| Literature DB >> 35782396 |
Kevin Chorath1, Sara Hobday1, Neeraj V Suresh1, Beatrice Go1, Alvaro Moreira2, Karthik Rajasekaran1,3.
Abstract
Objective: Enhanced recovery after surgery (ERAS) protocols are patient-centered, evidence-based pathways designed to reduce complications, promote recovery, and improve outcomes following surgery. These protocols have been successfully applied for the management of head and neck cancer, but relatively few studies have investigated the applicability of these pathways for other outpatient procedures in otolaryngology. Our goal was to perform a systematic review of available evidence reporting the utility of ERAS protocols for the management of patients undergoing outpatient otolaryngology operations.Entities:
Keywords: PSQI; enhanced recovery after surgery; otolaryngology; outpatient surgery; patient safety
Year: 2022 PMID: 35782396 PMCID: PMC9242417 DOI: 10.1002/wjo2.58
Source DB: PubMed Journal: World J Otorhinolaryngol Head Neck Surg ISSN: 2095-8811
Figure 1Preferred Reporting Items for Systematic Reviews and Meta‐Analyses flowchart of the systematic search strategy
Characteristics of studies describing enhanced recovery after surgery protocols for outpatient operations in otolaryngology
| Author (year) | Journal | Study type and date | Population | Mean age | Procedure | Limitations |
|---|---|---|---|---|---|---|
| Lawson et al. (1997) |
|
Prospective cohort June 1995–September 1995 | 100 Patients | – | Tonsillectomy and adenoidectomy | Controls were conventionally managed patients before pathway implementation |
| Pestian et al. (1998) |
| Retrospective cohort | 80 Patients, 50% male | 6.3 ± 3.06 | Tonsillectomy and adenoidectomy |
Retrospective analysis Controls were conventionally managed patients before pathway implementation |
| Liao et al. (2018) |
|
Randomized control trial December 2017–February 2018 | 50 Patients, 56% male | 36.4 ± 12.1 | Septoplasty |
No blinding of assessors or subjects Single‐institution experience |
| Wu et al. (2019) |
|
Randomized control trial January 2018–April 2018 | 102 Patients, 75% male | 39.4 ± 10.0 | Functional endoscopic sinus surgery |
Overlapping authors Single‐institution experience Small sample size No blinding of assessors or subjects |
| Wu et al. (2019) |
|
Randomized control trial January 2018–May 2018 | 74 Patients, 74% male | 38.7 | Functional endoscopic sinus surgery |
Overlapping authors Single‐institution experience SNOT‐22 questionnaire scores only reflect a subjective assessment of patients Lack of objective metrics of inflammation No blinding of assessors or subjects |
| Gao et al. (2020) |
|
Prospective cohort May 2018–October 2018 | 55 Patients, 80% male | 42.4 | Functional endoscopic sinus surgery |
Small sample size Single‐institution experience Nonrandomized design |
| Tan et al. (2020) |
|
Randomized control trial April 2018–February 2019 | 84 Patients, 25% male | 36.2 ± 10.7 | Tympanoplasty and mastoidectomy |
Small sample size Single‐institution experience |
| Zhang et al. (2020) |
|
Retrospective cohort April 2016–March 2017 | 394 Patients, 53% males | 5.4 ± 2.5 | Tonsillectomy and adenoidectomy |
Single‐institution experience Controls were conventionally managed patients before pathway implementation |
Abbreviation: SNOT‐22, sinononasal outcome test.
Components of enhanced recovery after surgery protocols across studies
| Author (year) | Preop education | Preop analgesia | Preop nutrition | Standard anesthesia protocol | Temperature | Fluid management | Mobilization | Postop analgesia | Postop nutrition |
|---|---|---|---|---|---|---|---|---|---|
| Lawson (1997) | + | + | + | + | + | + | + | ||
| Pestian (1998) | + | + | + | + | + | ||||
| Liao (2018) | + | + | + | + | + | + | + | + | |
