| Literature DB >> 32913210 |
Hai-Ming Huang1, Rui-Xia Chen1, Lin-Mei Zhu2, Wen-Shuai Zhao1, Xi-Jiu Ye1, Jian-Wei Luo1, Fu-Ding Lu1, Lei Zhang3, Xue-Ying Yang1, Yuan Yuan1, Jun Cao4.
Abstract
The incidence and mortality of primary liver cancer are very high and resection of tumor is the most crucial treatment for it. We aimed to assess the efficacy and safety of combined use of transversus abdominis plane (TAP) block and laryngeal mask airway (LMA) during implementing Enhanced Recovery After Surgery (ERAS) programs for patients with primary liver cancer. This was a prospective, evaluator-blinded, randomized, controlled parallel-arm trial. A total of 96 patients were enrolled (48 in each group). Patients in the control group received general anesthesia with endotracheal intubation, while patients in the TAP + LMA group received general anesthesia with LMA and an ultrasound-guided subcostal TAP block. The primary end-point was postoperative time of readiness for discharge. The secondary end-points were postoperative pain intensity, time to first flatus, quality of recovery (QoR), complications and overall medical cost. Postoperative time of readiness for discharge in the TAP + LMA group [7 (5-11) days] was shorter than that of the control group [8 (5-13) days, P = 0.004]. The postoperative apioid requirement and time to first flatus was lower in the TAP + LMA group [(102.8 ± 12.4) µg, (32.7 ± 5.8) h, respectively] than the control group [(135.7 ± 20.1) µg, P = 0.000; (47.2 ± 7.6) h, P = 0.000; respectively]. The QoR scores were significantly higher in the TAP + LMA group than the control group. The total cost for treatment in the TAP + LMA group [(66,608.4 ± 6,268.4) CNY] was lower than that of the control group [(84,434.0 ± 9,436.2) CNY, P = 0.000]. There was no difference in complications between these two groups. The combined usage of a TAP block and LMA is a simple, safe anesthesia method during implementing ERAS programs for patients with primary liver cancer. It can alleviate surgical stress, accelerate recovery and reduce medical cost.Entities:
Mesh:
Year: 2020 PMID: 32913210 PMCID: PMC7483533 DOI: 10.1038/s41598-020-71477-x
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379
The ERAS program adopted in this trial.
| Preoperative assessment, education and psychological counseling by talk, text and caption |
| Preparation before admission: cessation of smoking and alcohol for 14 days, quick walk for 30 min daily, oral enteral nutritional powder if plasma albumin ≤ 30 g/L, infuse red blood cell if Hb < 70 g/L |
| No preoperative use of sedatives or anticholinergic drugs |
| No bowel preparation, fasting for 6 h, and oral 10% glucose 500 ml 2 h before surgery |
| No routine placement of gastric tube; if necessary, remove it as soon as possible |
| Antibiotic prophylaxis 30 min before surgery |
| Use heparin to prevent deep vein thrombosis for high risk patients and monitor coagulation |
| Continuously monitor body temperature and maintain its stability by warmed blanket, warmed infusion and preheated peritoneal irrigation |
| Infuse crystal liquid mainly and restrict the volume (CVP ≤ 10 mmHg); rapidly infuse 200–300 ml colloidal fluid if severe hypotension occurs during the implementation of controlled-low CVP |
| No routine placement of peritoneal drainage tube; if necessary, remove it within 48 h |
| Anesthesia method: ETI general anesthesia for the control group, LMA general anesthesia combined with a subcostal TAP block for the TAP + LMA group |
| Use of short-acting anesthetics (i.e. remifentanil, sufentanil, propofol and sevoflurane) |
| Monitor anesthetic depth and maintain its stability |
| Intravenous tropisetron 10 mg for preventing postoperative nausea and vomiting |
| Multimodal postoperative analgesia: a. a single-shot regional block (local wound infiltration for the control group and a subcostal TAP block for the TAP + LMA group); b. patient-controlled intravenous analgesia (PCIA) with sufentanil; c. intravenous parecoxib 40 mg twice daily for 3 days; d. oral analgesic |
| Assess pain intensity with numerical rating scale (NRS) and inject additional analgesic when NRS score ≥ 5 |
| Intravenouslydrip dexamethasone 5 mg daily for 3 days to alleviate inflammation |
| Treatment of postoperative nausea and vomiting |
| Remove drainage tube and urinary tube as soon as possible |
Early oral intake: a little water on the day of surgery; liquid diet on 1st postoperative day; semi-liquid diet on 2nd postoperative day; normal diet from 3rd postoperative day on |
| Early mobilization: exercise in bed on the day of surgery; walk in the ward at least twice on 1st postoperative day; walk at least 4 times on 2nd postoperative day; continuously walk from 3rd postoperative day on |
| Use low molecular weight heparin to prevent deep vein thrombosis |
Figure 1Flow diagram for this trial.
