| Literature DB >> 31256029 |
Doug Cary1,2, Kathy Briffa1, Leanda McKenna1.
Abstract
OBJECTIVES: The objectives of this scoping review were to identify (1) study designs and participant populations, (2) types of specific methodology and (3) common results, conclusions and recommendations from the body of evidence regarding our research question; is there a relationship between sleep posture and spinal symptoms.Entities:
Keywords: education; pain; sleep position; sleep posture; spinal symptoms; stiffness
Mesh:
Year: 2019 PMID: 31256029 PMCID: PMC6609073 DOI: 10.1136/bmjopen-2018-027633
Source DB: PubMed Journal: BMJ Open ISSN: 2044-6055 Impact factor: 2.692
Figure 1PRISMA flow diagram. PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses.
Mapping of study design and population characteristics
| Author | Study design | Population type | Sample size (Gender) | Age M (SD) |
| Abanobi | Epidemiological: case controlled | Welders in Owerri, Nigeria | 100 (male=100) | 35 (9) |
| Cary | Epidemiological: cross-sectional | Population of convenience in Esperance, Western Australia | 15 (male=7) | 44 (17) |
| Desouzart | Controlled pilot | Elderly participants in physical activity programme at Polytechnic Institute of Leiria, Portugal | 20 (male=0) | 62 (4) |
| Gordon | Epidemiological: cross-sectional | Every third household in Port Lincoln in South Australia | 812 (male=261) | Female 61 (10) |
M = mean, SD = standard deviation
Mapping of sleep posture measurement and symptoms
| Author | Sleep environment | Standard three sleep postures | Number of sleep postures | Sleep posture outcome measurement | Anatomical area | Symptom type | Symptom(s) characteristics | Symptom outcome measurement |
| Abanobi | Domestic | Y | 3 | SR | Lumbar | Pain | Past and present history | Questionnaire—face-to-face interview |
| Cary | Domestic | Y | 4 | SR+video recording | Cervical, lumbar, both, other | Pain, stiffness | Frequency (month) | Questionnaire written |
| Desouzart | Domestic | Y | 3 | SR | All spine | Pain | Intensity | Questionnaire written—pain VAS |
| Gordon | Domestic | Y | 5 | SR | Cervical | Pain, stiffness, HA, shoulder blade/arm pain | Frequency (week), duration | Questionnaire—structured telephone interview |
HA = headache; SR = self-report; VAS = Visual Analogue Scale; Y = yes.
Mapping of results, conclusions and recommendations
| Author | Results | Conclusions | Recommendations |
| Abanobi | ORs for LBP were in relation to a combined group of prone and side lying sleeping. ‘Sleeping with back (face up) increases the risk of developing LBP by 1.9 times.’ (p. 355) (95% CI 0.43 to 8.56) | ‘The result showed the possibility of reducing the burden of LBP by appropriate training and improvement in habits such as…bad sleeping postures.’ (p. 336) | Not provided |
| Cary | ‘The time spent in each of the sleeping postures… expressed as a percentage of the time spent asleep, did not differ significantly according to the level of morning symptoms’ (p. 5). Independent Samples Jonckheere-Terpstra Test; supine rj=0.03; | ‘Participants who spent greater periods of time in SSL, had less mornings of symptoms per month than those that slept in ¾ SL or prone.’ (p. 5) | Not provided |
| Desouzart | No between-group comparison reported. Between group effect size calculated to be 0.81 (95% CI −0.11 to 1.72). | ‘It may be concluded that the indication of the ideal way to lie down, which corresponds to a recommended sleeping posture with the ideal position to place the pillows, as well as the ideal way to get up.’ (p. 239) | Ideal sleep posture, pillow use and way to get up, as per experimental group, ‘is an added value for the prevention and decrease of the pain and/or discomfort in the spine in active seniors.’ (p. 239) |
| Gordon | ‘Subjects who reported sleeping mostly in an upright position were significantly more likely to report all waking symptoms of interest compared with subjects who slept in other positions.’ (p. 6) Waking cervical pain OR 2.5 (95% CI 1.1 to 5.5), cervical stiffness OR 2.6 (95% CI 1.1 to 5.8), headache OR 2.2 (95% CI 1.0 to 5.0), scapular/arm pain OR 2.5 (95% CI 1.1 to 5.3). | ‘On the basis of this research, SL can be confidently recommended as the best sleep position in terms of minimising waking symptoms.’ (p. 6) | |
*The CI was recalculated as it was suspected wrong due a typographical error. The original value was 0.431.
