| Literature DB >> 35953683 |
Giuseppe Marinari1, Mirto Foletto2, Carlo Nagliati3, Giuseppe Navarra4, Vincenzo Borrelli5, Vincenzo Bruni6, Giovanni Fantola7, Roberto Moroni8, Luigi Tritapepe9, Roberta Monzani10, Daniela Sanna11, Michele Carron12, Rita Cataldo13.
Abstract
BACKGROUND: Enhanced recovery after bariatric surgery (ERABS) is an approach developed to improve outcomes in obese surgical patients. Unfortunately, it is not evenly implemented in Italy. The Italian Society for the Surgery of Obesity and Metabolic Diseases and the Italian Society of Anesthesia, Analgesia, Resuscitation and Intensive Care joined in drafting an official statement on ERABS.Entities:
Keywords: Anesthesia; Bariatric Surgery; Enhanced recovery after surgery; Obesity
Mesh:
Year: 2022 PMID: 35953683 PMCID: PMC9485178 DOI: 10.1007/s00464-022-09498-y
Source DB: PubMed Journal: Surg Endosc ISSN: 0930-2794 Impact factor: 3.453
Grading of level of evidence (from Oxford Centre for Evidence-Based Medicine 2011 Level of Evidence) [6]
| Question | Step 1 (Level 1*) | Step 2 (Level 2*) | Step 3 (Level 3*) | Step 4 (Level 4*) | Step 5 (Level 5*) |
|---|---|---|---|---|---|
| How common is the problem? | Local and current random sample surveys (or censuses) | Systematic review of surveys that allow matching to local circumstances** | Local non-random sample** | Case-series** | n/a |
| Is this diagnostic or monitoring test accurate? (Diagnosis) | Systematic review of cross sectional studies with consistently applied reference standard and blinding | Individual cross sectional studies with consistently applied reference standard and blinding | Non-consecutive studies, or studies without consistently applied reference standards** | Case–control studies, or “poor or non-independent reference standard** | Mechanism-based reasoning |
| What will happen if we do not add a therapy? (Prognosis) | Systematic review of inception cohort studies | Inception cohort studies | Cohort study or control arm of randomized trial* | Case-series or casecontrol studies, or poor quality prognostic cohort study** | n/a |
| Does this intervention help? (Treatment Benefits) | Systematic review of randomized trials or n-of-1 trials | Randomized trial or observational study with dramatic effect | Non-randomized controlled cohort/follow-up study** | Case-series, case–control studies, or historically controlled studies** | Mechanism-based reasoning |
| What are the COMMON harms? (Treatment Harms) | Systematic review of randomized trials, systematic review of nested case–control studies, n of-1 trial with the patient you are raising the question about, or observational study with dramatic effect | Individual randomized trial or (exceptionally) observational study with dramatic effect | Non-randomized controlled cohort/follow-up study (post-marketing surveillance) provided there are sufficient numbers to rule out a common harm. (For long-term harms the duration of follow-up must be sufficient.)** | Case-series, case–control, or historically controlled studies** | Mechanism-based reasoning |
| What are the RARE harms? (Treatment Harms) | Systematic review of randomized trials or n-of-1 trial | Randomized trial or (exceptionally) observational study with dramatic effect | |||
| Is this (early detection) test worthwhile? (Screening) | Systematic review of randomized trials | Randomized trial | Non-randomized controlled cohort/follow-up study** | Case-series, case–control, or historically controlled studies** | Mechanism-based reasoning |
*Level may be graded down on the basis of study quality, imprecision, indirectness (study PICO does not match questions PICO), because of inconsistency between studies, or because the absolute effect size is very small; Level may be graded up if there is a large or very large effect size
**As always, a systematic review is generally better than an individual study
Grading of quality of evidence (from US Preventive Services Task Force) [7]
| Grade | Description |
|---|---|
| A | The available evidence usually includes consistent results from multitude of well-designed, well-conducted, studies in representative care populations. These studies assess the effects of the service on the desired health outcomes. Because of the precision of findings, this conclusion is, therefore, unlikely to be strongly affected by the results of future studies. These recommendations are often based on direct evidence from clinical trials of screening, treatment, or behavioral interventions. High-quality trials designed as “pragmatic” or “effectiveness” trials are often of greater value in understanding external validity |
| B | The available evidence is sufficient to determine the effects of the service on targeted health outcomes, but confidence in the estimate is constrained by factors such as the number, size, or quality of individual studies in the evidence pool; some heterogeneity of outcome findings or intervention models across the body of studies; mild-to-moderate limitations in the generalizability of findings to routine care practice. As more information becomes available, the magnitude or direction of the observed effect could change, and this change may be large enough to alter the conclusion |
| C | The available evidence is insufficient to assess effects on health outcomes. Evidence is insufficient because of the very limited number or size of studies Inconsistency of direction or magnitude of findings across the body of evidence; critical gaps in the chain of evidence; findings are not generalizable to routine care practice; a lack of information on prespecified health outcomes; lack of coherence across the linkages in the chain of evidence. More information may allow an estimation of effects on health outcomes |