Figure 2Procedures of LMA ventilation and subcostal TAP block. (A) Double-tube LMA: ventral side; (B) Double-tube LMA: back side; (C) Placement of LMA; (D) LMA ventilation and esophageal drainage; (E) LMA positioning by fiberoptic bronchoscopy; (F) positions of ultrasound probe for TAP block; (G) Ultrasound image of TAP block: inner site; (H). Ultrasound image of TAP block: lateral site. AT airway tube, DT esophageal drainage tube, M mask, IL inflation line, ST stomach tube, G glottal, VC vocal cord, ①: parasternal line, ②: anterior axillary line, ③: xiphoid, ④: costal arch, white rectangle: ultrasound probe, IS inner site, LS lateral site, N needle, LA local anesthetic, RA rectus abdominis, TA transversus abdominis, EO obliquus externus abdominis, IO obliquus internus abdominis.
Baseline Characteristics of the Patients.
| Variable | Control group (n = 41) | TAP + LMA group (n = 42) | |
|---|---|---|---|
| Age (years) | 51.4 ± 6.6 | 52.3 ± 6.3 | 0.532 |
| Sex (male/female) | 32/9 | 34/8 | 0.791 |
| BMI (kg/m2) | 22.3 ± 1.3 | 22.2 ± 1.7 | 0.765 |
| ASA physical status (II/III) | 29/12 | 28/14 | 0.690 |
| Preoperative Child–Pugh classification of liver function (A/B) | 31/10 | 34/8 | 0.555 |
| Number of tumor (1/2) | 28/13 | 33/9 | 0.289 |
| Diameter of tumor (mm) | 63.0 ± 17.2 | 64.8 ± 17.4 | 0.648 |
| Left lateral lobe | 8 | 10 | 0.635 |
| Left inner lobe | 6 | 7 | 0.799 |
| Right anteriorlobe | 18 | 15 | 0.446 |
| Right posterior lobe | 9 | 11 | 0.652 |
| Clinical stage of tumor (I/II)a | 20/21 | 25/17 | 0.326 |
| HCC | 32 | 34 | 0.743 |
| ICC | 5 | 3 | 0.436 |
| HCC-ICC | 4 | 5 | 0.753 |
| Grade I | 6 | 8 | 0.591 |
| Grade II | 26 | 23 | 0.423 |
| Grade III | 6 | 9 | 0.421 |
| Grade IV | 3 | 2 | 0.625 |
aAccording to the guidelines for diagnosis and treatment of primary liver cancer issued by the National Health Commission of China in 2017.
Primary and secondary outcomes.
| Variable | Control group (n = 41) | TAP + LMA group (n = 42) | |
|---|---|---|---|
| Postoperative time of readiness for discharge (days) | 8 (5–13) | 7 (5–11) | 0.004 |
| Postoperative apioid (sufentanil) requirement within 48 h (µg) | 135.7 ± 20.1 | 102.8 ± 12.4 | 0.000 |
| 2 h after surgery | 4.2 ± 1.4 | 3.3 ± 1.1 | 0.001 |
| 6 h after surgery | 4.8 ± 1.4 | 3.8 ± 1.1 | 0.001 |
| 24 h after surgery | 3.8 ± 1.1 | 3.1 ± 1.2 | 0.007 |
| 48 h after surgery | 3.0 ± 1.1 | 2.3 ± 0.9 | 0.001 |
| First mobilization off the bed (h) | 43.8 ± 5.1 | 28.1 ± 5.5 | 0.000 |
| Time to first flatus (h) | 47.2 ± 7.6 | 32.7 ± 5.8 | 0.000 |
| 1 day before surgery | 194.5 ± 3.3 | 193.8 ± 3.1 | 0.323 |
| 1 day after surgery | 169.5 ± 6.1 | 179.0 ± 5.6 | 0.000 |
| 3 days after surgery | 176.0 ± 5.1 | 187.8 ± 5.1 | 0.000 |
| Day of discharge | 192.0 ± 5.0 | 193.6 ± 4.2 | 0.113 |
| Nausea | 6 | 4 | 0.475 |
| Vomiting | 3 | 1 | 0.294 |
| Total cost for treatment (CNY) | 84,434.0 ± 9,436.2 | 66,608.4 ± 6,268.4 | 0.000 |
Perioperative profiles of anesthesia and surgery.
