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Guidelines Cefaleia Pos Raqui
Guidelines Cefaleia Pos Raqui
OBJECTIVE To fill the practice guidelines void and provide comprehensive information and patient- Findings In this consensus statement, a
centric recommendations for preventing, diagnosing, and managing PDPH. multidisciplinary panel of 21
collaborators outlined
EVIDENCE REVIEW With input from committee members and stakeholders of 6 participating recommendations for the prevention,
professional societies, 10 review questions that were deemed important for the prevention, identification, and management of
diagnosis, and management of PDPH were developed. A literature search for each question was PDPH. The strength and certainty of
performed in MEDLINE on March 2, 2022. Additional relevant clinical trials, systematic reviews, and evidence of various patient, procedural,
research studies published through March 2022 were also considered for practice guideline diagnostic, and management aspects
development and shared with collaborator groups. Each group submitted a structured narrative of PDPH were graded.
review along with recommendations that were rated according to the US Preventive Services Task
Meaning These practice guidelines
Force grading of evidence. Collaborators were asked to vote anonymously on each recommendation
provide a framework for individual
using 2 rounds of a modified Delphi approach.
clinicians to assess risk, confirm
diagnosis, and adopt a systematic
FINDINGS After 2 rounds of electronic voting by a 21-member multidisciplinary collaborator team,
approach to management of PDPH.
47 recommendations were generated to provide guidance on the risk factors for and the prevention,
diagnosis, and management of PDPH, along with ratings for the strength and certainty of evidence.
A 90% to 100% consensus was obtained for almost all recommendations. Several recommendations + Invited Commentary
were rated as having moderate to low certainty. Opportunities for future research were identified.
+ Supplemental content
Author affiliations and article information are
CONCLUSIONS AND RELEVANCE Results of this consensus statement suggest that current
listed at the end of this article.
approaches to the treatment and management of PDPH are not uniform due to the paucity of
evidence. The practice guidelines, however, provide a framework for individual clinicians to assess
PDPH risk, confirm the diagnosis, and adopt a systematic approach to its management.
Introduction
Postdural puncture headache (PDPH) is a recognized complication of unintentional dural puncture
during epidural analgesia or intentional dural puncture for spinal anesthesia or for diagnostic or
interventional neuraxial procedures. Its incidence varies widely, with rates ranging from less than 2%
to 40% depending on procedural and patient factors.1-3
Open Access. This is an open access article distributed under the terms of the CC-BY License.
JAMA Network Open. 2023;6(8):e2325387. doi:10.1001/jamanetworkopen.2023.25387 (Reprinted) August 15, 2023 1/14
Postdural puncture headache is usually postural and presents within the first 5 days of
witnessed or suspected dural puncture.4 Headache is often accompanied by neck stiffness and/or
subjective hearing symptoms. Although headache may resolve within 2 weeks, its severity may
interfere with daily activities; this severity becomes especially important to postpartum patients
caring for a newborn child. Furthermore, PDPH is associated with complications, including chronic
headache, backache, cranial nerve dysfunction, subdural hematoma (SDH), and cerebral venous
sinus thrombosis (CVST).5
Despite numerous reviews on prevention and management of PDPH, most lacked structured
recommendations. The reason is that their data were inconclusive, as the studies in these reviews
were generally small and heterogeneous, often mixing preventive and therapeutic treatments. In
2013, Bradbury et al6 presented evidence on preventive modalities for PDPH. Subsequently in 2019,
Russell et al7,8 summarized evidence on conservative management and use of an epidural blood
patch (EBP) for PDPH in obstetrics. More recent studies have been added to the current body of
literature.9 Furthermore, there is a lack of practice guidelines for both perioperative and diagnostic
or interventional settings. The current multisociety practice guidelines we developed aimed to fill this
void and provide comprehensive information and patient-centric recommendations for preventing,
diagnosing, and managing PDPH.
Methods
In accordance with the Common Rule, this Consensus Statement was exempt from institutional
review board approval and informed consent because it did not involve human participants or use
identifiable data. We followed the Standards for Quality Improvement Reporting Excellence
(SQUIRE) reporting guideline.
