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Comparison of Different Approaches for Supraclavicular Block and Their Effects on Diaphragm Muscle Function

Primary Purpose

Phrenic Nerve Paralysis, Diaphragm Sellae Meningioma, Complications

Status
Completed
Phase
Phase 4
Locations
Turkey
Study Type
Interventional
Intervention
Bupivacaine HCl 0.5% Injectable Solution
Prilocaine HCl % 2 injectable solution
adrenaline amp 0.5mg
Ultrasound Guided Supraclavicular Block Corner pocket approach
Ultrasound Guided Supraclavicular Block Corner pocket + intracluster approach
Ultrasound Guided Supraclavicular Block multi approach
diagraphma muscle evaluation with ultrasound
Sponsored by
Bozyaka Training and Research Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Phrenic Nerve Paralysis focused on measuring Brachial Plexus Block, Phrenic Nerve Paralysis, Respiratory Complication, Complications, nerve block, Diaphragm

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients who are scheduled scheduled for hand, wrist, forearm, arm surgery
  • Patients who has informed consent for study
  • Patients with American Society of Anesthesiologists Physical Status Classification(ASA) I,II and III

Exclusion Criteria:

  • Patient's refusal to participate
  • Patients under 18 years of age
  • Patients with known local anesthetic allergy
  • Patients with Body mass index> 35
  • Patients diagnosed sepsis and bacteriemia,
  • Skin infection at the injection site,
  • History of coagulopathy or anticoagulant therapy
  • Patients with uncontrolled diabetes,
  • Uncoordinated patients,
  • Psychological and emotional lability,
  • Patients with anatomical disorders at application points
  • Pregnant patients

Sites / Locations

  • Izmir Bozyaka Training and Research Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

corner pocket

corner+intracluster

multi

Arm Description

The block will be performed by an experienced anesthesiologist in block applications under USG guidance. After the antisepsis of the area to be blocked, a 22G 50 mm stimulator needle will be used for the block . Intermittent negative aspiration will be performed during all procedures to detect possible vascular puncture. 20 ml of bupivacaine(Buvicaine HCl %0.5) and prilocaine(Priloc HCl %2) 1:1 mixture will be prepared in a way that there will be 5mcg adrenaline per ml.(9ml bupivacaine, 9ml prilocaine and 2ml saline with 50 mcg adrenaline per ml) Local anesthetic mixture will be given to the corner pocket - where the artery and the first rib intersect in the sonoanatomical image.

The block will be performed by an experienced anesthesiologist in block applications under USG guidance. After the antisepsis of the area to be blocked, a 22G 50 mm stimulator needle will be used for the block . Intermittent negative aspiration will be performed during all procedures to detect possible vascular puncture20 ml of bupivacaine(Buvicaine HCl %0.5) and prilocaine(Priloc HCl %2) 1:1 mixture will be prepared in a way that there will be 5mcg adrenaline per ml.(9ml bupivacaine, 9ml prilocaine and 2ml saline with 50 mcg adrenaline per ml) 10 ml of the local anesthetic mixture will be given to the described corner pack and the remaining 10 ml into the largest nerve cluster (Intracluster injection).

The block will be performed by an experienced anesthesiologist in block applications under USG guidance. After the antisepsis of the area to be blocked, a 22G 50 mm stimulator needle will be used for the block . Intermittent negative aspiration will be performed during all procedures to detect possible vascular puncture. 20 ml of bupivacaine(Buvicaine HCl %0.5) and prilocaine(Priloc HCl %2) 1:1 mixture will be prepared in a way that there will be 5mcg adrenaline per ml.(9ml bupivacaine, 9ml prilocaine and 2ml saline with 50 mcg adrenaline per ml) Local anesthetic mixture will be administered by multi injection method between the nerve groups seen in the sonoanatomical image.

Outcomes

Primary Outcome Measures

Comparison of Three Different Approach for Supraclavicular Blocks Effects on Diaphragm Thickening Fraction
Several diaphragm images will be taken, at least three at the point of maximum thickening in TLC and at least three at minimum thickness in RV. On each B-mode image, diaphragm thickness will be measured from the middle of the pleural line to the middle of the peritoneal line. Then DTI will be calculated as a percentage from the formula: (Max thickness at the end of inspiration - Max thickness at the end of the expiration) / Max thickness at the end of the expiration. All patients will be evaluated with USG in a head-up position facing the side to be operated 30 minutes after the block is performed.

