Quadratus Lumborum Block, Thoracic Paravertebral Block, Postoperative Analgesia, Hepatectomy
Conditions
Brief summary
Pain after hepatectomy can interfere with the patients' recovery and may contribute to developing long term pain. Opioids, e.g. morphine, fentanyl, sufentanil, works well for postoperative analgesia, but have several side effects such as nausea, vomiting and itching which may be severe enough to affect patients' recovery. In some cases, opioids may cause constipation and urinary retention within the first 24 hours after surgery. Thus, several ultrasound-guided nerve block procedures have been applied to provide postoperative analgesia. Ultrasound-guided thoracic paravertebral block (TPVB) is one of the most used nerve block methods using for post-hepatectomy analgesia. However, in some cases, ultrasound-guided TPVB can cause pneumothorax, hemopneumothorax, and higher block level. The quadratus lumborum block (QLB) is a new developed nerve block which can provide a widespread analgesic effect from T7 to L1. Therefore, this study is to determine whether QLB or TPVB have a better pain control with fewer side effects and complications after laparoscopic and open hepatectomy. The adequate pain control will be assessed by their visual analogue score (VAS) and the postoperative quality of recovery scale (QoR-15, Chinese Version). Additionally, the side effect and complications profile of these two nerve block techniques will also be recorded and compared.
Interventions
PCIA solution: 2 μg/kg weight sufentanil and 8.96 mg tropisetron mesylate diluted in 100 ml normal saline；PCIA parameters: loading dose: 2 ml, background infusion: 2ml/h, bolus: 0.5ml, lockout-time: 15min; PCA duration: 48 hours from the end of suturing
OTHERQuadratus Lumborum Block
Ultrasound-guided Quadratus lumborum block: A broadband (5-8 MHz) convex transducer will be placed transversely in the abdominal flank above the iliac crest to identify the external oblique, internal oblique, transversus abdominis muscles and aponeurosis. Then the external oblique muscle will be followed posteriorly until its posterior border is visualized (hook sign), and the posterior aspect of the Quadratus lumborum muscle is confirmed. A 22-G, 11-mm, short-bevel facet needle will be advanced under direct ultrasound visualization in-plane from anterolateral to postero-medial. Then the 20 ml of 0.375 % ropivacaine will be injected into the lumbar inter-facial triangle (LIFT) behind the quadratus lumborum muscle using hydro-dissection.
OTHERThoracic Paravertebral Block
Ultrasound-guided Thoracic paravertebral block: The patient is placed in the lateral position, the spinous processes of T6 and T8 are identified and marks are made 2cm lateral to the spinous processes. The linear(L12-3) probe is placed transversally at the mark to identify the paravertebral space. Then a 22-G needle is inserted in-plane from lateral to medial and advanced until the tip reached the paravertebral space surrounded by the parietal pleura and the superior costotransverse ligament. Then 15 ml 0.375% ropivacaine is injected into the paravertebral space of T6 and T8.
Sponsors
Nanfang Hospital, Southern Medical University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Caregiver)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* Patients aged between 18 and 65 years old for selective hepatectomy from nanfang Hospital, Southern Medical University * American Society of Anesthesiologists (ASA) risk class I-III; * Body Mass Index (BMI) is not lesser than 18 and not greater than 30;
Exclusion criteria
* Patients refuse to participate * Allergy to the any agents used in current clinical trial; * Dependence, tolerance or excessive sensitivity to the anesthetics and psychotropic drugs; * Patients with nerve block contraindications (e.g. local infection of skin or soft tissue in injection site, serious bleeding tendency or hemorrhagic disease, anatomical aberration which make anesthesiologist cannot perform the ultrasound-guided nerve block, allergic history of local anesthetics, etc.); * Previous abdominal surgery (except for diagnostic biopsy); * New York Heart Association (NYHA) classification of cardiac function grade IV and/or Ejection Fraction (EF)≤55%; * Child-Pugh grading * Liver function of grade C (Child-Pugh grading) * Glomerular filtration rate≤60ml/min/1.73m2; * Obstructive sleep apnea syndrome; * Chronic obstructive pulmonary disease, asthma, active tuberculosis; * Cardiac rhythm disorders; * Past or present history of nervous system diseases and mental disorders (such as epilepsy, Alzheimer's disease, Parkinsonism syndrome, depression,etc.); * Autoimmune diseases (such as lupus erythematosus, rheumatoid arthritis,etc.) * Malignant tumors of other systems; * Other operations are required during the same period;
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| VAS | From 1 day before the surgery to the 2 days after surgery | The visual analogue scale (VAS) is a psychometric response scale which can be used in questionnaires. It is a measurement instrument for subjective characteristics or attitudes that cannot be directly measured. When responding to a VAS item, respondents specify their level of agreement to a statement by indicating a position along a continuous line between two end-points. In current study visual analogue scale is be adopt to assess pain of patients. The VAS ranges from 0-10,0 represents no pain and 10 represents the worst pain. |
| QoR-15/Quality of Recovery Scale 15(QoR-15) | From 1 day before the surgery to the 2 days after surgery | The Quality of Recovery-15 scale (QoR-15) is an easy-to-use score for assessing the quality of post-operative recovery. The QoR-15 is a 15-item questionnaire intended to measure QoR after anesthesia and surgery. It comprises five subscales: pain (n = 2), physical comfort (n = 5), physical independence (n = 2), psychological support (n = 2), and emotional state (n = 4) . Each item is scored from 0 to 10, and the possible total score ranges from 0 to 150. A higher total score means better patient QoR. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Opioids consumption during hepatectomy Intraoperative opioids consumption | At the end of surgical procedure | Total doses of opioids consumed during the surgical procedure intraoperatively |
| Opioids consumption after hepatectomy | Up to 48 postoperative hrs | Opioids consumption after hepatectomy which are administrated by Patient-controlled intravenous analgesia(PCIA) and by physician's order |
| First request of analgesia | Up to 48 postoperative hrs | Time to first request of rescue analgesic drug |
| Nausea | Up to 48 postoperative hrs | Incidence of postoperative nausea |
| Lower extremity muscle strength | Up to 48 postoperative hrs | The muscle strength is divided into 6 levels.To observe the flexion of quadriceps. |
| Respiratory depression | Up to 48 postoperative hrs | Incidence of postoperative respiratory depression |
| Pruritus | Up to 48 postoperative hrs | Incidence of postoperative pruritus |
| Sedation Score | Up to 48 postoperative hrs | A score to evaluate patients' sedation deepness Sedation score will be assessed with 'Modified Observer's assessment of alertness/sedation (OAA/S) score'. The OAA/S Scale is composed of the following categories: (1) responsiveness, (2) speech, (3) facial expression, and (4) eyes. The OAA/S Scale can be scored in two ways: the composite score, with a range of 1 (deep sleep) to 5 (alert), in any one of the four assessment categories and the sum of the four component scores, where responsiveness has possible scores of 1, 2, 3, 4 or 5, speech has scores of 2, 3, 4 or 5, and facial expression and eyes have scores of 3, 4 or 5. |
| Time to first off-bed activity | Up to discharge from hospital | Postoperative activity |
| Vomiting | Up to 48 postoperative hrs | Incidence of postoperative vomiting |
| Total opioids consumption | From admitting in operation room to 48 hours after hepatectomy | The total amount of opioids consumed during perioperative period |
Countries
China
Contacts
Primary ContactJunyun Fan, Bachelor
Backup ContactBingsha Chen, Bachelor
Outcome results
None listed