Two of us (V.U., S.N.), the project cochairs, initially obtained approval from the American Society
of Regional Anesthesia and Pain Medicine (ASRA Pain Medicine) guidelines committee and board of
directors. Delegates from the ASRA Pain Medicine, European Society of Regional Anaesthesia and
Pain Therapy, Society for Obstetric Anesthesia and Perinatology, Obstetric Anaesthetists’
Association, American Society of Spine Radiology, and American Interventional Headache Society
were contacted by the ASRA Pain Medicine executive director and invited to contribute to the
development of the present multisociety practice guidelines (Figure). With input from the
committee members and stakeholders, the project cochairs developed 10 review questions that we
deemed important for the prevention, diagnosis, and management of PDPH. After an initial virtual
meeting, collaborators were divided into writing groups, each of which had a designated
group leader.
A health sciences librarian conducted literature searches for each question in MEDLINE ALL on
March 2, 2022. The search block for the term PDPH that was common to all searches was combined
with search blocks that were specific to each review question (eAppendix 1 in the Supplement). Only
English-language articles published after 1960 were included. Animal studies were excluded from
all searches. Results from each search were imported into separate Covidence projects for
deduplication and screening, followed by data extraction. In addition, systematic reviews on PDPH
were searched and shared with collaborators, and references were screened to ensure no essential
references were missed.
Each group submitted a structured narrative review. Key evidence points were summarized as
statements, and practice recommendations were based on the reviewed evidence.
Recommendations were evaluated according to the US Preventive Services Task Force guidelines for
grading of evidence.10 Evidence was graded as A, B, C, D, or I (Table 1), whereas the level of certainty
was rated as high, moderate, or low (Table 2).11 Statements were presented when recommendations
were not possible (eg, for patient factors) or when there was insufficient evidence to make
recommendations. Statements were assigned a certainty level without grading, whereas
recommendations were assigned both level of certainty and grading. The editing team (including
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R.R., V.U., and R.S.) reviewed submissions, which underwent multiple iterations with collaborators to
formulate an interim draft.
The interim draft was shared electronically, with a request to each collaborator to vote
anonymously on each recommendation using a modified Delphi approach.12 We used Microsoft Excel
(Microsoft Corp) for 2 rounds of electronic voting. The Delphi evaluation criteria were simplified, and
collaborators were asked to indicate whether they agreed or disagreed with or would like to abstain
• Each team contributed a • Modified Delphi approach • Recommendations with 100% • Final draft prepared and shared
narrative review used agreement accepted, and with all collaborators AIHS indicates American Interventional Headache
• Drafting of evidence summary • Collaborators requested to recommendations with <100% • Submitted for publication
Society; ASRA, American Society of Regional
from RCTs, cohort studies, vote anonymously on each agreement underwent
case reports, or systematic recommendation voting in round 2 Anesthesia and Pain Medicine; ASSR, American Society
reviews as applicable • Collaborators requested to • Statements and of Spine Radiology; ESRA, European Society of
• Statements or recommendations indicate agreement (agree, recommendations with >75%
agreement were accepted Regional Anaesthesia and Pain Therapy; OAA,
using US Preventive Services disagree, or abstain)
Task Force grading-of-evidence • Mandatory comments and (final draft) Obstetric Anaesthetists’ Association; PDPH, postdural
guideline reasons for decision (if • Language of recommendations puncture headache; RCT, randomized clinical trial;
• Interim draft prepared and disagreed or abstained) was refined with consideration
shared with collaborators of contributors’ comments SOAP, Society for Obstetric Anesthesia and
Perinatology.
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from each recommendation.13 Collaborators were also invited to provide mandatory comments and
reasons for their decision if they disagreed or abstained.
The editing team refined and clarified the statements and recommendations after the first
round of voting. Recommendations with 100% agreement were accepted, and recommendations
with less than 100% agreement were revised with consideration of collaborators’ comments. The
aim was to increase the consensus in the second round of voting. In the second round, the
statements and recommendations with a predefined agreement greater than 75% were accepted.
