search
Back to results

MORphine Use in the Fascia Iliaca Compartment Block With UltraSound (MORFICUS)

Primary Purpose

Humans, Anesthetics, Local, Morphine

Status
Terminated
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
Levobupivacaine
Placebo
Acetaminophen
Morphine
Fascia Iliaca Compartment Block with Levobupivacaine
Fascia Iliaca Compartment Block with placebo
Sponsored by
Zuyderland Medisch Centrum
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Humans focused on measuring Fascia Iliaca Compartment Block, Peripheral Nerve Block, Elderly, Hip fracture, Levobupivacaïne, Morphine, Emergency Physician, Emergency department, Ultrasound, Pain score, Numerical Rating scale

Eligibility Criteria

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

Inclusion Criteria:

  • Patient diagnosed with a proximal femoral fracture (femoral neck, trochanteric and sub trochanteric femoral fracture) upon arrival at the ED.

Exclusion Criteria:

  1. No informed consent patient
  2. Skin infection at injection site(s)
  3. Morphine allergy
  4. Levobupivacaïne allergy
  5. Operation within an hour after admission
  6. Inability to understand and quantify pain on a NRS
  7. History of dementia
  8. Neurological deficit of fractured leg upon arrival at the ED
  9. Trauma with multiple fractures (more than 1)
  10. Risk of compartment syndrome of ipsilateral lower leg
  11. Proximal femoral fracture with other definitive treatment than operation
  12. Transfer to another hospital
  13. Actual morphine use
  14. Distracting pain in other location than hip
  15. Pregnancy
  16. No physician/nurse available for procedure.
  17. BMI > 40
  18. Saturation < 90%
  19. Previously unreported hypotension (systolic blood pressure < 100 mmHg)
  20. ASA IV or higher

Sites / Locations

  • Zuyderland Medisch Centrum

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Levobupivacaïne

Placebo

Arm Description

Fascia Iliaca Compartment Block with Levobupivacaine Hydrochloride (weight based dosage and volume) Ideal Body Weight : Levobupivacaïne dose (mg) : Dose/kilogram (mg/kg) : Total volume (ml) [<64 kg : 100 mg : 2.0 mg/kg : 40 ml] [65-74 kg : 125 mg : 1.9 mg/kg : 45 ml] [≥ 75 kg : 150 mg : 2.0 mg/kg : 50 ml] Acetaminophen 1 gram (tablets) 4 times daily. Patient Controlled Analgesia Pump with morphine 1 milligram per dose.

Fascia Iliaca Compartment Block with placebo (Sodium Chloride 0.9%), similar volume to experimental arm. Ideal Body Weight : Total volume (ml) [<64 kg : 40 ml] [65-74 kg : 45 ml] [≥ 75 kg : 50 ml] Acetaminophen 1 gram (tablets) 4 times daily. Patient Controlled Analgesia Pump with morphine 1 milligram per dose.

Outcomes

Primary Outcome Measures

Mean morphine consumption in milligrams per hour with PCA pump, extracted from PCA-pump memory (mg / hour).
The primary objective is to assess if ultrasound guided FICB with levobupivacaïne results in reduced morphine consumption in ED patients with a proximal femoral fracture at six hours after FICB placement. The morphine consumption will be extracted from the memory from the PCA pump.

Secondary Outcome Measures

Morphine consumption in milligrams per hour at each hour in the time preceding operation. (mg / hour)
To assess if there is a difference in morphine consumption at different time points in the time until operation. Data will be extracted from PCA pump memory.
Average of PCA-pump requests for morphine per hour (presses / hour)
The amount of times per hour a patient presses the PCA-pump to receive a bolus of morphine preoperatively.
Average time to first morphine administration with PCA-pump (minutes)
Average time until patient requests first morphine dose by pressing PCA-pump button.
Average pain score at different time points.
Pain scores will be reported with the Numerical Rating Scale (NRS). The NRS is a 11 point scale that is used in the hospital pain protocol. 0 equals to no pain at all, 10 is the worst pain one can imagine. It is regarded as a reliable instrument for pain assessment in patients. Patients will be asked to keep track of their pain score at different time points, starting after FICB placement. They will be asked to report their pain score hourly until 22.00h and from 7.00h the next day. The pain scores will be measured with a dedicated android application, with which patients are asked to self-report their hourly pain scores. When patients are asleep no NRS will be recorded, unless they are awake. Also nurses will report pain scores following their normal rounds when changing shifts. A sleeping patient will be regarded as having a low pain score.
Difference in pain scores at movement.
The ED or ward nurse will ask and record the NRS when mobilising patients when necessary. Such situations include for example: bedpan for micturition or stools and bed to bed transfer. The recorded data will include time point, situation and NRS. Pain scores will be reported with the Numerical Rating Scale (NRS). The NRS is a 11 point scale that is used in the hospital pain protocol. 0 equals to no pain at all, 10 is the worst pain one can imagine.
Patients with occurence of NRS > 3.
The number of patient with a NRS > 3, recorded by the patient in the preoperative time.
Number of patients with a delirium in preoperative period.
The Delirium Observation Screening (DOS) scale is a validated screening tool for detecting delirium in hospitalised patients. In this hospital the DOS scale is routinely screened three times daily by ward nurses. The DOS will also be reported for participating patients in the preoperative period. Subjects with a reported DOS of ≥ 3 are regarded as being at high risk for having a delirium.
The number of patients with morphine related side effects.
A patient will be regarded of having a side effect of morphine in case of any of the following: Occurrence of nausea Occurrence of vomiting Administration of antiemetic medication Episode of respiratory depression (< 10 breaths/minute) Episode of new hypoxia (SaO2 < 90 % ) Administration of naloxone, which will be registered by the nurse on the CRF. Episodes of new hypotension. In this trial hypotension is defined as a systolic blood pressure <90 mmHg, mean arterial pressure <60 mmHg or a drop in systolic blood pressure >40 mmHg. Sedation score > 1. This wil be reported by the nurse with the Pasero Opioïd Induced Sedation Scale, as is prescribed by hospital protocol. S = normal sleep, 1 = drowsy but easy to rouse, 2 = sedated and difficult to rouse, and 3 = unconscious).
Number of patients with treatment-related adverse events as assessed by CTCAE v4.0.
Adverse events relating to the fascia iliaca compartment block or morphine use will be reported.
Time spent on FICB placement in seconds.
The duration of ultrasound guided FICB placement will be measured.

Full Information

First Posted
February 7, 2019
Last Updated
May 3, 2021
Sponsor
Zuyderland Medisch Centrum
Collaborators
Fresenius Kabi
search

1. Study Identification

Unique Protocol Identification Number
NCT03846102
Brief Title
MORphine Use in the Fascia Iliaca Compartment Block With UltraSound
Acronym
MORFICUS
Official Title
MORphine Use in the Fascia Iliaca Compartment Block With UltraSound
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Terminated
Why Stopped
COVID-19 crisis.
Study Start Date
January 28, 2019 (Actual)
Primary Completion Date
February 18, 2020 (Actual)
Study Completion Date
February 18, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Zuyderland Medisch Centrum
Collaborators
Fresenius Kabi

4. Oversight

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

5. Study Description

Brief Summary
Appropriate management of analgesia for proximal femoral fractures is a common problem in the emergency department (ED). Side effects from morphine usage such as nausea, vomiting, respiratory depression, sedation, and obstipation are especially pronounced in elderly. Fascia Iliaca Compartment Block (FICB) holds promise as a simple and safe, and effective alternative method to reduce pain. Local anaesthetic injected in the anatomic space underlying the fascia iliaca, spreads to block the nerves traversing it. This regional anaesthesia includes the femoral nerve. Previous studies in the ED showed promise but lacked blinding, involved low numbers of subjects, or did not use ultrasound localisation of the injection site. The latter is becoming common practice. In this randomised placebo controlled trial the FICB with ultrasound localisation of injection of levobupivacaïne will be compared to the FICB with placebo. It aims to prove that less morphine is used in the intervention group. Other research parameters are pain scores and minor adverse events related to morphine use.
Detailed Description
Proximal femoral fractures are common in the ED. A major challenge in such subjects is pain management. Suboptimal pain control is associated with stress, a prolonged hospital stay and delirium. Pain or fear of pain can limit early mobilisation, an important goal in treatment. Therefore early pain management is essential. Standard analgesic care consists of acetaminophen, opiates and/or Non-steroidal anti-inflammatory drugs (NSAID's). Opiates can cause respiratory depression, constipation, drowsiness, nausea and vomiting. Especially elderly patients are at risk for these side effects Regional nerve blocks are increasingly being adopted as an alternative pain management to systemic analgesia in the ED. One of such is the Fascia Iliaca Compartment Block (FICB). This is safe and simple to perform. Results from studies, despite lacking ultrasound guidance are promising. No permanent disability resulted from the few minor complications that have been reported. These include bladder perforation, pneumoretroperitoneum and neuropathy of the femoral nerve. Furthermore no additional treatment was necessary. Ultrasound prevents occurrence of such complications. The studies that have compared this specific block to standard analgesia have shown that regional anaesthesia may be superior. However these studies have low inclusion numbers and lack of randomisation and/or blinding.. Literature up until now has used the numerical rating scale (NRS) as a primary outcome. Although the NRS is a very trustworthy method of measuring pain, the score is a subjective outcome Morphine consumption on the other hand is more objective. The FICB involves the anatomic space situated at the level of the groin in which important nerves that supply the hip joint lie. Anteriorly the space is covered by the iliac fascia. It is therefore known as the fascia iliaca compartment. By introducing a large volume of local anaesthetic solutions, the femoral, lateral femoral cutaneous and to a lesser extent the obturator nerve are anesthetized. Solutions can spread easily within the compartment. Therefore a safe position injection site can be chosen, minimizing the risk of intravascular injection and nerve damage. The classic position for injection is about 3 centimetres lateral from the femoral nerve. In the original FICB the injection site is determined by using landmarks. The fascia iliaca compartment is then approached by introducing a blunt needle, which enables the physician to feel a 'pop' twice. The first pop is felt when the fascia lata is pierced, the second when the fascia iliaca is passed. Most ED's nowadays have access to ultrasound. When used for FICB placement, the local anaesthetic solution is visualized as it is introduced into the space. Therefore a higher chance of successful placement of agent and a lower risk of complications can be expected. So far no large double blind randomised placebo controlled trials have evaluated morphine use in ultrasound guided placement of local anaesthetic agents with FICB in the ED. This study is designed as such. Total morphine use will be taken as the primary outcome, administered in the form of patient controlled analgesia (PCA).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Humans, Anesthetics, Local, Morphine, Pain Management, Analgesia, Pain, Anesthesia, Local, Fascia, Emergency Medicine, Analgesia, Patient-Controlled, Ultrasonography, Femoral Fracture
Keywords
Fascia Iliaca Compartment Block, Peripheral Nerve Block, Elderly, Hip fracture, Levobupivacaïne, Morphine, Emergency Physician, Emergency department, Ultrasound, Pain score, Numerical Rating scale

