| Literature DB >> 29546613 |
Tim Michael Feenstra1, Chris Dickhoff2, Jaap Deunk3.
Abstract
PURPOSE: Tube thoracostomy is frequently used in thoracic trauma patients. However, there is no consensus on whether low pressure suction or water seal is the optimal method of tube management. Against this background, we performed a systematic review of studies comparing suction and water seal management of chest tubes placed for traumatic chest injuries in adults. Evaluated outcomes are duration of chest tube treatment, length of stay in hospital, incidence of persistent air leak, clotted hemothorax, and the need for (re-)interventions.Entities:
Keywords: Chest tube; Suction; Trauma; Tube thoracostomy; Water seal
Mesh:
Year: 2018 PMID: 29546613 PMCID: PMC6267148 DOI: 10.1007/s00068-018-0942-7
Source DB: PubMed Journal: Eur J Trauma Emerg Surg ISSN: 1863-9933 Impact factor: 3.693
Fig. 1PRISMA flow chart of literature search and article selection
Characteristics of included studies
| First author | Year | Total patients | Suction | Water seal | Injurya | Indication for tube thoracostomyb | ||
|---|---|---|---|---|---|---|---|---|
| Male (%) | Female (%) | Male (%) | Female (%) | |||||
| Majumdar [ | 2014 | 60 | 23 (76.7%) | 7 (23.3%) | 25 (83.3%) | 5 (16.7%) | B, P | HT, HPT |
| Morales [ | 2014 | 110 | 54 (96.4%) | 2 (3.6%) | 51 (94.4%) | 3 (5.6%) | B, P | PT, HT, HPT |
| Muslim [ | 2008 | 100 | 38 (76%) | 12 (24%) | 36 (72%) | 14 (18%) | P | Not distinguished |
| Subtotal | 115 (84.6%) | 21 (15.4%) | 112 (83.6%) | 22 (16.1%) | ||||
| Total | 270 | 136 (50.4%) | 134 (49.6%) | |||||
aB blunt trauma, P penetrating trauma
bPT pneumothorax, HT hemothorax, HPT hemopneumothorax
Cochrane Collaboration’s tool for assessing risk of bias
| First author | Selection bias | Performance bias | Detection bias | Attrition bias | Reporting bias | Other bias | |
|---|---|---|---|---|---|---|---|
| Random sequence generation | Allocation concealment | Blinding of participants and personnell | Blinding of outcome assessment | Incomplete outcome data | Selective reporting | ||
| Majumdar [ | + | − | − | − | + | + | − |
| Morales [ | + | + | − | − | + | + | + |
| Muslim [ | + | ? | − | − | + | + | ? |
+ low risk of bias, − high risk of bias, ? unknown risk of bias
Fig. 2Meta-analysis of duration of chest tube treatment. A Mantel–Haenszel random effects model was used. Mean differences are shown with 95% confidence intervals
Fig. 3Meta-analysis of duration of length of stay in hospital. A Mantel–Haenszel random effects model was used. Mean differences are shown with 95% confidence interval
Fig. 4Meta-analysis of incidence of persistent air leak. A Mantel–Haenszel random effects model was used. Odds ratios are shown with 95% confidence intervals
Fig. 5Meta-analysis of incidence of persistent clotted hemothorax. A Mantel–Haenszel random effects model was used. Odds ratios are shown with 95% confidence intervals
Fig. 6Meta-analysis of incidence of (re-)interventions. A Mantel–Haenszel random effects model was used. Odds ratios are shown with 95% confidence interval
Summary of findings and GRADE quality of evidence score
| Outcomes | Anticipated absolute effectsa (95% CI) | Relative effect (95% CI) | No. of participants (studies) | Quality of evidence (GRADE) | |
|---|---|---|---|---|---|
| Risk with water seal | Risk with suction | ||||
| Duration of chest tube treatment | The mean duration of the chest tube treatment was 9.95 days | The mean duration of the chest tube treatment in the suction group was 3.38 days shorter (5.72–1.04 shorter) | – | 270 (3 RCT’s) | Very low |
| Length of stay in hospital (LOS) | The mean length of stay in hospital was 10.99 days | The mean length of stay in hospital in the suction group was 3.9 days shorter (6.01–1.8 shorter) | – | 270 (3 RCT’s) | Very low |
| Persistent air leak | 157 per 1.000 | 31 per 1.000 (11–85) | OR 0.17 (0.06–0.50) | 270 (3 RCT’s) | Moderate |
| Clotted hemothorax | 157 per 1.000 | 72 per 1.000 (25–195) | OR 0.42 (0.14–1.30) | 270 (3 RCT’s) | Low |
| (Re-)interventions | 155 per 1.000 | 68 per 1.000 (9–373) | OR 0.40 (0.05–3.25) | 170 (2 RCT’s) | Very low |
CI confidence interval, MD mean difference, OR odds ratio
aThe risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI)