were selected for full text review if they met the following criteria: (1) study design (original research, other than case reports); (2) population (cohorts with CRF; studies examining COPD exclusively were not included as the use of HMV in stable COPD is currently not recommended in Canada); (3) intervention (invasive tracheostomy ventilation (TV) or NIV); (4) setting (noninstitutionalized residence); and (5) outcomes (patient- and/or family-centered outcomes other than survival and measures of health resource utilization; physiologic measures including blood gases and pulmonary function were not considered patient-centered; initial screening was broad and selection subsequently narrowed to our specific outcomes of interest).
2.3. Data Collection
Full text review, data extraction, and methodological quality scoring were independently performed by the same two reviewers on standardized data collection forms for studies that met inclusion criteria. Disagreements between reviewers were resolved through discussion and if consensus could not be achieved, discrepancies were resolved by a third reviewer (S.M.B.).
2.4. Methodological Quality Assessment
Methodological quality was scored using a modified version of the Downs and Black checklist (see Supplementary Methods) [31]. The original checklist contains 27 items; however, 10 items pertaining to interventional trials were excluded as only a single interventional trial was identified. In addition, the question of power was changed to whether the study commented on power and disclosure/conflict of interests was added. In the end, studies were scored by the following subscales: reporting [7], external validity [2], bias [5], confounding [3], and disclosure [1] for a total score range of 0 (poor quality) to 19 (rigorous).
2.5. Outcomes
All patient- and family-centered outcomes and health resource outcomes for this systematic review were determined a priori. Our primary outcomes included health related quality of life (HRQL) measured quantitatively by a validated HRQL assessment tool and hospitalization rates including number of admissions and days in hospital. Secondary outcomes consisted of family caregiver (FCG) burden defined by use of standardized or validated questionnaires, HRQL assessment tools or structured interviews grouped by domain, and health service utilization (including any interaction with a physician, allied health professional, or clinical test). Cost implications to either the system or families, sleep quality assessed by quantitative measures, and incidence of decannulation were also considered important secondary outcomes.
3. Results
3.1. Study Characteristics
The database search generated 1371 citations, of which 36 met inclusion criteria. An additional 6 articles, identified through other sources, were included in the full text review for a total of 42 articles. German language articles () were screened for content by one reviewer (Erika J. MacIntyre) and a professional translator (Regina Landeck). Reasons for exclusion are shown in Figure 1.
After screening, we included 1 randomized control trial (RCT) [3] and 25 observational studies (before and after, [6–15]; cohort, [16–18]; cross-sectional surveys, [19–22, 24–29, 32]; descriptive, [30]) (Table 1).
3.2. Patient Characteristics
A total of 4425 patients were studied. There were three broad disease states contributing to CRF and establishment of HMV: NMD (patients, ); RTD (); OHS (). One study did not provide the number of patients in each disease category (). The remainder were classified as “other,” defined as a mixture of patients including many with COPD () (Table 2). NIV was used in the majority (85%) of patients ().
3.3. Methodological Quality Assessment
Overall quality was variable (Table 1). Scores ranged from 4 for the descriptive study to 18 for the RCT out of 19 (see Supplementary Results). Median scores were 14 for before and after studies (range 8–17), 17 for cohorts [13–16], and 10 for cross-sectional surveys [5–14, 31]. The greatest deficiencies across studies were in the categories of confounding (median score 1 out of 3) and disclosure (reported in only 6 studies).
3.4. Health Related Quality of Life
Eleven studies provided data on HRQL using one or more general or disease-specific tools, including the Short Form-36 (SF-36), Sickness Impact Profile (SIP), Severe Respiratory Insufficiency (SRI) questionnaire, Profile of Mood States (POEMS), Munich Quality of Life Dimensions (MLDL), Health Index (HI), Sense of Coherence (SOC) scale, Saint George Respiratory Questionnaire (SGRQ), and the Chronic Respiratory Disease Questionnaire (CRQ) (see Supplementary Results) [3, 6–8, 11–13, 17, 22, 25, 26].
HRQL was generally described as good. Five studies examined HRQL before and after HMV using the SF-36 [3, 6, 7, 12, 13]. Table 3 presents statistically significant changes by item.