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
double-blinded randomized placebo-controlled trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Syringes with either placebo or levobupivacaïne will be prepared under aseptic conditions and blinded by the hospital pharmacy. A supply of at least six syringe packs will be kept in the emergency department. Each pack will contain three different doses of either levobupivacain or placebo, of which one will be used according to the weight of the patient. When medication is used, the nurse, physician or researcher will inform the pharmacy, so new medication can be prepared. The hospital pharmacy will keep track of randomisation and register the allocation to either treatment or placebo. Allocation will remain blinded until all patients are included and all data is included.
Allocation
Randomized
Enrollment
55 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Levobupivacaïne
Arm Type
Experimental
Arm Description
Fascia Iliaca Compartment Block with Levobupivacaine Hydrochloride (weight based dosage and volume) Ideal Body Weight : Levobupivacaïne dose (mg) : Dose/kilogram (mg/kg) : Total volume (ml) [<64 kg : 100 mg : 2.0 mg/kg : 40 ml] [65-74 kg : 125 mg : 1.9 mg/kg : 45 ml] [≥ 75 kg : 150 mg : 2.0 mg/kg : 50 ml] Acetaminophen 1 gram (tablets) 4 times daily. Patient Controlled Analgesia Pump with morphine 1 milligram per dose.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Fascia Iliaca Compartment Block with placebo (Sodium Chloride 0.9%), similar volume to experimental arm. Ideal Body Weight : Total volume (ml) [<64 kg : 40 ml] [65-74 kg : 45 ml] [≥ 75 kg : 50 ml] Acetaminophen 1 gram (tablets) 4 times daily. Patient Controlled Analgesia Pump with morphine 1 milligram per dose.
Intervention Type
Drug
Intervention Name(s)
Levobupivacaine
Other Intervention Name(s)
Chirocaïne, Levobupivacaine Hydrochloride
Intervention Description
Levobupivacaïne for injection 7.5 mg/kg diluted with Sodium Chloride 0,9%
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Placebo (for levobupivacaïne)
Intervention Description
Sodium Chloride 0,9% for injection/infusion.
Intervention Type
Drug
Intervention Name(s)
Acetaminophen
Other Intervention Name(s)
Paracetamol
Intervention Description
Acetaminophen 500 milligram tablet
Intervention Type
Drug
Intervention Name(s)
Morphine
Other Intervention Name(s)
Morphine hydrochloride
Intervention Description
Morphine 1 mg/ml solution for infusion.
Intervention Type
Procedure
Intervention Name(s)
Fascia Iliaca Compartment Block with Levobupivacaine
Other Intervention Name(s)
Fascia Iliaca Compartment Block, FIC Block
Intervention Description
Ultrasound guided Fascia Iliaca Compartment Block with levobupivacaine placed in the emergency department by an emergency physician.
Intervention Type
Procedure
Intervention Name(s)
Fascia Iliaca Compartment Block with placebo
Other Intervention Name(s)
Fascia Iliaca Compartment Block, FIC Block
Intervention Description
Ultrasound guided Fascia Iliaca Compartment Block with placebo placed in the emergency department by an emergency physician.
Primary Outcome Measure Information:
Title
Mean morphine consumption in milligrams per hour with PCA pump, extracted from PCA-pump memory (mg / hour).
Description
The primary objective is to assess if ultrasound guided FICB with levobupivacaïne results in reduced morphine consumption in ED patients with a proximal femoral fracture at six hours after FICB placement. The morphine consumption will be extracted from the memory from the PCA pump.
Time Frame
From FICB placement up to 6 hours.
Secondary Outcome Measure Information:
Title
Morphine consumption in milligrams per hour at each hour in the time preceding operation. (mg / hour)
Description
To assess if there is a difference in morphine consumption at different time points in the time until operation. Data will be extracted from PCA pump memory.
Time Frame
Time from FICB placement until operation, up to 24 hours. Time point: each hour
Title
Average of PCA-pump requests for morphine per hour (presses / hour)
Description
The amount of times per hour a patient presses the PCA-pump to receive a bolus of morphine preoperatively.
Time Frame
Time from FICB placement until operation, up to 24 hours. Time point: each hour
Title
Average time to first morphine administration with PCA-pump (minutes)
Description
Average time until patient requests first morphine dose by pressing PCA-pump button.
Time Frame
Time from FICB placement until operation, up to 24 hours.
Title
Average pain score at different time points.
Description
