| Literature DB >> 32947851 |
Anna Brugnolli1, Federica Canzan2, Luigina Mortari3, Luisa Saiani2, Elisa Ambrosi2, Martina Debiasi1.
Abstract
This review assesses the effectiveness of interventions to reduce physical restraint (PR) use in older people living in nursing homes or residential care facilities. A systematic search of studies published in four electronic databases (MEDLINE, CINHAL, PsycINFO, Cochrane Central Register of Controlled Trials). The review included individual and cluster randomized controlled trials that compared educational training and multicomponent programs to avoid PR use. Risk bias of randomized controlled trials (RCTs) was assessed according to the Cochrane Handbook for Systematic Reviews of Interventions. This review includes 16 studies in a qualitative synthesis that met the inclusion criteria, nine of them offered a multicomponent program and seven offered only educational training. The results of the 12 studies included in the meta-analysis showed a significant trend in favor of intervention over time and intensity of PR use tends to decrease. The review indicates that educational programs and other supplementary interventions should be effective, but the heterogeneous operative definition of physical restraints can make difficult data generalization.Entities:
Keywords: meta-analysis; nursing homes; older people; physical restraint; systematic review
Mesh:
Year: 2020 PMID: 32947851 PMCID: PMC7558973 DOI: 10.3390/ijerph17186738
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 3.390
Figure 1PRISMA Flow Diagram.
Characteristics of included studies.
| Authors (Year) Study Design [Ref] | Country Setting | Sample | Interventions | Control | Follow-Up Period | Primary and Secondary Outcome | |||
|---|---|---|---|---|---|---|---|---|---|
| Education Training | Consultation (APN) and Guidance | Change Policy Implementation Guideline | Availability Alternative Intervention | ||||||
| Germany | ✓ | ✓ | ✓ | Usual care | 6–12 months | Physical restraint use | |||
| USA | ✓ | Usual care | 1–12 months | Side rail use | |||||
| USA | ✓ | ✓ | Usual care | 6–9–12 months | Physical restraint use | ||||
| Netherlands | ✓ | ✓ | ✓ | ✓ | Usual care | 4–8 months | Belt restraint use | ||
| Netherlands | ✓ | ✓ | ✓ | ✓ | Usual Care | 4–8 months | Belt restraints use e | ||
| Netherlands | ✓ | ✓ | ✓ | ✓ | Usual care | 24 months | belt restraints use | ||
| Netherlands | ✓ | ✓ | Usual care | 1 month | Physical restraint use | ||||
| Dutch | ✓ | ✓ | Usual Care | 1–4–8 months | Physical restraint status, intensity | ||||
| Dutch | ✓ | ✓ | Usual Care | 1–4–8 months | Physical restraint status, intensity | ||||
| Germany | ✓ | ✓ | ✓ | Usual care | 3 months | ||||
| Germany | ✓ | ✓ | Standard information | 3–6 months | |||||
| Sweden | ✓ | Usual care | 6 months | ||||||
| Baltimore (USA) | ✓ | Usual care | 6 months | ||||||
| Norway | ✓ | Usual care | 7 months | ||||||
| Norway | ✓ | Usual care | 6–12 months | ||||||
| Norway | ✓ | Usual care | 7 months | ||||||
N = number of residents recruited at baseline; Complete data = residents at study endpoint; NH = nursing home; IG = intervention group; CG = control group.
Figure 2Risk of bias summary.
Figure 3Risk of bias graph: review authors’ judgements about each risk of bias item presented as percentages across all included studies.
Results of included studies.
| Author (Year) [Ref] | MA * | Results on Physical Restraint Use | Results on Fall Rate–Fall-Related Injuries |
|---|---|---|---|
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| Change in any physical restraint prevalence from baseline to follow-up | ≥1 Fall 12 months | |
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| Side rail use immediately post (1 month) e 12 months | Fall rate 12 months | |
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| Prevalence restraint use (Individual as units of analysis) | Fall rate | |
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| At least one physical restraint device | Falls | |
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| At least one physical restraint device | Falls | |
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| At least one physical restraint 24 months | ||
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| Restraint use (prevalence) | ||
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| Change in restrain status | ||
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| Not restrained vs. restraint | ||
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| 100% not restrained (free) 3 months | Falls 3 months | |
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| Any physical restraint | Residents ≥1 fall during period study | |
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| Physical restraint 6 months | Falls 6 months | |
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| Physical restraint 6 months | ||
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| Frequency of use of restraint–mean (range) | ||
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| Structural restraint | ||
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| Change in any physical restraint physical restraint prevalence from baseline to /7months |
* MA, meta-analysis; Y, yes: studies included in meta-analysis; N, Not included; CG, control group; IC, intervention group; RE, educational rehabilitation; REC, educational rehabilitation with consultation.