This threshold was used in another ASRA Pain Medicine consensus guideline.14 The subsequent draft
was shared with all of the collaborators for final approval.
Results
The results retrieved in MEDLINE for each search question are provided in eAppendix 1 in the
Supplement. After 2 rounds of anonymous voting by the 21 multidisciplinary collaborators, the
predefined consensus was greater than 75% for all statements and recommendations. Specifically,
90% to 100% consensus was obtained for almost all recommendations after the second round of
voting (eAppendix 3 in the Supplement). The final draft was approved by each collaborator, the ASRA
Pain Medicine board of directors, and the participating societies. The complete references
supporting each section are provided in eAppendix 2 in the Supplement. The full narrative synthesis
that forms the basis of these recommendations are published elsewhere.15
Definition of PDPH
According to the 2018 definition by the International Headache Society (IHS), PDPH is a headache
attributed to low cerebrospinal fluid (CSF) pressure occurring within 5 days of a lumbar puncture
caused by CSF leakage through the dural puncture.16 Headache is usually accompanied by neck
stiffness and/or subjective hearing symptoms, remitting spontaneously within 2 weeks or after
sealing of the leak with an autologous epidural lumbar patch. As such, this IHS definition requires
evidence of low pressure or CSF leakage on cerebral imaging (showing brain sagging or
pachymeningeal enhancement or extradural CSF).
This definition has several potential weaknesses. First, neither opening nor closing pressure has
been shown to differ in studies of patients with PDPH compared with controls.17,18 Second, patients
with intracranial hypertension can have PDPH.19 Third, case reports and series have shown that
PDPH may become apparent more than 5 days after dural puncture20-22 or after hospital
discharge.23,24 Fourth, the omission of the postural component is controversial. The 2013 IHS
Table 2. US Preventive Services Task Force (USPSTF) Levels of Certainty Regarding Net Benefita
Level of
certaintyb Description
High The available evidence usually includes consistent results from well-designed, well-conducted
studies in representative primary care populations. These studies assess the effects of the preventive
service on health outcomes. This conclusion is therefore unlikely to be strongly affected by the
results of future studies.
Moderate The available evidence is sufficient to determine the effects of the preventive service on health
outcomes, but confidence in the estimate is constrained by such factors as:
• The number, size, or quality of individual studies.
• Inconsistency of findings across individual studies.
• Limited generalizability of findings to routine primary care practice.
• Lack of coherence in the chain of evidence.
a
As more information becomes available, the magnitude or direction of the observed effect could Data from USPSTF.10
change, and this change may be large enough to alter the conclusion. b
“The USPSTF defines certainty as ‘likelihood that the
Low The available evidence is insufficient to assess effects on health outcomes. Evidence is insufficient
USPSTF assessment of the net benefit of a
because of:
• The limited number or size of studies. preventive service is correct.’ The net benefit is
• Important flaws in study design or methods. defined as benefit minus harm of the preventive
• Inconsistency of findings across individual studies.
service as implemented in a general, primary care
• Gaps in the chain of evidence.
• Findings not generalizable to routine primary care practice. population. The USPSTF assigns a certainty level
• Lack of information on important health outcomes. based on the nature of the overall evidence available
More information may allow estimation of effects on health outcomes.
to assess the net benefit of a preventive service.”10
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definition contained a postural component25: “a headache that worsens within 15 minutes after
sitting or standing and improves within 15 minutes after lying down after dural puncture has occurred
or is suspected.” An analysis of the electronic records of 27 064 parturient individuals with a
neuraxial procedure over a 10-year period found that only 8 of 142 parturient individuals with PDPH
had no postural component.4 Fifth, dural puncture may not be noticed during the procedure.26 Sixth,
an increasing body of evidence suggests that headache can persist for longer than 2 weeks.27-31
Question 2: What Patient Factors Are Associated With the Incidence of PDPH?