Pain scores will be reported with the Numerical Rating Scale (NRS). The NRS is a 11 point scale that is used in the hospital pain protocol. 0 equals to no pain at all, 10 is the worst pain one can imagine. It is regarded as a reliable instrument for pain assessment in patients. Patients will be asked to keep track of their pain score at different time points, starting after FICB placement. They will be asked to report their pain score hourly until 22.00h and from 7.00h the next day. The pain scores will be measured with a dedicated android application, with which patients are asked to self-report their hourly pain scores. When patients are asleep no NRS will be recorded, unless they are awake. Also nurses will report pain scores following their normal rounds when changing shifts. A sleeping patient will be regarded as having a low pain score.
Time Frame
Time from FICB placement until operation, up to 24 hours. Time point: each hour
Title
Difference in pain scores at movement.
Description
The ED or ward nurse will ask and record the NRS when mobilising patients when necessary. Such situations include for example: bedpan for micturition or stools and bed to bed transfer. The recorded data will include time point, situation and NRS. Pain scores will be reported with the Numerical Rating Scale (NRS). The NRS is a 11 point scale that is used in the hospital pain protocol. 0 equals to no pain at all, 10 is the worst pain one can imagine.
Time Frame
Time from FICB placement until operation, up to 24 hours. Time point: each hour
Title
Patients with occurence of NRS > 3.
Description
The number of patient with a NRS > 3, recorded by the patient in the preoperative time.
Time Frame
Time from FICB placement until operation, up to 24 hours. Time point at 24 hours.
Title
Number of patients with a delirium in preoperative period.
Description
The Delirium Observation Screening (DOS) scale is a validated screening tool for detecting delirium in hospitalised patients. In this hospital the DOS scale is routinely screened three times daily by ward nurses. The DOS will also be reported for participating patients in the preoperative period. Subjects with a reported DOS of ≥ 3 are regarded as being at high risk for having a delirium.
Time Frame
Time from FICB placement until operation, up to 24 hours. Time point at 24 hours.
Title
The number of patients with morphine related side effects.
Description
A patient will be regarded of having a side effect of morphine in case of any of the following: Occurrence of nausea Occurrence of vomiting Administration of antiemetic medication Episode of respiratory depression (< 10 breaths/minute) Episode of new hypoxia (SaO2 < 90 % ) Administration of naloxone, which will be registered by the nurse on the CRF. Episodes of new hypotension. In this trial hypotension is defined as a systolic blood pressure <90 mmHg, mean arterial pressure <60 mmHg or a drop in systolic blood pressure >40 mmHg. Sedation score > 1. This wil be reported by the nurse with the Pasero Opioïd Induced Sedation Scale, as is prescribed by hospital protocol. S = normal sleep, 1 = drowsy but easy to rouse, 2 = sedated and difficult to rouse, and 3 = unconscious).
Time Frame
This will be assessed by the nurse at the rounds each shift up to 3 times daily until operation or up to 24 hours.
Title
Number of patients with treatment-related adverse events as assessed by CTCAE v4.0.
Description
Adverse events relating to the fascia iliaca compartment block or morphine use will be reported.
Time Frame
Time from FICB placement until operation, up to 24 hours.
Title
Time spent on FICB placement in seconds.
Description
The duration of ultrasound guided FICB placement will be measured.
Time Frame
The time from needle entering patient, until procedure is terminated by the emergency physician.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient diagnosed with a proximal femoral fracture (femoral neck, trochanteric and sub trochanteric femoral fracture) upon arrival at the ED. Exclusion Criteria: No informed consent patient Skin infection at injection site(s) Morphine allergy Levobupivacaïne allergy Operation within an hour after admission Inability to understand and quantify pain on a NRS History of dementia Neurological deficit of fractured leg upon arrival at the ED Trauma with multiple fractures (more than 1) Risk of compartment syndrome of ipsilateral lower leg Proximal femoral fracture with other definitive treatment than operation Transfer to another hospital Actual morphine use Distracting pain in other location than hip Pregnancy No physician/nurse available for procedure. BMI > 40 Saturation < 90% Previously unreported hypotension (systolic blood pressure < 100 mmHg) ASA IV or higher