Secondary Outcome Measures

The sensory block level
Sensory block level; The level of block that will occur in the sensory areas of axillary, median, radial, ulnar, musculocutaneous, cutaneous brachia and cutaneous antebraki medialis nerves will be evaluated by performing a pinprick test and its level will be recorded (0 = Painful, no block; 1 = Partial block-analgesia, only feeling of touch; 2 = Complete block, no pain).
The motor block level
It will be evaluated with the Modified Bromage scale: 0 = No blocks, he can lift his arm, 1= Motor power is low but the arm is movable, 2 = The arm is immobile but the fingers are movable, 3 = Complete block, no movement in hand or arm
Block success
It will be defined as the presence of the pinprick test in the musculacutaneous, radial, ulnar, median, cutaneous antebraki nerves with no pain or only feeling of touch. If any of these nerves are not blocked, it will be considered a failed block.
Postoperative analgesia time
Numeric rating scale; patient values pain between 0 and 10; 0 = No pain-10 = Intractable pain
Pain Score Follow-up
Numeric rating scale; patient values pain between 0 and 10; 0 = No pain-10 = Intractable pain
Block return time
Sensory (the time from local anesthetic injection until the patient fully perceives the upper limb) and motor (the time from local anesthetic injection to the moment the patient's upper limb regains muscle strength) will be recorded as the time to return the block.
Block application time
It will be defined as the time from the moment the needle passes through the skin until the local anesthetic is given and the needle is withdraw.
Block onset time
It will be defined as the time required to initiate anesthesia and analgesia in all 5 distal nerves from the local anesthetic injection.
Patient and surgeon satisfaction
Patient and surgeon satisfaction will be evaluated as: 1 = Complete dissatisfaction, 2 = Moderate satisfaction, 3 = Full satisfaction after the procedure.
Undesirable side effects:
Recorded when there is vascular puncture, hematoma, signs of LA toxicity, respiratory distress, pneumothorax, and Horner Syndrome.
The first opioid requirement hour
The first hour of opioid requirement of the patients will be recorded.(When NRS> 3) Opioids(Tramadol) will be administered to patients in case demanded.
24-hour total opioid consumption
It will be recorded how much opioid he needs to use for 24 hours.Opioids(Tramadol) will be administered to patients in case demanded.
Chronic pain questionnaire
After 6 months, patients will be called and questioned by phone.