Improved HRQL was more consistent across the mental compared to the physical domains. With respect to mental capacity scores, every study examining OHS or RTD reported improvement in at least one domain or summary score following the establishment of HMV. There was no evidence of a clinically important deterioration in any group. Physical component scores were more heterogeneous. In NMD, one study found deterioration in the domain of physical functioning and improvement only seen in the item of general health in a single study; otherwise there was no change. The majority of the studies examining the remaining disease states reported benefit in at least one physical domain and/or overall physical component score.
The remaining 6 studies were of mixed design and applied different HRQL tools [7, 11, 17, 22, 25]. Several of these compared HRQL between disease states with conflicting results [7]. Using the SIP instrument, Markström et al. found significant functional impairment (score of >10%) in NMD () compared to no clinical dysfunction in RTD (score of <5%) (), while Dellborg et al. noted comparable improvement in both NMD () and RTD () [8, 26].
3.5. Hospitalization
Nine studies (36%) examined hospitalization rates following the institution of HMV (patients, ) [6, 7, 9–12, 14, 20, 32]. Results are presented in Table 4, omitting one study which did not present admission rates immediately following HMV establishment [20]. In general, the initial titration took place in hospital. Hospitalization rates and days in hospital overall appear to be low and to decrease in subsequent years across studies and disease states following the implementation of HMV. Reasons for admission were related predominately to cardiac or respiratory related problems where specified [7, 10, 11, 14]. Admissions for ventilator setting adjustments or equipment servicing were infrequent and generally not considered. Interpretation of study findings is limited and could not be quantitatively pooled due to heterogeneity across diseases and reporting methods [6, 11, 32]. One study found hospitalization rates to be one of the strongest predictors of impaired HRQL [22].
3.6. Secondary Outcomes
Family caregiver (FCG) characteristics are presented in Table 5 (studies, ; caregivers, ) [18, 19, 21, 24, 25, 28, 29]. FCGs of TV users were predominantly examined (NIV use 45% versus 85% when all studies were examined). FCGs were younger than HMV users, predominantly female (76%) and of spousal (54%) or parental (31%) relation. Fewer than half were actively employed and many described having to quit work or reduce work hours to enable care for VAIs. Given the choice, 80% of FCGs would choose HMV again for their loved ones. This number is higher (88%) in studies that examined caregivers of NMD and RTD patients only compared to the study that included caregivers of a mixed cohort (42%) [19, 25, 27, 29]. Parental caregivers also appeared to have a greater sense of satisfaction with their decision [18, 19, 27]. Some attempted to quantify burden using a variety of tools including the Family Burden Questionnaire, the Zarit interview, and the caregiver burden inventory. All studies highlighted burden in the domains of financial strain, negative impact on employment, and insufficient time for oneself and for personal relationships [19, 21, 24].
Health resource use and the economic impact of HMV, beyond hospitalization, were assessed in 7 studies [16, 20, 23, 25, 28–30, 32]. Access to medical experts, phone calls to a unit specializing in HMV, ventilator servicing, home visits by technicians or nursing staff, and education were identified as important resources [16, 20, 32]. Cost was high and home care appeared to be the largest expense. Despite most patients having some level of health insurance coverage, many families suffered out-of-pocket expenses either in the form of lost wages or in order to privately fund home care, medications, or equipment. Crude cost estimates are provided in Table 6. Despite this, Moss et al. observed significantly less cost with home compared to institutionalized VAIs [29].
All studies presenting data on sleep quality documented improvements in either overall sleep quality or sleep related symptoms including morning headaches, nocturnal dyspnea, and daytime somnolence with HMV [3, 8, 10]. No study discussed decannulation in an ambulatory setting.
4. Discussion
In our scoping review we identified 26 unique studies reporting data on at least one patient-centered outcome other than survival in 4425 HMV users.