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sanne Postma, MD
Organizational Affiliation
Zuyderland Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zuyderland Medisch Centrum
City
Heerlen
State/Province
Zuid Limburg
ZIP/Postal Code
6419PC
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
9862240
Citation
Hughes SG. Prescribing for the elderly patient: why do we need to exercise caution? Br J Clin Pharmacol. 1998 Dec;46(6):531-3. doi: 10.1046/j.1365-2125.1998.00842.x. No abstract available.
Results Reference
result
PubMed Identifier
11331334
Citation
Cherny N, Ripamonti C, Pereira J, Davis C, Fallon M, McQuay H, Mercadante S, Pasternak G, Ventafridda V; Expert Working Group of the European Association of Palliative Care Network. Strategies to manage the adverse effects of oral morphine: an evidence-based report. J Clin Oncol. 2001 May 1;19(9):2542-54. doi: 10.1200/JCO.2001.19.9.2542.
Results Reference
result
PubMed Identifier
18686750
Citation
Chau DL, Walker V, Pai L, Cho LM. Opiates and elderly: use and side effects. Clin Interv Aging. 2008;3(2):273-8. doi: 10.2147/cia.s1847.
Results Reference
result
PubMed Identifier
14622770
Citation
Wheeler M, Oderda GM, Ashburn MA, Lipman AG. Adverse events associated with postoperative opioid analgesia: a systematic review. J Pain. 2002 Jun;3(3):159-80. doi: 10.1054/jpai.2002.123652. No abstract available.
Results Reference
result
PubMed Identifier
26759680
Citation
Groot L, Dijksman LM, Simons MP, Zwartsenburg MM, Rebel JR. Single Fascia Iliaca Compartment Block is Safe and Effective for Emergency Pain Relief in Hip-fracture Patients. West J Emerg Med. 2015 Dec;16(7):1188-93. doi: 10.5811/westjem.2015.10.28270. Epub 2015 Dec 14.
Results Reference
result
PubMed Identifier
26330019
Citation
Ritcey B, Pageau P, Woo MY, Perry JJ. Regional Nerve Blocks For Hip and Femoral Neck Fractures in the Emergency Department: A Systematic Review. CJEM. 2016 Jan;18(1):37-47. doi: 10.1017/cem.2015.75. Epub 2015 Sep 2.
Results Reference
result
PubMed Identifier
27714758
Citation
Kearns R, Macfarlane A, Grant A, Puxty K, Harrison P, Shaw M, Anderson K, Kinsella J. A randomised, controlled, double blind, non-inferiority trial of ultrasound-guided fascia iliaca block vs. spinal morphine for analgesia after primary hip arthroplasty. Anaesthesia. 2016 Dec;71(12):1431-1440. doi: 10.1111/anae.13620. Epub 2016 Oct 7.
Results Reference
result
PubMed Identifier
22506940
Citation
Birnbaum A, Schechter C, Tufaro V, Touger R, Gallagher EJ, Bijur P. Efficacy of patient-controlled analgesia for patients with acute abdominal pain in the emergency department: a randomized trial. Acad Emerg Med. 2012 Apr;19(4):370-7. doi: 10.1111/j.1553-2712.2012.01322.x.
Results Reference
result
PubMed Identifier
11472277
Citation
Walder B, Schafer M, Henzi I, Tramer MR. Efficacy and safety of patient-controlled opioid analgesia for acute postoperative pain. A quantitative systematic review. Acta Anaesthesiol Scand. 2001 Aug;45(7):795-804. doi: 10.1034/j.1399-6576.2001.045007795.x.
Results Reference
result
PubMed Identifier
12411815
Citation
Auroy Y, Benhamou D, Bargues L, Ecoffey C, Falissard B, Mercier FJ, Bouaziz H, Samii K. Major complications of regional anesthesia in France: The SOS Regional Anesthesia Hotline Service. Anesthesiology. 2002 Nov;97(5):1274-80. doi: 10.1097/00000542-200211000-00034. Erratum In: Anesthesiology. 2003 Feb;98(2):595. Mercier Frederic [corrected to Mercier Frederic J].
Results Reference
result
PubMed Identifier
19157368
Citation
Blackford D, Westhoffen P. Accidental bladder puncture: a complication of a modified fascia iliaca block. Anaesth Intensive Care. 2009 Jan;37(1):140-1. No abstract available.
Results Reference
result
PubMed Identifier
11374619
Citation
Atchabahian A, Brown AR. Postoperative neuropathy following fascia iliaca compartment blockade. Anesthesiology. 2001 Mar;94(3):534-6. doi: 10.1097/00000542-200103000-00029. No abstract available.
Results Reference
result
PubMed Identifier
17138203
Citation
Shelley BG, Haldane GJ. Pneumoretroperitoneum as a consequence of fascia iliaca block. Reg Anesth Pain Med. 2006 Nov-Dec;31(6):582-3. doi: 10.1016/j.rapm.2006.08.009. No abstract available.
Results Reference
result
PubMed Identifier
23788067
Citation
Barrington MJ, Kluger R. Ultrasound guidance reduces the risk of local anesthetic systemic toxicity following peripheral nerve blockade. Reg Anesth Pain Med. 2013 Jul-Aug;38(4):289-99. doi: 10.1097/AAP.0b013e318292669b.