Full Information

First Posted
February 8, 2021
Last Updated
June 11, 2023
Sponsor
Bozyaka Training and Research Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04756050
Brief Title
Comparison of Different Approaches for Supraclavicular Block and Their Effects on Diaphragm Muscle Function
Official Title
Comparison of Different Approaches for Supraclavicular Block and Their Effects on Diaphragm Muscle Function Evaluated With Diaphragm Thickening Fraction
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
February 16, 2021 (Actual)
Primary Completion Date
August 15, 2021 (Actual)
Study Completion Date
March 2, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bozyaka Training and Research Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Brachial plexus blocks used for anesthesia in upper extremity operations can be performed with interscalene, axillary, supraclavicular and infraclavicular approaches. Plexus blockage can be performed under the guidance of needle nerve stimulation, artery palpation or ultrasonography (USG). Nowadays, the simultaneous use of USG during the block allows the protection of structures such as nerves, pleura and vessels, and allows practitioners to see the needle and the spread of local anesthetic during the injection. Although supraclavicular block seems to be advantageous because the brachial plexus is more compact and superficial in this region, it has a disadvantage of being close to the pleura. (Increased risk of pneumothorax) With the use of USG, this risk has decreased and the supraclavicular block has become an alternative to infraclavicular block, which is widely used in upper extremity surgery. Due to the compact structure of the brachial plexus trunk at the first rib level, the application of the block is easier and the block formation is faster due to the peripheral spread of the local anesthetic. With the spread of local anesthetic to C3-C5 nerve roots in the brachial plexus, paralysis can be seen in the ipsilateral phrenic nerve up to 67%. Patients who will be operated on, especially in patients with respiratory distress, may experience respiratory distress due to the dysfunction of that side diaphragm muscle. With the help of ultrasound, the inspiratory and end-expiratory thickness of the diaphragm is measured with the Diaphragm Thickness Index (DTI), which is a new and effective method used as a mechanical ventilator weaning index in intensive care units. With this method, we can examine the effect of phrenic nerve block on diaphragm muscle due to local anesthesia in the acute period. DTI is calculated as a percentage from the following formula: (Max thickness at the end of inspiration - Max thickness at the end of the expiration) / Max thickness at the end of the expiration. By comparing 3 different approaches used in supraclavicular block, we aimed to investigate the most appropriate block approach in terms of effectiveness, speed, complication rate, effects on diaphragm and 6 months effects.
Detailed Description
In this prospective randomized double-blind study, patients will be divided into 3 groups using a computer program. Standard monitoring (ECG, pulse oximetry, noninvasive blood pressure) will be applied to the patients who will then be taken to the block application room . After the peripheral vascular access is established on the hand that will not be operated on, premedication will be provided with 2 mg iv midazolam. The blocks will be performed by an experienced anesthesiologist with the USG guidance. Block evaluation and measurements will be made by a different experienced anesthesiologist. After the antisepsis of the area to be blocked, a 22G 50 mm stimulator needle will be used for the block. Intermittent negative aspiration will be performed during all procedures to detect possible vascular puncture. The local anesthetic mixture we routinely use in our clinic will be used. 20 ml of bupivacaine(Buvicaine HCl %0.5) and prilocaine(Priloc HCl %2) 1:1 mixture will be prepared in a way that there will be 5mcg adrenaline per ml.(9ml bupivacaine, 9ml prilocaine and 2ml saline with 50 mcg adrenaline per ml) The ultrasound probe will be placed on the clavicle, the supraclavicular block will be applied in the coronal oblique plane using the in-plane technique. 3 different approaches of supraclavicular block will be compared. Approaches share the same probe position and needle entry point but differ in where the local anesthetic is given. Group 1: Local anesthetic mixture will be given to the corner pocket - where the artery and the first rib intersect in the sonoanatomical image. Group 2: 10 ml of the local anesthetic mixture will be given to the described corner pack and the remaining 10 ml into the largest nerve cluster (Intracluster injection). Group 3: Local anesthetic mixture will be administered by multi injection method between the nerve groups seen in the sonoanatomical image. The diaphragm thickening fraction and evaluations will be made by another experienced anesthesiologist, double-blindness will be achieved by being blind to the patient's group. Effects of phrenic nerve block on diaphraghma muscle will be evaluated by diaphraghma thickining fraction.All patients will be evaluated with USG in a head-up position facing the side to be operated before and 30 minutes after the block is performed.The probe will be placed perpendicular to the chest wall, in the eighth or ninth intercostal space, between the anterior axillary and midaxillary lines, 0.5 to 2 cm below the costophrenic sinus. The diaphragm will be viewed as a structure with three distinct layers, including two parallel echoic lines (Diaphragmatic pleura and peritoneum) and a hypoechoic line between them (Diaphragm muscle) . The patient will be instructed to breathe up to total lung capacity (TLC) and then exhale to residual volume (RV). Several diaphragm images will be taken, at least three at the point of maximum thickening in TLC and at least three at minimum thickness in RV. On each B-mode image, diaphragm thickness will be measured from the middle of the pleural line to the middle of the peritoneal line. Then DTI will be calculated as a percentage from the following formula: (Max thickness at the end of inspiration - Max thickness at the end of the expiration) / Max thickness at the end of the expiration. With this formula, we can determine the involvement of phrenic nerve by looking at the rate of diaphragm thickening before and after supraclavicular block in different groups. As a first line rescue anesthesia, patients will receive sedoanalgesia with remifentanil infusion. Laryngeal mask and general anesthesia will be commenced if needed. The postoperative analgesic regimen will routinely contain 1000 mg IV acetaminophen (3x1) and, if necessary, 1 mg opioid (Tramadol) per kg will be given.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Phrenic Nerve Paralysis, Diaphragm Sellae Meningioma, Complications, Respiratory Complication, Nerve Block, Brachial Plexus Block
Keywords
Brachial Plexus Block, Phrenic Nerve Paralysis, Respiratory Complication, Complications, nerve block, Diaphragm

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Three groups involved. 3 different approaches of supraclavicular block will be compared. Approaches share the same probe position and needle entry point but differ in where the local anesthetic is given. Group 1: Local anesthetic mixture will be given to the corner pocket - where the artery and the first rib intersect in the sonoanatomical image. Group 2: 10 ml of the local anesthetic mixture will be given to the described corner pack and the remaining 10 ml into the largest nerve cluster (Intracluster injection). Group 3: Local anesthetic mixture will be administered by multi injection method between the nerve groups seen in the sonoanatomical image.
Masking
ParticipantOutcomes Assessor
Masking Description
The participant will not know which group he or she is in. The diaphragm thickening fraction and evaluations (outcomes) will be made by another experienced anesthesiologist, double-blindness will be achieved by being blind to the patient's group. Block evaluation and measurements will be made by a different experienced anesthesiologist .
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
corner pocket
Arm Type
Experimental
Arm Description
The block will be performed by an experienced anesthesiologist in block applications under USG guidance. After the antisepsis of the area to be blocked, a 22G 50 mm stimulator needle will be used for the block . Intermittent negative aspiration will be performed during all procedures to detect possible vascular puncture. 20 ml of bupivacaine(Buvicaine HCl %0.5) and prilocaine(Priloc HCl %2) 1:1 mixture will be prepared in a way that there will be 5mcg adrenaline per ml.(9ml bupivacaine, 9ml prilocaine and 2ml saline with 50 mcg adrenaline per ml) Local anesthetic mixture will be given to the corner pocket - where the artery and the first rib intersect in the sonoanatomical image.
Arm Title
corner+intracluster
Arm Type
Experimental
Arm Description
The block will be performed by an experienced anesthesiologist in block applications under USG guidance. After the antisepsis of the area to be blocked, a 22G 50 mm stimulator needle will be used for the block . Intermittent negative aspiration will be performed during all procedures to detect possible vascular puncture20 ml of bupivacaine(Buvicaine HCl %0.5) and prilocaine(Priloc HCl %2) 1:1 mixture will be prepared in a way that there will be 5mcg adrenaline per ml.(9ml bupivacaine, 9ml prilocaine and 2ml saline with 50 mcg adrenaline per ml) 10 ml of the local anesthetic mixture will be given to the described corner pack and the remaining 10 ml into the largest nerve cluster (Intracluster injection).
Arm Title
multi
Arm Type
Experimental
Arm Description
The block will be performed by an experienced anesthesiologist in block applications under USG guidance. After the antisepsis of the area to be blocked, a 22G 50 mm stimulator needle will be used for the block . Intermittent negative aspiration will be performed during all procedures to detect possible vascular puncture. 20 ml of bupivacaine(Buvicaine HCl %0.5) and prilocaine(Priloc HCl %2) 1:1 mixture will be prepared in a way that there will be 5mcg adrenaline per ml.(9ml bupivacaine, 9ml prilocaine and 2ml saline with 50 mcg adrenaline per ml) Local anesthetic mixture will be administered by multi injection method between the nerve groups seen in the sonoanatomical image.
Intervention Type
Drug
Intervention Name(s)
Bupivacaine HCl 0.5% Injectable Solution
Other Intervention Name(s)
buvicaine %0.5,
Intervention Description
20 ml of bupivacaine(Buvicaine HCl %0.5) and prilocaine(Priloc HCl %2) 1:1 mixture will be prepared in a way that there will be 5mcg adrenaline per ml.(9ml bupivacaine, 9ml prilocaine and 2ml saline with 50 mcg adrenaline per ml)
Intervention Type
Drug
Intervention Name(s)
Prilocaine HCl % 2 injectable solution
Other Intervention Name(s)
priloc %2
Intervention Description
20 ml of bupivacaine(Buvicaine HCl %0.5) and prilocaine(Priloc HCl %2) 1:1 mixture will be prepared in a way that there will be 5mcg adrenaline per ml.(9ml bupivacaine, 9ml prilocaine and 2ml saline with 50 mcg adrenaline per ml)
Intervention Type
Drug
Intervention Name(s)
adrenaline amp 0.5mg
Other Intervention Name(s)
adrenalin codex 0.5mg/1ml injectable solution
Intervention Description
20 ml of bupivacaine(Buvicaine HCl %0.5) and prilocaine(Priloc HCl %2) 1:1 mixture will be prepared in a way that there will be 5mcg adrenaline per ml.(9ml bupivacaine, 9ml prilocaine and 2ml saline with 50 mcg adrenaline per ml)
Intervention Type
Procedure
Intervention Name(s)
Ultrasound Guided Supraclavicular Block Corner pocket approach
Intervention Description
The blocks will be performed by an experienced anesthesiologist with a USG guidance. Local anesthetic mixture will be given to the corner pocket - where the artery and the first rib intersect in the sonoanatomical image.
Intervention Type
Procedure
Intervention Name(s)
Ultrasound Guided Supraclavicular Block Corner pocket + intracluster approach
Intervention Description
The blocks will be performed by an experienced anesthesiologist with a USG guidance .10 ml of the local anesthetic mixture will be given to the described corner pack and the remaining 10 ml into the largest nerve cluster (Intracluster injection).
Intervention Type
Procedure
Intervention Name(s)
Ultrasound Guided Supraclavicular Block multi approach
Intervention Description
The blocks will be performed by an experienced anesthesiologist with a USG guidance Local anesthetic mixture will be administered by multi injection method between the nerve groups seen in the sonoanatomical image.
Intervention Type
Procedure
Intervention Name(s)
diagraphma muscle evaluation with ultrasound
Intervention Description
All patients will be evaluated with USG in a head-up position facing the side to be operated before and 30 minutes after the block is performed. The probe will be placed perpendicular to the chest wall, in the eighth or ninth intercostal space, between the anterior axillary and midaxillary lines, 0.5 to 2 cm below the costophrenic sinus.
