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Post-tonsillectomy Pain Control in Adults

Primary Purpose

Pain, Postoperative, Postoperative Nausea and Vomiting, Postoperative Hemorrhage

Status
Terminated
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Norco (Hydrocodone and Acetaminophen)
Percocet (Oxycodone and Acetaminophen)
Dilaudid (hydromorphone)
Tylenol (Acetaminophen)
Sponsored by
University of Nebraska
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pain, Postoperative focused on measuring Tonsillectomy, Adenoidectomy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 18 years and older
  • Surgical indications: Chronic tonsillitis, Snoring, Sleep apnea
  • Surgical procedure: Tonsillectomy with monopolar cautery, hemostasis with monopolar cautery and/or suction cautery. The surgical procedure can also include Adenoidectomy with suction cautery

Exclusion Criteria:

  • Additional surgical procedures (i.e. UPPP (uvulopalatopharyngoplasty), septoplasty, inferior turbinate reduction) during same surgery
  • Pregnant females
  • Indications: Suspected malignancy
  • History of chronic pain or daily pain medication used for another medical problem
  • History of liver disease
  • Contraindications to preoperative Decadron
  • Contraindications to pain regimen medications (Tylenol, Norco, Percocet, Dilaudid)

Sites / Locations

  • University Nebraska Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

Tonsillectomy and Norco

Tonsillectomy and Percocet

Tonsillectomy and Dilaudid + Tylenol

Arm Description

This represents patients who will be randomized (1:3 chance) to postoperative pain control with Norco (Hydrocodone and Acetaminophen)

This represents patients who will be randomized (1:3 chance) to postoperative pain control with Percocet (Oxycodone and Acetaminophen)

This represents patients who will be randomized (1:3 chance) to postoperative pain control with Dilaudid (hydromorphone) and Tylenol (Acetaminophen)

Outcomes

Primary Outcome Measures

Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10
Daily pain level
Daily pain level on scale from 0-10

Secondary Outcome Measures

Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily oral liquid intake
Daily estimation of cups of liquids consumed
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Daily nausea/vomiting
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Weight Change from Baseline
Weight change comparing preoperative weight (kg) to postoperative weight (kg) at 2-3 weeks after surgery
Visit to emergency department after surgery
Yes/No answer for if patient needed to visit the emergency department after surgery for any reason related to their surgery
Post tonsillectomy hemorrhage
If patient had a post tonsillectomy hemorrhage and if any treatment was needed

Full Information

First Posted
January 14, 2015
Last Updated
July 11, 2023
Sponsor
University of Nebraska
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1. Study Identification

Unique Protocol Identification Number
NCT02358850
Brief Title
Post-tonsillectomy Pain Control in Adults
Official Title
Post-tonsillectomy Pain Control in Adults: a Randomized Prospective Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Terminated
Why Stopped
low enrollment
Study Start Date
January 2016 (Actual)
Primary Completion Date
January 24, 2019 (Actual)
Study Completion Date
January 24, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Nebraska