| Variable | Control group (n = 41) | TAP + LMA group (n = 42) | |
|---|---|---|---|
| t0 | 0.9 ± 0.2 | 0.9 ± 0.3 | 0.829 |
| t1 | 0.9 ± 0.2 | 1.0 ± 0.2 | 0.180 |
| t2 | 2.1 ± 0.5 | 1.6 ± 0.4 | 0.000 |
| t3 | 1.5 ± 0.4 | 1.1 ± 0.2 | 0.000 |
| t0 | 5.1 ± 0.5 | 4.9 ± 0.6 | 0.068 |
| t1 | 5.5 ± 0.5 | 5.2 ± 0.2 | 0.039 |
| t2 | 8.4 ± 0.8 | 7.8 ± 0.7 | 0.001 |
| t3 | 7.4 ± 1.0 | 7.1 ± 0.8 | 0.080 |
| Sevoflurane (ml) | 54.6 ± 9.4 | 39.3 ± 6.5 | 0.000 |
| Remifentanil (µg) | 1625.4 ± 264.8 | 1,072.9 ± 190.4 | 0.000 |
| Cis-atracurium (mg) | 35.8 ± 4.5 | 21.5 ± 3.7 | 0.000 |
| Nitroglycerin (mg) | 2.8 ± 0.6 | 2.7 ± 0.7 | 0.467 |
| Dobutamine (mg) | 11.2 ± 2.8 | 9.6 ± 2.4 | 0.006 |
| Norepinephrine (µg) | 1,203.7 ± 191.1 | 864.5 ± 108.8 | 0.000 |
| Duration of anethesia (min) | 268.3 ± 33.5 | 255.9 ± 35.3 | 0.103 |
| Duration of operation (min) | 222.8 ± 32.2 | 209.3 ± 35.2 | 0.073 |
| Duration of hepatectomy (min) | 122.9 ± 18.2 | 114.4 ± 15.4 | 0.023 |
| Duration of hepatic blood flow occlusion (min) | 26.5 ± 5.2 | 21.5 ± 3.5 | 0.000 |
| Bleeding volume (ml) | 480.5 ± 90.7 | 395.2 ± 68.8 | 0.000 |
| Infusion volume (ml) | 1839.0 ± 374.8 | 1631.0 ± 215.8 | 0.003 |
| Urine volume (ml) | 414.6 ± 86.8 | 500.0 ± 96.9 | 0.000 |
| Time to removing ETT or LMA (min) | 32.8 ± 4.5 | 19.3 ± 3.9 | 0.000 |
| PACU stay (min) | 114.0 ± 14.2 | 95.6 ± 11.4 | 0.000 |
t0 = before anesthesia, t1 = at surgical exploration, t2 = at the conclusion of surgery, t3 = at departure from PACU.
Complications related to anesthesia and surgery.
| Complications | Control group (n = 41) | TAP + LMA group (n = 42) | |
|---|---|---|---|
| Intraoperative reflux/aspiration | 0 | 0 | 1.000 |
| Intraoperative airway obstruction | 0 | 0 | 1.000 |
| Postoperative sore throat | 6 | 2 | 0.128 |
| Postoperative hoarse voice | 1 | 0 | 0.309 |
| Systemic poisoning from local anesthetic | 0 | 0 | 1.000 |
| Abdominal hematoma | 0 | 0 | 1.000 |
| Abdominal nerve injury | 0 | 0 | 1.000 |
| Abdominal visceral injury | 0 | 0 | 1.000 |
| Intraperitoneal hemorrhage | 0 | 0 | 1.000 |
| Ileus | 0 | 0 | 1.000 |
| Lung infection | 0 | 0 | 1.000 |
| Poor wound healing | 1 | 0 | 0.309 |
| Bile leakage | 0 | 0 | 1.000 |
| Readmission within 30 days | 1 | 0 | 0.309 |