Primary Outcome Measure Information:
Title
Comparison of Three Different Approach for Supraclavicular Blocks Effects on Diaphragm Thickening Fraction
Description
Several diaphragm images will be taken, at least three at the point of maximum thickening in TLC and at least three at minimum thickness in RV. On each B-mode image, diaphragm thickness will be measured from the middle of the pleural line to the middle of the peritoneal line. Then DTI will be calculated as a percentage from the formula: (Max thickness at the end of inspiration - Max thickness at the end of the expiration) / Max thickness at the end of the expiration. All patients will be evaluated with USG in a head-up position facing the side to be operated 30 minutes after the block is performed.
Time Frame
Comparison of Diaphragm Thickening Fraction will be evaluated 30 minutes after the block is performed.
Secondary Outcome Measure Information:
Title
The sensory block level
Description
Sensory block level; The level of block that will occur in the sensory areas of axillary, median, radial, ulnar, musculocutaneous, cutaneous brachia and cutaneous antebraki medialis nerves will be evaluated by performing a pinprick test and its level will be recorded (0 = Painful, no block; 1 = Partial block-analgesia, only feeling of touch; 2 = Complete block, no pain).
Time Frame
Following the block operation, the sensory block level will be recorded at the 5th, 10th, 15th, 20th, 25th and 30th minutes
Title
The motor block level
Description
It will be evaluated with the Modified Bromage scale: 0 = No blocks, he can lift his arm, 1= Motor power is low but the arm is movable, 2 = The arm is immobile but the fingers are movable, 3 = Complete block, no movement in hand or arm
Time Frame
Following the block operation, the motor block level will be recorded at the 5th, 10th, 15th, 20th, 25th and 30th minutes
Title
Block success
Description
It will be defined as the presence of the pinprick test in the musculacutaneous, radial, ulnar, median, cutaneous antebraki nerves with no pain or only feeling of touch. If any of these nerves are not blocked, it will be considered a failed block.
Time Frame
At the 30th minute of LA application,
Title
Postoperative analgesia time
Description
Numeric rating scale; patient values pain between 0 and 10; 0 = No pain-10 = Intractable pain
Time Frame
The hour when NRS> 1 in the first 24 hours will be recorded.
Title
Pain Score Follow-up
Description
Numeric rating scale; patient values pain between 0 and 10; 0 = No pain-10 = Intractable pain
Time Frame
2nd, 6th, 12th and 24th hours
Title
Block return time
Description
Sensory (the time from local anesthetic injection until the patient fully perceives the upper limb) and motor (the time from local anesthetic injection to the moment the patient's upper limb regains muscle strength) will be recorded as the time to return the block.
Time Frame
The return time of sensory and motor block will be recorded within the first 24 hours.
Title
Block application time
Description
It will be defined as the time from the moment the needle passes through the skin until the local anesthetic is given and the needle is withdraw.
Time Frame
intraoperative (during block application)
Title
Block onset time
Description
It will be defined as the time required to initiate anesthesia and analgesia in all 5 distal nerves from the local anesthetic injection.
Time Frame
baseline (before surgery)
Title
Patient and surgeon satisfaction
Description
Patient and surgeon satisfaction will be evaluated as: 1 = Complete dissatisfaction, 2 = Moderate satisfaction, 3 = Full satisfaction after the procedure.
Time Frame
immediately after the surgery
Title
Undesirable side effects:
Description
Recorded when there is vascular puncture, hematoma, signs of LA toxicity, respiratory distress, pneumothorax, and Horner Syndrome.
Time Frame
Patients will be observed for 24 hours,
Title
The first opioid requirement hour
Description
The first hour of opioid requirement of the patients will be recorded.(When NRS> 3) Opioids(Tramadol) will be administered to patients in case demanded.
Time Frame
If pain occurs within the first 24 hours from the time the block transaction ends.
Title
24-hour total opioid consumption
Description
It will be recorded how much opioid he needs to use for 24 hours.Opioids(Tramadol) will be administered to patients in case demanded.
Time Frame
It will be defined as 24 hours from the time the block transaction ends.
Title
Chronic pain questionnaire
Description
After 6 months, patients will be called and questioned by phone.
Time Frame
6 months after operation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients who are scheduled scheduled for hand, wrist, forearm, arm surgery Patients who has informed consent for study Patients with American Society of Anesthesiologists Physical Status Classification(ASA) I,II and III Exclusion Criteria: Patient's refusal to participate Patients under 18 years of age Patients with known local anesthetic allergy Patients with Body mass index> 35 Patients diagnosed sepsis and bacteriemia, Skin infection at the injection site, History of coagulopathy or anticoagulant therapy Patients with uncontrolled diabetes, Uncoordinated patients, Psychological and emotional lability, Patients with anatomical disorders at application points Pregnant patients
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Çağrı Yeşilnacar, MD
Organizational Affiliation
Izmir Bozyaka Training and Research Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Zeki T Tekgül, Assoc Prof
Organizational Affiliation
Izmir Bozyaka Training and Research Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
AYSUN A KAR, MD
Organizational Affiliation
Izmir Bozyaka Training and Research Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
TAŞKIN ALTAY, Assoc Prof
Organizational Affiliation
Izmir Bozyaka Training and Research Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Izmir Bozyaka Training and Research Hospital
City
İzmir
State/Province
Karabaglar
ZIP/Postal Code
35170
Country
Turkey