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a randomized prospective study to determine the optimal postoperative pain medication regimen for adults (18 years old and older) undergoing tonsillectomy with or without adenoidectomy for chronic tonsillitis and/or snoring and/or obstructive sleep apnea. All participants will undergo the same tonsillectomy surgical technique (with or without adenoidectomy) under general anesthesia and be randomized to one of three postoperative pain control regimens (all of which are commonly used pain medications for post-tonsillectomy pain): Norco (Hydrocodone and Acetaminophen) Percocet (Oxycodone and Acetaminophen) Dilaudid and Tylenol (Acetaminophen) Participants will be discharged home the day of surgery and will be sent home with questionnaires to assess their daily pain level, oral intake, amount of nausea/vomiting, and amount of pain medications taken for the 14 days following their surgery. Data will be collected and analyzed to determine if there is a difference in pain levels or oral intake or nausea/vomiting in the different pain regimen groups. Secondary endpoints will include weight change from preoperative weight to weight at 2-3 weeks after surgery in addition to postoperative complications including visits to the Emergency Department and post-tonsillectomy bleed rates. Participants will be seen 1-2 weeks following their surgery in the ENT (Ear, Nose and Throat) clinic per normal postoperative protocol and will not require any specific clinic visits related to this study.
Detailed Description
Hypotheses There is an optimal pain control regimen for post-tonsillectomy pain control in adults Post-tonsillectomy pain levels in adults peak around postoperative day number seven Post-tonsillectomy adults return very slowly to normal (pre-surgery) oral intake and diet Purpose To assess daily post-tonsillectomy pain level in adults for the two weeks after surgery To determine if there is an optimal post-tonsillectomy pain control regimen in adults for the two weeks after surgery To determine oral intake levels in post-tonsillectomy adults for the two weeks after surgery To determine daily amounts of nausea/vomiting in post-tonsillectomy adults for the two weeks after surgery To determine the change in weight in the two to three weeks after surgery Study Background Tonsillectomy (with or without adenoidectomy) is a very common procedure in children and adults. The most common indications for tonsillectomies include chronic tonsillitis and/or obstructive sleep apnea. While many studies have examined the optimal postoperative pain control regimen in children, the optimal pain control regimen in adults remains poorly studied and understood. Literature regarding post-tonsillectomy pain in adults has primarily focused on the specific tonsillectomy surgical technique (there are many) rather than the exact medications used for pain control. Interestingly, some of these aforementioned studies did not include the name, type or quantity of pain medications given to their patients when the primary study endpoint was pain. Additional studies have examined the role of steroids, antibiotics, and/or pain medications given by Anesthesia while a patient is anesthetized and undergoing tonsillectomy to determine if this can reduce postoperative pain. IV steroids given perioperatively to adults undergoing tonsillectomy have less pain, nausea, and vomiting in the first few days after tonsillectomy. IV steroids are now routinely given before tonsillectomy by most practicing Otolaryngologists, including our senior authors. There are a limited number of studies looking at actual postoperative pain control regimens in adults. Most of these studies are limited in that they only looked at the first 24 hours following surgery rather than trending pain levels for the first week or two after surgery. Additional studies are limited because they are observational or prospective without comparative pain regimen groups (i.e. they gave all patients the same medications asked them their daily pain levels). Furthermore, a majority of studies involving postoperative pain control used a "cold steel" technique tonsillectomy, which is uncommonly practiced in the United States by Otolaryngologists, who prefer the use of electrocautery devices for tonsillectomy. It is well known and accepted that cautery causes more postoperative pain due to thermal tissue injury, however it allows for a straightforward surgery with better intraoperative control of bleeding. Furthermore, randomized prospective studies for postoperative pain control following cautery tonsillectomy are lacking in the literature. It is well known that the expected recovery period for adults is 2-4 weeks, during which they cannot work or do any strenuous activity. We would argue that the first 24 hours after tonsillectomy is actually better tolerated by adults because they have received high potency narcotics (usually through their IV) during and right after surgery. Therefore a more meaningful time period to study would be postoperative day number 1 - 14, when the patient is at home and the pain is most severe (most patients state that their pain peaks around postoperative number 5-7). Pain control is incredibly important issue in the post-tonsillectomy patient. If they have too much pain, they will not drink or eat enough to stay hydrated and nourished. This can lead to electrolyte abnormalities and dehydration requiring visits to the Emergency Department with or without admission to the hospital. The purpose of this study is to evaluate