Results Reference
result
PubMed Identifier
27787895
Citation
Morrison RS, Dickman E, Hwang U, Akhtar S, Ferguson T, Huang J, Jeng CL, Nelson BP, Rosenblatt MA, Silverstein JH, Strayer RJ, Torrillo TM, Todd KH. Regional Nerve Blocks Improve Pain and Functional Outcomes in Hip Fracture: A Randomized Controlled Trial. J Am Geriatr Soc. 2016 Dec;64(12):2433-2439. doi: 10.1111/jgs.14386. Epub 2016 Oct 27.
Results Reference
result
PubMed Identifier
12560416
Citation
Morrison RS, Magaziner J, Gilbert M, Koval KJ, McLaughlin MA, Orosz G, Strauss E, Siu AL. Relationship between pain and opioid analgesics on the development of delirium following hip fracture. J Gerontol A Biol Sci Med Sci. 2003 Jan;58(1):76-81. doi: 10.1093/gerona/58.1.m76.
Results Reference
result
PubMed Identifier
23878064
Citation
Rashid A, Beswick E, Galitzine S, Fitton L. Regional analgesia in the emergency department for hip fractures: survey of current UK practice and its impact on services in a teaching hospital. Emerg Med J. 2014 Nov;31(11):909-13. doi: 10.1136/emermed-2013-202794. Epub 2013 Jul 22.
Results Reference
result
PubMed Identifier
2589650
Citation
Dalens B, Vanneuville G, Tanguy A. Comparison of the fascia iliaca compartment block with the 3-in-1 block in children. Anesth Analg. 1989 Dec;69(6):705-13. Erratum In: Anesth Analg 1990 Apr;70(4):474.
Results Reference
result
PubMed Identifier
18762870
Citation
Hogh A, Dremstrup L, Jensen SS, Lindholt J. Fascia iliaca compartment block performed by junior registrars as a supplement to pre-operative analgesia for patients with hip fracture. Strategies Trauma Limb Reconstr. 2008 Sep;3(2):65-70. doi: 10.1007/s11751-008-0037-9. Epub 2008 Sep 2.
Results Reference
result
PubMed Identifier
1015603
Citation
Revill SI, Robinson JO, Rosen M, Hogg MI. The reliability of a linear analogue for evaluating pain. Anaesthesia. 1976 Nov;31(9):1191-8. doi: 10.1111/j.1365-2044.1976.tb11971.x.
Results Reference
result
PubMed Identifier
19174373
Citation
Abrahams MS, Aziz MF, Fu RF, Horn JL. Ultrasound guidance compared with electrical neurostimulation for peripheral nerve block: a systematic review and meta-analysis of randomized controlled trials. Br J Anaesth. 2009 Mar;102(3):408-17. doi: 10.1093/bja/aen384. Epub 2009 Jan 26.
Results Reference
result
PubMed Identifier
11331167
Citation
Huang JJ, Taguchi A, Hsu H, Andriole GL Jr, Kurz A. Preoperative oral rofecoxib does not decrease postoperative pain or morphine consumption in patients after radical prostatectomy: a prospective, randomized, double-blinded, placebo-controlled trial. J Clin Anesth. 2001 Mar;13(2):94-7. doi: 10.1016/s0952-8180(01)00219-7.
Results Reference
result
PubMed Identifier
19690943
Citation
Mouzopoulos G, Vasiliadis G, Lasanianos N, Nikolaras G, Morakis E, Kaminaris M. Fascia iliaca block prophylaxis for hip fracture patients at risk for delirium: a randomized placebo-controlled study. J Orthop Traumatol. 2009 Sep;10(3):127-33. doi: 10.1007/s10195-009-0062-6. Epub 2009 Aug 19.
Results Reference
result
PubMed Identifier
23569691
Citation
Petre BM, Roxbury CR, McCallum JR, Defontes KW 3rd, Belkoff SM, Mears SC. Pain reporting, opiate dosing, and the adverse effects of opiates after hip or knee replacement in patients 60 years old or older. Geriatr Orthop Surg Rehabil. 2012 Mar;3(1):3-7. doi: 10.1177/2151458511432758.
Results Reference
result
PubMed Identifier
12548273
Citation
Fletcher AK, Rigby AS, Heyes FL. Three-in-one femoral nerve block as analgesia for fractured neck of femur in the emergency department: a randomized, controlled trial. Ann Emerg Med. 2003 Feb;41(2):227-33. doi: 10.1067/mem.2003.51.
Results Reference
result
PubMed Identifier
17413915
Citation
Foss NB, Kristensen BB, Bundgaard M, Bak M, Heiring C, Virkelyst C, Hougaard S, Kehlet H. Fascia iliaca compartment blockade for acute pain control in hip fracture patients: a randomized, placebo-controlled trial. Anesthesiology. 2007 Apr;106(4):773-8. doi: 10.1097/01.anes.0000264764.56544.d2.
Results Reference
result
PubMed Identifier
33238043
Citation
Guay J, Kopp S. Peripheral nerve blocks for hip fractures in adults. Cochrane Database Syst Rev. 2020 Nov 25;11(11):CD001159. doi: 10.1002/14651858.CD001159.pub3.
Results Reference
derived
Links:
URL
https://www.anesthesiologie.nl/uploads/files/KD_RL_Neuraxisblokkade.pdf
Description
Guideline anticoagluants and regional anestesia and peripheral nerve blocks of the Dutch Society of Anesthesiology

Learn more about this trial

MORphine Use in the Fascia Iliaca Compartment Block With UltraSound

We'll reach out to this number within 24 hrs