4.1. Summary of Major Findings
We found that HMV generally had a favorable impact on HRQL. Not surprisingly, improvement was more prominent and consistent for mental domains compared with physical domains across HRQL measures, particularly in those with NMD. We found HMV may be associated with an initially low and a subsequently reduced rate of hospitalization and days in hospital following implementation. While poorly described, FCG burden appears quite high. This likely relates in part to the financial strain associated with keeping VAIs in a home environment and may contribute to the unwillingness of some caregivers to choose HMV for their loved one again if given a second opportunity.
4.2. Context with Previous Studies
We believe our findings require thoughtful interpretation given that they are based on relatively few studies of mixed design and methodological quality describing small cohorts of heterogeneous patients. In general, pooled quantitative analyses could not be performed due to heterogeneity across studies, particularly in terms of the measures of HRQL, hospitalization requirements and caregiver burden that were applied. In addition, our findings are also likely confounded by concomitant cointerventions associated with entry into a multidisciplinary HMV program, such as improved medical attention, education, airway clearance strategies, home care, and provision of mobility aids [4, 33, 34]. With the exception of one study, HMV was offered to all individuals with CRF and as such, there were no proper controls for comparison. However, the natural history of many of these chronic incurable diseases includes progressive decline in health status with an expected increased health resource use which was not seen.
For NMD, there are plausible reasons for the lack of improvement in HRQL association with initiation of HMV. First, many NMD are progressive and can be associated with rapid clinical deterioration. In ALS, HRQL is generally worse in those with bulbar muscle dysfunction and HMV may be of limited benefit [3]. Second, ten physical component items in the SF-36 assess the ability to perform physical tasks, which may not be possible for patients with advanced NMD. The SRI instrument may address some of these shortcomings and appears to be a more sensitive HRQL assessment tool in HMV users [35].
We also examined several clinically important secondary outcomes. Family care givers were often younger, female, and of spousal or parental relation. Most FCGs were caring for loved ones receiving TV, suggesting a greater burden associated with invasive ventilation. Importantly, nearly one-fifth of all FCGs would not choose the option of HMV again, if given the opportunity, suggesting that the perceived burden is unmanageably high for many. It would seem that there are differences in caregiver perceptions of burden across disease states with burden being the least in caregivers of patients with NMD and RTD, particularly in the case of parents, slightly higher in ALS where the FCG is more often a spouse, and highest in caregivers of mixed cohorts. Moreover, these studies reinforce that FCG burden for HMV patients is poorly evaluated and understood.
There is limited data on the health economic implications of HMV; however, we can make several observations. There appears to be wide variation in the policies, procedures, and patterns of practice around the assessment, initiation, and maintenance of patients on HMV across health jurisdictions. Ambulatory service provision is necessary to maintain patients in a home environment, but this is currently not standardized. Some centers have specialized multidisciplinary home ventilation units that follow all VAIs, whereas in others follow-up can be infrequent and may not even involve a physician. The costs of maintaining VAIs at home are high; however, this is likely significantly less than the cost of long-term institutionalization. Many FCG suffered out-of pocket expenses and financial strain was highlighted in all 8 studies where caregiver burden was examined. This would strongly suggest that the current level of home support is inadequate.
No studies reported on decannulation. This is likely due to the following: (1) NIV use became the preferred first-line method of HMV by patients and providers for which weaning may be less relevant compared with invasive TV. Moreover, elective “ramping” of up to 24 hours of NIV may often obviate the need for invasive TV; (2) HMV patients are referred from chronic ventilation units where patients may have already failed to wean; and (3) in many patients, respiratory recovery is unlikely.
4.3. Strengths and Limitations
A prior systematic review aimed to evaluate the impact of HMV on hospitalization and sleep quality in NMD and RTD; however, the paucity of data limited the capacity for clear inferences [2]. In addition, a recent systematic review evaluated the impact of NIV on patient reported outcomes in a similar population. Their conclusions regarding HRQL were largely coherent with our findings; however, there was no assessment of the impact of NIV on hospitalizations, health resource implications, or FCG burden [36]. Our review has overcome some of these limitations by using a broader search strategy [37]. We believe our findings, based on a larger body of literature, better represent the impact of HMV on patient-centered outcomes beyond survival.