post-tonsillectomy pain control in adults using three randomized medication regimens. All patients would undergo the same surgical technique to avoid confounding variables. Surgeries would be performed by Otolaryngology - Head and Neck Surgery Residents under the direct supervision of Otolaryngology staff attending surgeons. All of the proposed pain regimens are commonly accepted regimens used by practicing Otolaryngologists for adults. Patients would be asked to complete a questionnaire that numerically evaluates their daily: pain level, amount of oral intake, amount of nausea/vomiting, and amount of pain medications used. They would asked to mail in their results or return the clinic. Additional information would be collected from the patients and/or their medical records including visits to the emergency department, readmissions to the hospital, and postoperative complications including post-tonsillectomy bleeding. Data would be compiled and analyzed to determine the typical postoperative pain levels, daily oral intake level, and to compare the different pain regimens to determine if one is superior. It is important to note that there are accepted risks of general anesthesia and undergoing tonsillectomy with or without adenoidectomy. Participation in this study would not change any of the accepted risk of undergoing the surgical procedure. The risks commonly discussed with patients before tonsillectomy with or without adenoidectomy include failure to resolve chronic throat infections, failure to resolve obstructive sleep apnea, voice changes after surgery, damage to lips/teeth/tongue, taste changes, dehydration, need to return to the emergency department, need for admission to the hospital, and 3-5% risk of post-tonsillectomy bleeding that may result in need for additional surgical procedures and/or blood transfusions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pain, Postoperative, Postoperative Nausea and Vomiting, Postoperative Hemorrhage, Body Weight Changes
Keywords
Tonsillectomy, Adenoidectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
27 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tonsillectomy and Norco
Arm Type
Active Comparator
Arm Description
This represents patients who will be randomized (1:3 chance) to postoperative pain control with Norco (Hydrocodone and Acetaminophen)
Arm Title
Tonsillectomy and Percocet
Arm Type
Active Comparator
Arm Description
This represents patients who will be randomized (1:3 chance) to postoperative pain control with Percocet (Oxycodone and Acetaminophen)
Arm Title
Tonsillectomy and Dilaudid + Tylenol
Arm Type
Active Comparator
Arm Description
This represents patients who will be randomized (1:3 chance) to postoperative pain control with Dilaudid (hydromorphone) and Tylenol (Acetaminophen)
Intervention Type
Drug
Intervention Name(s)
Norco (Hydrocodone and Acetaminophen)
Other Intervention Name(s)
Norco
Intervention Description
Norco (Hydrocodone and Acetaminophen) 5/325 mg tab Take 1-2 tabs by mouth every 4-6 hours PRN (as needed) pain following Tonsillectomy for 14 days
Intervention Type
Drug
Intervention Name(s)
Percocet (Oxycodone and Acetaminophen)
Other Intervention Name(s)
Percocet
Intervention Description
Percocet (Oxycodone and Acetaminophen) 5/325 mg tab Take 1-2 tabs by mouth every 4-6 hours PRN pain following Tonsillectomy for 14 days
Intervention Type
Drug
Intervention Name(s)
Dilaudid (hydromorphone)
Other Intervention Name(s)
Dilaudid
Intervention Description
Dilaudid (hydromorphone) 2 mg tab Take 1-2 tabs by mouth every 4-6 hours PRN pain following Tonsillectomy for 14 days
Intervention Type
Drug
Intervention Name(s)
Tylenol (Acetaminophen)
Other Intervention Name(s)
Tylenol
Intervention Description
Tylenol (Acetaminophen) 325 mg tab Take 1-2 tabs by mouth every 4-6 hours PRN pain following Tonsillectomy for 14 days
Primary Outcome Measure Information:
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 1
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 2
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 3
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 4
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 5
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 6
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 7
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 8
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 9
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 10
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 11
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 12
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 13
Title
Daily pain level
Description
Daily pain level on scale from 0-10
Time Frame
Postoperative day 14
Secondary Outcome Measure Information:
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 1
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 2
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 3
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 4
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 5
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 6
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 7
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 8
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 9
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 10
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 11
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 12
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 13
Title
Daily oral liquid intake
Description
Daily estimation of cups of liquids consumed
Time Frame