¾ SL = ¾ side lying; rj = effect size r for Jonckheere-Terpstra test.
LBP = low back pain; SSL = supported side lying; VAS = Visual Analogue Scale.
Critical appraisal of included studies using the Downs and Black checklist
| Section | Questions | Abanobi | Cary | Desouzart | Gordon | |
| Reporting | 1 | Is the hypothesis/aim/objective of the study clearly described? | Y | Y | Y | Y |
| 2 | Are the main outcomes to be measured clearly described in the Introduction or Methods section? | N | Y | Y | Y | |
| 3 | Are the characteristics of the patients included in the study clearly described? | Y | N | Y | X | |
| 4 | Are the interventions of interest clearly described? | X | X | Y | X | |
| 5 | Are the distributions of principal confounders in each group of subjects to be compared clearly described? | *Y | X | *Y | *Y | |
| 6 | Are the main findings of the study clearly described? | Y | Y | Y | Y | |
| 7 | Does the study provide estimates of the random variability in the data for the main outcomes? | Y | Y | Y | Y | |
| 8 | Have all important adverse events that may be a consequence of the intervention been reported? | X | X | N | X | |
| 9 | Have the characteristics of patients lost to follow-up been described? | X | X | Y | X | |
| 10 | Have actual probability values been reported (eg, 0.035 rather than<0.05) for the main outcomes except where the probability value is less than 0.001? | Y | Y | Y | N | |
| External validity | 11 | Were the subjects asked to participate in the study representative of the entire population from which they were recruited? | Y | Y | N | Y |
| 12 | Were those subjects who were prepared to participate representative of the entire population from which they were recruited? | U | N | N | N | |
| 13 | Were the staff, places and facilities where the patients were treated, representative of the treatment the majority of patients receive? | X | X | Y | X | |
| Internal validity: bias | 14 | Was an attempt made to blind study subjects to the intervention they have received? | X | X | U | X |
| 15 | Was an attempt made to blind those measuring the main outcomes of the intervention? | X | X | N | X | |
| 16 | If any of the results of the study were based on ‘data dredging’, was this made clear? | Y | Y | Y | Y | |
| 17 | In trials and cohort studies, do the analyses adjust for different lengths of follow-up of patients, or in case–control studies, is the time period between the intervention and outcome the same for cases and controls? | Y | X | Y | X | |
| 18 | Were the statistical tests used to assess the main outcomes appropriate? | Y | Y | Y | Y | |
| 19 | Was compliance with the intervention/s reliable? | X | X | U | X | |
| 20 | Were the main outcome measures used accurate (valid and reliable)? | Y | Y | Y | Y | |
| Internal validity: confounding | 21 | Were the patients in different intervention groups (trials and cohort studies) or were the cases and controls (case–control studies) recruited from the same population? | Y | X | Y | Y |
| 22 | Were study subjects in different intervention groups (trials and cohort studies) or were the cases and controls (case–control studies) recruited over the same period of time? | Y | X | Y | X | |
| 23 | Were study subjects randomised to intervention groups? | X | X | Y | X | |
| 24 | Was the randomised intervention assignment concealed from both patients and healthcare staff until recruitment was complete and irrevocable? | X | X | U | X | |
| 25 | Was there adequate adjustment for confounding in the analyses from which the main findings were drawn? | N | N | N | Y | |
| 26 | Were losses of patients to follow-up taken into account? | X | X | Y | X | |
| Power | 27 | Did the study have sufficient power to detect a clinically important effect where the probability value for a difference being due to chance is less than 5%? | N | X | N | N |
| Score | 14/17 | 9/12 | 19/28 | 12/14 | ||
| Percentage | 82 | 75 | 68 | 86 | ||
N = no = 0 points, Y = yes = 1 points, *Y = 2 points, U = unable to determine = 0, X = not applicable (see Quality of Evidence section).
Evidence levels = strong (>75%), moderate (50%–74%), limited (25%–49%) and poor quality (<24%).47