Our study also has notable limitations. Firstly, small sample size, heterogenous study design, and variable methodological quality weaken the strength of inferences from our study. Secondly, our outcomes may have been influenced by methods of ventilation and compliance. Compliance is generally considered use for >4 hours/night, 5 nights/week, and while this was an item in our assessment of methodological quality, duration and usage were not fully taken into consideration. Thirdly, many of our outcomes were prone to bias, particularly survivorship bias. Fourthly, not all relevant patient-centered outcomes were considered and we acknowledge that not all outcomes are of equal value to patients and/or FCGs. Fifthly, there is heterogeneity within disease categories and our findings may not be applicable across all specific disease states. Lastly, as previously stated, concomitant cointerventions associated with entry into a multidisciplinary program confound and may exaggerate the beneficial effects of HMV.
4.4. Clinical and Health Policy Implications
The utilization of prolonged mechanical ventilation in CRF secondary to NMD, RTD, and OHS is increasing and likely represents a significant escalation in the complexity and cost of home care. Uncertainty surrounding optimal HMV service provision on patient-centered outcomes is an important knowledge gap and lack of evidence undoubtedly contributes to wide variation in clinical practice, including patterns of home ventilation initiation and titration, which may incur considerable costs to the health system. A large RCT evaluating HMV versus a nonventilated control would be challenging and perhaps unethical. We therefore will need to rely on high quality observational data and randomized trials of selected processes of care to further our understanding of the ideal method of HMV to optimize patient-centered outcomes. Then resources can be appropriately allocated by policy makers and providers along with a greater homogenization of standard practices to ensure high quality care is delivered to patients and their families.
5. Conclusion
In summary, our systematic review suggests that HMV likely provides quality of life benefit and reduced hospitalizations in patients with CRF secondary to NMD, RTD, and OHS. However, small sample sizes, heterogeneity in study design, and variable methodological quality weaken these inferences. With the preferential and proactive implementation of noninvasive over invasive ventilation, the utilization of HMV is likely to expand considerably. Future investigations are clearly needed to better understand the optimal methods for providing care for HMV patients, along with associated caregiver concerns and health economic implications.
Abbreviations
| HMV: | Home mechanical ventilation |
| NIV: | Noninvasive ventilation |
| TV: | Tracheostomy ventilation |
| CRF: | Chronic respiratory failure |
| BPAP: | Bilevel positive airway pressure |
| VAI: | Ventilator assisted individual |
| COPD: | Chronic obstructive pulmonary disease |
| NMD: | Neuromuscular disorders |
| RTD: | Restrictive thoracic disease |
| OHS: | Obesity hypoventilation syndrome |
| HRQL: | Health related quality of life |
| FCG: | Family caregiver |
| SF-36: | Short Form-36 |
| SIP: | Sickness Impact Profile |
| SRI: | Severe Respiratory Insufficiency questionnaire |
| RCT: | Randomized control trial. |
Disclosure
Sean M. Bagshaw holds a Canada Research Chair in Critical Care Nephrology and is a Clinical Investigator supported by Alberta Innovates-Health Solutions (AI-HS).
Competing Interests
The authors declare that no potential competing interests exist with any companies/organizations whose products or services may be discussed in this paper.
Authors’ Contributions
Sean M. Bagshaw and Erika J. MacIntyre had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Erika J. MacIntyre contributed to the study design, literature search, retrieval of studies, data extraction, study quality assessment, and drafting of the paper. Leyla Asadi contributed to the retrieval of studies and study quality assessment. Doug A. Mckim contributed to the study design and drafting of the paper. Sean M. Bagshaw contributed to the study design, data extraction, study coordination, and drafting of the paper.
Acknowledgments
Regina Landeck, a certified member of the Association of Translators and Interpreters of Alberta, provided translational services for German articles to English. Elizabeth Dennet, an experienced librarian with the University of Alberta, provided assistance with development of the search strategy and the literature search. Dr. Bagshaw is supported by Canada Research Chair in Critical Care Nephrology and an Independent Investigator Award from Alberta Innovates-Health Solutions.
Supplementary Materials
Supplementary material contains the literature search strategy, the modified Down’s and Black study quality assessment, a detailed list of disease states and a brief explanation of the health related quality of life and caregiver assessment tools that were used.