All statements regarding patient factors are provided in Table 3.34,35 In the statements, younger
adults and female sex were associated with an increased risk of PDPH (level of certainty: high).
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using a cutting needle for lumbar puncture, the use of a narrower-gauge needle is recommended to
reduce the risk of PDPH (evidence grade: A; level of certainty: high).
Third, limited evidence supports the use of narrower-gauge noncutting needles over larger
needles for lumbar puncture to reduce the risk of PDPH (evidence grade: C; level of certainty:
moderate). Fourth, if using a cutting needle for lumbar puncture, insertion with the bevel parallel to
the long axis of the spine is preferred as it may reduce the risk of PDPH (evidence grade: B; level of
certainty: moderate).
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(evidence grade: C; level of certainty: low). Second, adequate hydration should be maintained with
oral fluids; intravenous fluid should be used when oral hydration cannot be maintained (evidence
grade: C; level of certainty: low). Third, evidence does not support the routine use of abdominal
binders or aromatherapy to treat PDPH (evidence grade: D; level of certainty: low).
Fourth, regular multimodal analgesia, including acetaminophen and nonsteroidal anti-
inflammatory drugs, should be offered to all patients with PDPH unless contraindicated41 (evidence
grade: B; level of certainty: low). Fifth, short-term use of opioids may be considered in the treatment
of PDPH if regular multimodal analgesia is ineffective (evidence grade C; level of certainty: low);
long-term opioid use is not recommended in the treatment of PDPH (evidence grade: D; level of
certainty: moderate).
Sixth, caffeine may be offered in the first 24 hours of symptoms with a maximum dose of 900
mg per day (200-300 mg if breastfeeding) and avoiding multiple sources to prevent adverse effects
(evidence grade: B; level of certainty: low). Seventh, evidence does not support the routine use of
hydrocortisone, theophylline, triptans, adrenocorticotropic hormone or cosyntropin, neostigmine or
atropine, piritramide, methergine, and gabapentin in the management of PDPH (evidence grade: I;
level of certainty: low). Important supporting references were Russell et al7 and Basurto Ona et al.42
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Eleventh, informed consent for an EBP should include the potential for repeat dural puncture,
backache, and neurological complications (evidence grade: A; level of certainty: high). Twelfth, to
minimize complications, blood should be injected slowly and incrementally. If the patient develops
substantial backache or headache (eg, pressure paresthesia), injection of blood should be stopped
and resumed based on clinical judgment when symptoms resolve (evidence grade: B; level of
certainty: moderate). Thirteenth, after an EBP, if backache persists, increases in severity, or changes
in nature, other diagnoses should be investigated (evidence grade: C; level of certainty: low).
Fourteenth, epidural analgesia and anesthesia can be effective in patients with a history of EBP and
should not be withheld (evidence grade: C; level of certainty: low). Important supporting references
were Russell et al8 and Boonmak and Boonmak.40
Question 10: What Are the Long-Term Complications of PDPH, and How Should Patients Be
Followed Up?
Statements for this question were as follows. First, evidence showed an association between
inadvertent dural puncture and/or PDPH with chronic headache, backache, neckache, depression,
cranial nerve palsy, SDH, or CVST (level of certainty: moderate). Second, evidence was insufficient to
determine whether EBP mitigates, prevents, or treats these sequelae (level of certainty: low). Third,
PDPH was associated with the development of chronic headache (level of certainty: moderate).
There were 5 recommendations for this question. First, before discharge, information regarding
PDPH sequelae should be conveyed to patients, with arrangements for appropriate follow-up and
contact information of their anesthesiologist and other health care practitioners (evidence grade: B;
level of certainty: moderate). Second, the clinician (or team member) responsible for dural puncture
leading to PDPH should ensure that other specialties or primary care physicians are informed of
PDPH management and the potential for long-term symptoms (evidence grade: B; level of certainty:
moderate).