| Wu (2019) | + | + | + | + | + | + | + | + | + |
| Wu (2019) | + | + | + | + | + | + | + | + | + |
| Gao (2020) | + | + | + | + | + | + | + | ||
| Tan (2020) | + | + | + | + | + | + | + | + | + |
| Zhang (2020) | + | + | + | + | + | + | + | + |
Outcomes assessed across studies evaluating enhanced recovery after surgery (ERAS) protocols( ± s)
| Author (year) | Hospital length of stay | Pain levels | Anxiety levels | Readmission (%) | Hospital costs ($) | Complications (%) | Other findings |
|---|---|---|---|---|---|---|---|
| Lawson (1997) |
Hospital LOS ERAS: 3 h postop (mean) Control: 4–7 h postop (mean) | – | – | – | – | – | |
| Pestian (1998) |
Hospital LOS ERAS: 14.8 ± 6.9 h postop Control: 17.8 ± 5.4 h postop | – | – |
Readmission rate ERAS: 2.5 Control: 2.5 |
Patient costs ERAS: 520 ± 136 Control: 590 ± 80 | – | – |
| Liao (2018) |
Hospital LOS ERAS: 4.4 ± 0.5 days Control: 5.8 ± 0.8 days |
VAS (POD 1, 2, & 3) ERAS: 3.5 ± 1.3 2.4 ± 0.9 2.0 ± 0.8 Control: 6.5 ± 2.2 6.0 ± 2.0 3.9 ± 0.9 |
SAS (preop, POD 3, POD 7) ERAS: 35.4 ± 6.2 31.6 ± 5.4 29.2 ± 5.0 Control: 43.6 ± 8.6 38.1 ± 10.4 31.2 ± 9.3 | – |
Hospital costs ERAS: 1252.5 ± 21.0 Control: 1333.7 ± 38.1 | – |
EBL: ERAS: 6.2 ± 2.1 ml Control: 6.6 ± 2.3 ml VAS sleep (POD 1 & 2) ERAS: 3.1 ± 1.4 2.6 ± 1.3 Control: 6.7 ± 2.4 6.5 ± 2.3 VAS nasal obstruction (POD 1, 2, 3) ERAS: 5.1 ± 1.2 3.5 ± 1.2 2.8 ± 0.9 Control: 9.2 ± 0.7 9.0 ± 0.8 5.5 ± 1.7 |
| Wu (2019) |
Hospital LOS ERAS: 4.7 ± 0.76 days Control: 8.3 ± 0.76 days |
VAS (2, 24, 48 h postop) ERAS: 0.7 ± 0.8 0.7 ± 0.8 0.3 ± 0.8 Control: 1.7 ± 3.8 |
SAS (preop) ERAS: 29 ± 8.4 Control: 44 ± 3.8 | – |
Hospital costs ERAS: 2595 ± 278.3 Control: 3233.7 ± 259.5 |
Postoperative complications ERAS: 3.8 Control: 4.0 |
Postop MOS‐SS sleep quality ERAS: 44.7 ± 5.3 Control: 28.3 ± 9.9 Postop CRP level ERAS: 2.6 ± 1.9 Control: 6.5 ± 4.0 |
| Wu (2019) | – | – | – | – | – |
Postoperative complications ERAS: 11.1 Control: 7.9 |
SNOT‐22 (preop, POD 1, POD 3, POD 6) ERAS: 39.89 ± 4.86 51.77 ± 5.59 48.22 ± 6.22 39.39 ± 4.73 Control: 40.52 ± 3.61 62.02 ± 3.86 51.11 ± 5.14 40.13 ± 3.31 |
| Gao (2020) | – |
VAS (2, 6, 24, 48 h postop) ERAS: 4 ± 1.7 2.3 ± 0.8 2.0 ± 1.7 1.3 ± 0.8 Control: 3.7 ± 2.4 4.0 ± 1.7 3.7 ± 1.7 2.7 ± 0.8 |
SAS (at discharge) ERAS: 28.7 ± 5.1 Control: 33.7 ± 4.2 | – | – |
Postoperative complications ERAS: 27.2 Control: 0 | – |
| Tan (2020) |
Hospital LOS ERAS: 4.75 ± 1.0 days Control: 5.0 ± 1.5 days |
VAS (postop) ERAS: 107.9 ± 0.0 Control: 1.0 ± 1.5 |
SAS ERAS: 29.8 ± 2.7 Control: 36.0 ± 10.0 | – |
Hospital costs ERAS: 105.1 ± 12.9 Control: 107.9 ± 13.4 |
Postoperative complications ERAS: 0 Control: 0 | – |
| Zhang (2020) | – |
Pain scores (POD 1, POD 3, POD 7) ERAS: 3.3 ± 0.7 2.3 ± 0.7 1.3 ± 0.7 Control: 3.7 ± 07 2.7 ± 0.7 1.7 ± 0.7 |
m‐YPAS (Preop) ERAS: 37.66 ± 6.68 Control: 47.70 ± 7.51 | – | – |
Postoperative complications ERAS: 1.92 Control: 10.22 |
Dietary Intake Score (POD 1, 3, & 7) ERAS: 0.7 ± 0.7 1.7 ± 0.7 2.3 ± 0.7 Control: 0.3 ± 0.7 1.3 ± 0.7 1.3 ± 0.7 |
Abbreviations: CRP, C reactive protein; EBL, estimated blood loss; ICU, intensive care unit; LOS, length of stay; MOS‐SS, Medical Outcomes Study Sleep Scale; m‐YPAS, modified Yale Preoperative Anxiety Scale; POD, postoperative day; postop, postoperative; SAS, Self‐Rating Anxiety Scale; SNOT‐22, sinononasal outcome test; VAS, Visual Analog Scale.
Statistically significant difference between intervention and control group (P < 0.05).
Nausea/emesis, hemorrhage, tumble, aspiration.
Nausea/emesis, hemorrhage, aspiration, dizziness.
Nausea/emesis, postoperative bleeding.
Nausea/emesis, dizziness, hematoma formation.
Fever, hemorrhage, wound infection, pneumonia.
Figure 2Strategies for implementation of enhanced recovery after surgery (ERAS) protocols