Postoperative day 14
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 1
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 2
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 3
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 4
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 5
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 6
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 7
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 8
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 9
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 10
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 11
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 12
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 13
Title
Daily nausea/vomiting
Description
Daily amount of nausea/vomiting with a scale from 0 - 4. 0 = no nausea = mild nausea = significant nausea and/or dry heaving = vomiting
Time Frame
Postoperative day 14
Title
Weight Change from Baseline
Description
Weight change comparing preoperative weight (kg) to postoperative weight (kg) at 2-3 weeks after surgery
Time Frame
Preoperative weight compared to postoperative weight at 2-3 weeks after surgery
Title
Visit to emergency department after surgery
Description
Yes/No answer for if patient needed to visit the emergency department after surgery for any reason related to their surgery
Time Frame
Within 14 days after surgery
Title
Post tonsillectomy hemorrhage
Description
If patient had a post tonsillectomy hemorrhage and if any treatment was needed
Time Frame
Within 14 days after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18 years and older Surgical indications: Chronic tonsillitis, Snoring, Sleep apnea Surgical procedure: Tonsillectomy with monopolar cautery, hemostasis with monopolar cautery and/or suction cautery. The surgical procedure can also include Adenoidectomy with suction cautery Exclusion Criteria: Additional surgical procedures (i.e. UPPP (uvulopalatopharyngoplasty), septoplasty, inferior turbinate reduction) during same surgery Pregnant females Indications: Suspected malignancy History of chronic pain or daily pain medication used for another medical problem History of liver disease Contraindications to preoperative Decadron Contraindications to pain regimen medications (Tylenol, Norco, Percocet, Dilaudid)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Samuel Pate, M.D.
Organizational Affiliation
University of Nebraska Medical Center Department of Otolaryngology - Head and Neck Surgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Nebraska Medical Center
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68198
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18656720
Citation
Lee SW, Jeon SS, Lee JD, Lee JY, Kim SC, Koh YW. A comparison of postoperative pain and complications in tonsillectomy using BiClamp forceps and electrocautery tonsillectomy. Otolaryngol Head Neck Surg. 2008 Aug;139(2):228-34. doi: 10.1016/j.otohns.2008.04.004.
Results Reference
background
PubMed Identifier
16399189
Citation
Parsons SP, Cordes SR, Comer B. Comparison of posttonsillectomy pain using the ultrasonic scalpel, coblator, and electrocautery. Otolaryngol Head Neck Surg. 2006 Jan;134(1):106-13. doi: 10.1016/j.otohns.2005.09.027.
Results Reference
background
PubMed Identifier
16885729
Citation
Noordzij JP, Affleck BD. Coblation versus unipolar electrocautery tonsillectomy: a prospective, randomized, single-blind study in adult patients. Laryngoscope. 2006 Aug;116(8):1303-9. doi: 10.1097/01.mlg.0000225944.00189.e9.
Results Reference
background
PubMed Identifier
21812940
Citation
Diakos EA, Gallos ID, El-Shunnar S, Clarke M, Kazi R, Mehanna H. Dexamethasone reduces pain, vomiting and overall complications following tonsillectomy in adults: a systematic review and meta-analysis of randomised controlled trials. Clin Otolaryngol. 2011 Dec;36(6):531-42. doi: 10.1111/j.1749-4486.2011.02373.x.
Results Reference
background
PubMed Identifier
11200596
Citation
Thorneman G, Akervall J. Pain treatment after tonsillectomy: advantages of analgesics regularly given compared with analgesics on demand. Acta Otolaryngol. 2000 Oct;120(8):986-9. doi: 10.1080/00016480050218744.
Results Reference
background
PubMed Identifier
16211736
Citation
Naesh O, Niles LA, Gilbert JG, Ammar MM, Phibbs PW, Phillips AM, Khrapov AV, Robert AJ, McClintock A. A randomized, placebo-controlled study of rofecoxib with paracetamol in early post-tonsillectomy pain in adults. Eur J Anaesthesiol. 2005 Oct;22(10):768-73. doi: 10.1017/s0265021505001274.
Results Reference
background
PubMed Identifier
15352967
Citation
Hiller A, Silvanto M, Savolainen S, Tarkkila P. Propacetamol and diclofenac alone and in combination for analgesia after elective tonsillectomy. Acta Anaesthesiol Scand. 2004 Oct;48(9):1185-9. doi: 10.1111/j.1399-6576.2004.00473.x.
Results Reference
background
PubMed Identifier
11802045
Citation
Salonen A, Kokki H, Nuutinen J. Recovery after tonsillectomy in adults: a three-week follow-up study. Laryngoscope. 2002 Jan;112(1):94-8. doi: 10.1097/00005537-200201000-00017.
Results Reference
background
PubMed Identifier
18033974
Citation
Ashbach MN, Ostrower ST, Parikh SR. Tonsillectomy techniques and pain: a review of randomized controlled trials and call for standardization. ORL J Otorhinolaryngol Relat Spec. 2007;69(6):364-70. doi: 10.1159/000108369. Epub 2007 Nov 23.
Results Reference
background

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Post-tonsillectomy Pain Control in Adults

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