Figure 4(a) Effect of educational program at endpoint study on reducing PR use; (b) Effect of educational program at different follow-up on reducing PR use.
Figure 5(a) Effect of a multicomponent program at endpoint study on reducing PR use; (b) Effect of a multicomponent program at different follow-up on reducing PR use.
Search strategy.
| Research Question | Elements of PICOS | Keywords |
|---|---|---|
| P | Restrained residents in nursing home | Residents in nursing home /Long term setting, residential care facilities |
| I | Educational or multicomponent program | Educational training or multicomponent program |
| C | Usual care | |
| O | Status of physical restraint | Physical restraints or coercion |
| S | Experimental studies | Randomized controlled trials, clinical trials, quasi experimental studies |
Risk of bias of included studies.
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| Random sequence generation (selection bias) | Low risk | One cluster was inadvertently allocated to another group as randomized but a sensitivity-analysis of the primary outcomes showed comparable results and we did not expect that this introduced a risk of bias. |
| Allocation concealment (selection bias) | Low risk | Clusters were randomly assigned to study groups by a person affiliated to the study center in Hamburg, but not involved in the study, using a computer-generated randomization list stratified by region with blocks of six, nine, and twelve nursing homes (generated by an independent external biometrician (BH)). One cluster at the study center Halle (Saale) that had been randomized to intervention group 1 was erroneously allocated to the control group due to miscommunication. |
| Blinding of participants and personnel (performance bias) | High risk | Not possible |
| Blinding of outcome assessment (detection bias) | Low risk | […] raters blinded to group allocation. Raters were trained using a standardized list of measures to be rated as physical restraints. We assessed blinding of research assistants at T2 with 53.7% (95% CI, 45.5 to 63.6) of correct ratings indicating successful blinding |
| Incomplete outcome data (attrition bias) | Low risk | |
| Selective reporting (reporting bias) | Low risk | |
| Recruitment bias | Low risk | Recruitment lasted from February to November 2015. All residents that were present in the nursing home on the day of data collection were included. Residents newly admitted during follow-up were also included |
| Baseline imbalance | Low risk | |
| Loss of cluster | Low risk | The interventions were implemented as planned with excep- tion of the one cluster discussed above. |
| Incorrect analysis | Low risk | |
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| Random sequence generation (selection bias) | High risk | “Interventions were randomized to site using the sealed envelope technique” |
| Allocation concealment (selection bias) | High risk | Not done |
| Blinding of participants and personnel (performance bias) | High risk | Blinding of participants was not possible. Personnel were not blinded |
| Blinding of outcome assessment (detection bias) | Low risk | “Observer nurses were unaware of the exact study design, interventions, |
| Incomplete outcome data (attrition bias) | Unclear risk | Not reported flow of study design and participants |
| Selective reporting (reporting bias) | Low risk | Reports included results both primary and secondary outcomes. |
| Recruitment bias | low risk | |
| Baseline imbalance | high risk | statistically significant differences in baseline characteristics emerged concerning the prevalence of PR and the dependency level of participants |
| Loss of cluster | Low risk | no loss of cluster |
| Incorrect analysis | high risk | |
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| Random sequence generation (selection bias) | Low risk | Done “wards were assigned at random to either educational intervention (3 wards) or control status (2 wards) |
| Allocation concealment (selection bias) | Unclear risk | Not reported method of concealment |
| Blinding of participants and personnel (performance bias) | High risk | Blinding of participants was not possible. Personnel were not blinded |
| Blinding of outcome assessment (detection bias) | Low risk | “The observers (two nurses, one occupational therapist and one member of management) were not told to the exact design of the study, the intervention and the division into experimental and control wards” |
| Incomplete outcome data (attrition bias) | Low risk | During the study there were newly admitted patients both in control and intervention group. Dropped out 19 residents, new admitted 18 residents |
| Selective reporting (reporting bias) | Low risk | Reports included results both primary and secondary outcomes. |
| Recruitment bias | Low risk | The wards were assigned at random to either educational intervention or control |
| Baseline imbalance | Low risk | baseline characteristics are quite similar, excepted in depression (statistically significant difference) |
| Loss of cluster | Low risk | no loss of cluster |
| Incorrect analysis | Low risk | Descriptive statistics were computed for the characteristics of the residents. Logistic regression analysis was used to compare restraint use post-intervention, controlling for characteristics of residents |
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| Random sequence generation (selection bias) | Low risk | Not report methods of randomization |
| Allocation concealment (selection bias) | Unclear risk | Not reported method of concealment |
| Blinding of participants and personnel (performance bias) | High risk | Blinding of participants was not possible. Personnel were not blinded |