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24949192
Citation
Ferrari G, De Filippi G, Elia F, Panero F, Volpicelli G, Apra F. Diaphragm ultrasound as a new index of discontinuation from mechanical ventilation. Crit Ultrasound J. 2014 Jun 7;6(1):8. doi: 10.1186/2036-7902-6-8. eCollection 2014.
Results Reference
background
PubMed Identifier
25650633
Citation
Petrar SD, Seltenrich ME, Head SJ, Schwarz SK. Hemidiaphragmatic paralysis following ultrasound-guided supraclavicular versus infraclavicular brachial plexus blockade: a randomized clinical trial. Reg Anesth Pain Med. 2015 Mar-Apr;40(2):133-8. doi: 10.1097/AAP.0000000000000215.
Results Reference
background
PubMed Identifier
19916254
Citation
Renes SH, Spoormans HH, Gielen MJ, Rettig HC, van Geffen GJ. Hemidiaphragmatic paresis can be avoided in ultrasound-guided supraclavicular brachial plexus block. Reg Anesth Pain Med. 2009 Nov-Dec;34(6):595-9. doi: 10.1097/aap.0b013e3181bfbd83.
Results Reference
background

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Comparison of Different Approaches for Supraclavicular Block and Their Effects on Diaphragm Muscle Function

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