Grading of the strength of recommendation (from U.S. Preventive Services Task Force) [7]
| Grade | Definition | Suggestion for practice |
|---|---|---|
| A | The USPSTF recommends the service. There is high certainty that the net benefit is substantial | Offer or provide this service |
| B | The USPSTF recommends the service. There is high certainty that the net benefit is moderate or there is moderate certainty that the net benefit is moderate to substantial | Offer or provide this service |
| C | The USPSTF recommends selectively offering or providing this service to individual patients based on professional judgment and patient preferences. These is at least moderate certainty that the net benefit is small | Offer or provide this service for selected patients depending on individual circumstances |
| D | The USPSTF recommends against the service. There is moderate or high certainty that the service has no net benefit or that the harms outweigh the benefits | Discourage the use of this service |
| I | The USPSTF concludes that the current evidence is insufficient to assess the balance of benefits and harms of the service. Evidence is lacking, of poor quality, or conflicting, and the balance of benefits and harms cannot be determined | Read the clinical considerations section of USPSTF Recommendation Statement. If the service is offered, patients should understand the uncertainty about the balance of benefits and harms |
Effectiveness, safety, and items of Enhanced Recovery after Bariatric Surgery (ERABS) compared to standard approach
| Evidence | Strength of | Expert task force statement | ||
|---|---|---|---|---|
| Level | Quality | Recommendation | ||
| Length of hospital stay | 1 | A | A | ERABS reduces the duration of hospital stays |
| Risk of complications | 1 | A | A | ERABS is a safe approach for obese patients |
| Cost of surgery | 2 | B | A | Adopting an ERABS protocol does not increase the cost of surgery |
| Information and counseling | 2 | B | A | The information provided to the patient should not be limited to what is required for informed consent for both surgery and anesthesia; it should be adequate to provide realistic expectations of the ERABS approach |
| Patient optimization | 1 | A | A | Pre-operative optimization through smoking cessation, weight loss, blood glucose control, and the use of non-invasive ventilation (when indicated) is recommended in ERABS |
| Fasting | 1 | A | A | Clear liquids and solid food are recommended up to 2 h and 6 h, respectively, prior to the induction of anesthesia in ERABS |
| PONV prophylaxis | 1 | A | A | Strategies aimed at minimizing the risk of post-operative nausea and vomiting after general anesthesia are recommended for better patient outcomes in ERABS |
| Venous thromboembolism prophylaxis | 2 | B | A | Multimodal venous thromboembolism prophylaxis, including early patient mobilization, is recommended in ERABS |
| Antibiotic prophylaxis | 2 | B | A | Pre-operative intravenous antibiotic prophylaxis is recommended in ERABS |
| Monitoring | 1 | A | A | Proper perioperative monitoring is recommended in ERABS |
| Standardized anesthesia protocol | 1 | A | A | A standardized anesthesia approach is recommended in order to optimize outcomes in ERABS |
| 1-Airways management | 1 | A | A | A careful airways assessment is recommended in ERABS |
| 2-Preoxygenation | 1 | A | A | An adequate preoxygenation performed in ramped position is recommended in ERABS |
| 3-Tracheal intubation | 1 | A | A | Proper airway management in order to minimize difficulties is recommended in ERABS |
| 4-General anesthesia | 1 | A | A | General anesthesia is the anesthesiologic approach of choice in ERABS |
| 5-Neuromuscular blockade | 1 | A | A | Proper neuromuscular blockade management is recommended in ERABS |
| 6-Analgesia opioid sparing | 1 | A | A | Opioid-sparing or opioid-free anesthesia is recommended in ERABS |
| 7-Multimodal analgesia | 1 | A | A | Multimodal analgesia is recommended in ERABS to optimize pain control after surgery and to reduce or eliminate the use of opioids in the post-operative period |
| 8-Locoregional anesthesia | 1 | A | A | Locoregional anesthesia supports and complements general anesthesia in ERABS |
| 9-Protective lung ventilation | 1 | A | A | Protective mechanical lung ventilation during general anesthesia is recommended in ERABS |
| 10-Goal-directed fluid therapy | 3 | B | A | Proper perioperative fluid management is recommended. Goal-directed fluid therapy should be considered in ERABS |
| 11-Protected extubation | 1 | A | A | Extubation should be performed on an awake patient in the ramped position in ERABS |
| Nasogastric tube | 1 | A | A | Routine placement of the SNG does not improve outcomes in ERABS |
| Abdominal drainage | 2 | B | A | Routine use of abdominal drainage should be discontinued in ERABS |
| Bladder catheter | 4 | C | A | Routine use of bladder catheters should be abandoned in ERABS |
| Early mobilization | 3 | B | A | Early post-operative mobilization is recommended in ERABS |
| Early re-feeding | 1 | A | A | Early post-operative resumption of oral feeding is recommended in ERABS |
| Early discharge | 1 | A | A | Early discharge of the patient is recommended in ERABS. Adoption and verification of a discharge checklist upon discharge are recommended in ERABS |