| Blinding of outcome assessment (detection bias) | Low risk | Trained observers (n511) blinded to the experimental and control conditions measured the use of physical restraints |
| Incomplete outcome data (attrition bias) | Low risk | During the study, 130 dropped out, mainly because of death (75%). The dropout rate includes that of one ward (n = 529 residents) whose staff was unable to attend the educational intervention because of lack of time. |
| Selective reporting (reporting bias) | Low risk | Reports included results both primary and secondary outcomes. |
| Recruitment bias | Low risk | The wards were assigned at random to either educational intervention or control |
| Baseline imbalance | low risk | Baseline characteristic comparisons between residents who completed all four measurements and dropouts showed that these groups differed on most characteristics and is not use stratified or pair matched randomization |
| Loss of cluster | Unclear | One out of 15 clusters was lost to follow-up |
| Incorrect analysis | high risk | |
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| Random sequence generation (selection bias) | Low risk | The 14 psycho-geriatric nursing home wards were randomly assigned to (..) |
| Allocation concealment (selection bias) | Unclear risk | Not reported method of concealment in report and protocol n. ISRCTN10117742. |
| Blinding of participants and personnel (performance bias) | High risk | Blinding of participants was not possible. Personnel were not blinded |
| Blinding of outcome assessment (detection bias) | Low risk | The observers were blinded to the experimental and control conditions. To measure the inter rater reliability, two of the eight observers were selected and they scored the same residents with restraints (k = 1.0). |
| Incomplete outcome data (attrition bias) | Low risk | 33 residents were not included in the analyses, mainly because these residents died or informed consent had not been obtained. A total of 105 residents were included in the analyses. |
| Selective reporting (reporting bias) | Low risk | Reports included results both primary and secondary outcomes. |
| Recruitment bias | low risk | nursing home wards were randomly assigned to either educational intervention or control status. |
| Baseline imbalance | low risk | Not use stratified or pair matched randomization |
| Loss of cluster | unclear | “The study was part of a larger study focusing on the use of physical restraints on psychogeriatric |
| Incorrect analysis | high risk | |
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| Random sequence generation (selection bias) | Low risk | Despite the randomization, there were differences in baseline characteristics of participants between the two groups. |
| Allocation concealment (selection bias) | Low risk | An independent organization performed randomization according to nursing home after baseline assessment of all restrained residents. |
| Blinding of participants and personnel (performance bias) | High risk | Blinding of participants was not possible. Personnel were not blinded |
| Blinding of outcome assessment (detection bias) | High risk | Not done: “Data collection was, therefore, unblended” |
| Incomplete outcome data (attrition bias) | Low risk | Drop out 52 GI (19.4%), 30 GC (18.5%) |
| Selective reporting (reporting bias) | Low risk | Reports included results both primary and secondary outcomes. |
| Recruitment bias | Low risk | Individual were not recruited after randomized cluster |
| Baseline imbalance | High risk | “Despite the randomization, there were differences in baseline characteristics of participants between the two groups. The sex ratio was unbalanced, and the number of restrained residents differed between the IG and the CG” |
| Loss of cluster | Low risk | No loss of cluster during study |
| Incorrect analysis | low risk | Before definitive analyses, potential cluster effects were estimated for all models. For all analyses, cluster (nursing home) effects of nursing homes accounted for approximately 1.5% of the total variance and individual effects for more than 98%, so clusters were not considered in the final analysis. |
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| Random sequence generation (selection bias) | Low risk | Computer generated randomization lists will be used for allocation of clusters in blocks of four, six and eight nursing homes. Randomization will be stratified by region |
| Allocation concealment (selection bias) | Low risk | Paper and Protocol ISRCTN 34974819: “Clusters will be allocated after collection of baseline and prevalence data by an external researcher, not involved in the study. The external researcher informs each cluster about its group assignment |
| Blinding of participants and personnel (performance bias) | High risk | Blinding of participants was not possible. Personnel were not blinded |
| Blinding of outcome assessment (detection bias) | Low risk | The primary outcome of this study is obtained by trined external investigators. |
| Incomplete outcome data (attrition bias) | Low risk | No nursing home dropped from the study |
| Selective reporting (reporting bias) | Low risk | Reports included results both primary and secondary outcomes like in Protocol. |
| Recruitment bias | low risk | Newly admitted patients in cluster during study, but individuals were not informed about the intervention or control group. |
| Baseline imbalance | Low risk | Randomized stratification |
| Loss of cluster | Low risk | No loss of cluster |
| Incorrect analysis | Low risk | Cluster adjusted 95% confidence intervals of prevalence data were estimated corresponding to the cluster size weighted prevalence estimation from cluster means taking into account variance of cluster means. |
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| Random sequence generation (selection bias) | Low risk | “The randomization was based on a lottery system using identification codes” |
| Allocation concealment (selection bias) | High risk | Not done |
| Blinding of participants and personnel (performance bias) | High risk | Blinding of participants was not possible. Personnel were not blinded |
| Blinding of outcome assessment (detection bias) | High risk | Not done |
| Incomplete outcome data (attrition bias) | low risk | |
| Selective reporting (reporting bias) | Low risk | Reports included results both primary and secondary outcomes. |
| Recruitment bias | Low risk | |
| Baseline imbalance | unclear | At baseline, only age, sex, and wandering behavior differed between the groups, whereas at follow-up age, sex, and cognitive level were all significantly different. |
| Loss of cluster | Low risk | No loss of cluster |
| Incorrect analysis | Low risk | The difference between IG and CG was analyzed by incorporating potential confounders into a multiple logistic regression analyses with a backward selection algorithm and adjusted for the cluster effect |
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| Random sequence generation (selection bias) | Low risk | Done “The allocation procedure was a fixed, uniform randomization scheme by computer algorithm”. |
| Allocation concealment (selection bias) | Unclear risk | Unclear |
| Blinding of participants and personnel (performance bias) | High risk | Not blinding |
| Blinding of outcome assessment (detection bias) | High risk | Not blind “nursing staff (nonblind) reported two or more behaviors on the PGDRS that were |
| Incomplete outcome data (attrition bias) | Low risk | |
| Selective reporting (reporting bias) | Low risk | Report included primary and secondary outcomes. |
| Recruitment bias | Low risk | |
| Baseline imbalance | Low risk | no difference except for number of females in the intervention group |
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| Random sequence generation (selection bias) | Low risk | The nursing homes were randomly assigned to the treatment intervention or control condition, two in each group, after stratification for size. |
| Allocation concealment (selection bias) | Unclear risk | Not reported in paper |
| Blinding of participants and personnel (performance bias) | High risk | Blinding of participants was not possible. Personnel were not blinded |
| Blinding of outcome assessment (detection bias) | Low risk | Data were collected immediately before and after the intervention period by a trained rater who was blind to the study hypothesis and to treatment allocation. |
| Incomplete outcome data (attrition bias) | low risk | Drop out only 9 patient in control group for death |
| Selective reporting (reporting bias) | Low risk | Reports included results both primary and secondary outcomes. |
| Recruitment bias | Unclear | unclear methods. Not report CONSORT flow diagram |
| Baseline imbalance | Low risk | At baseline, the number of restraint and BARS scores did not differ between the groups |
| Loss of cluster | Low risk | No loss of cluster |
| Incorrect analysis | high risk | |
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| Random sequence generation (selection bias) | Unclear | Not described |
| Allocation concealment (selection bias) | Unclear | Not reported in paper |
| Blinding of participants and personnel (performance bias) | High risk | Blinding of participants was not possible. Personnel were not blinded |
| Blinding of outcome assessment (detection bias) | Low risk | “The administration of the outcome measures and drug recording were done by a trained research nurse who was uninformed” |
| Incomplete outcome data (attrition bias) | High risk | Drop out 61.1% in intervention group and 53.1% in usual care group. |
| Selective reporting (reporting bias) | Low risk | Reports included results both primary and secondary outcomes. |
| Recruitment bias | unclear | not described |
| Baseline imbalance | high risk | “were differences in proportion of using physical restraint, antipsychotics, and total CMAI score between the groups”. |
| Loss of cluster | low risk | |
| Incorrect analysis | high risk | |
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| Random sequence generation (selection bias) | Low risk | Done “All homes in the geographical area were invited to participate following a list in randomized Order” |
| Allocation concealment (selection bias) | unclear risk | Not reported in paper and in protocol Clinical Trials NCT01715506 |
| Blinding of participants and personnel (performance bias) | High risk | Blinding of participants was not possible. Personnel were not blinded |
| Blinding of outcome assessment (detection bias) | Low risk | “All data in the 24 care homes were collected within 1 week by research assistants blind to the study |
| Incomplete outcome data (attrition bias) | High risk | Dropout from baseline to follow-up was 35 (30%) in the intervention group and |
| Selective reporting (reporting bias) | Low risk | Reports included results both primary and secondary outcomes. |
| Recruitment bias | Low risk | Treatment allocation was revealed to the facilitating teams by the principal investigator, when baseline was completed. |
| Baseline imbalance | High risk | ”There were statistically significant differences between the intervention group and control |
| Loss of cluster | Low risk | Not loss cluster |
| Incorrect analysis | Low risk | “The effect of clustering was taken into account and adjusted for when if the ICC had a value greater than 5%. Logistical regressions were performed to detect differences between groups and adjust for possible confounders” |