Third, follow-up with patients who experience PDPH should be continued until headache
resolves (evidence grade: B; level of certainty: moderate). Fourth, after discharge from the hospital,
follow-up may be continued by the primary care physician. Information regarding PDPH diagnosis
and/or inadvertent dural puncture should be communicated to the primary care physician and other
specialists, with referrals to a pain or neurology specialist if indicated (evidence grade: C; level of
certainty: low). Fifth, urgent neuroimaging and referral to an appropriate specialist should be
performed for any patient with PDPH who has worsening symptoms despite an EBP, new focal
neurologic symptoms, or a change in the nature of headache (evidence grade: B; level of certainty:
moderate). Important supporting references were Mims et al51 and Barad et al.52
Discussion
The current practice guidelines we developed provide structured and evidence-based
recommendations on pertinent aspects of PDPH, including risk factors, diagnosis, preventive and
prophylactic measures, and therapeutic options and their adverse effects. These systematic and
evidence-based practice guidelines for PDPH diagnosis and management may reduce morbidity and
mortality in patients with PDPH. In addition, they may reduce the economic implications for the
health care system and society. The diagnostic criteria for PDPH have changed with subsequent
iterations of the IHS guidelines,16 and while the understanding of the pathophysiological processes
and clinical course of PDPH continues to evolve, diagnostic criteria may again change over time.
A crucial aspect of these practice guidelines is identifying risk factors before performing an
intentional dural puncture or a procedure that carries the potential risk of unintentional dural
puncture to mitigate the risks. The clinician should assess the procedure’s risk-benefit profile and
consider whether dural puncture is justifiable. Salient risk factors delineated in these practice
guidelines that showed a high level of certainty, such as needle size, type of needle, and patient
factors (younger age and female sex), need to be considered before offering neuraxial procedures.
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Another vital aspect of these practice guidelines is incorporating an informed consent process
for the possibility of PDPH before performing neuraxial procedures. Any center offering lumbar
puncture or neuraxial procedures should have a policy on postdischarge follow-up of patients. The
policy should include (1) inpatient and outpatient services for identifying and managing PDPH, (2) a
plan to diagnose and manage PDPH until resolution, and (3) a pathway to access care to identify and
prevent complications of PDPH. Because symptoms of PDPH are similar to other causes of headache,
including those associated with intracranial hypertension (such as SDH and CVST), a high index of
suspicion should exist when typical features of PDPH are not present or when therapies for PDPH
remain ineffective.
Limitations
There were multiple challenges to developing evidence-based practice guidelines for PDPH,
including the wide variety of practice conditions and heterogeneity of the patient population. The
evidence review we conducted focused on adult patients, with most of the evidence emanating from
publications on anesthesia and lacks patient representation. The review may not have encompassed
all clinical scenarios (eg, diagnostic dural punctures, intrathecal chemotherapy, and chronic pain
interventions) or special populations (eg, pediatric population or patients with multiple
comorbidities). Future studies on the effectiveness of diagnostic and therapeutic options and the
prevention of serious complications of PDPH are needed. Investigators may consider novel study
methods, such as registry trials and adaptive study designs, as conventional study methods (eg,
randomized clinical trials) may be impractical due to low event rates.
Despite advances in evaluation and management of PDPH in the past decades, several
recommendations remained of moderate to low certainty because of the source studies’ small
sample size, suboptimal design, or, at times, out-of-date evidence. A prime example was the frequent
use of caffeine in the management of PDPH, which was based on limited evidence from 2 small
randomized clinical trials.53,54 However, excessive caffeine administration may be associated with
adverse effects, such as withdrawal, dehydration, and even seizures. Similarly, 4 randomized clinical
trials55-58 investigated ideal timing for EBP. Their results were conflicting, but overall, there is
opportunity for additional trials to improve the evidence on this topic. In obstetric settings, most
observational studies suggested that EBP failure (defined as requiring more than 1 EBP) was more
likely when EBP was performed within 24 to 48 hours of dural puncture.8 Data from observational
studies may have selection bias. In patients with severe headaches within 24 hours of the puncture,
the dural hole may be large enough to cause a severe CSF leak that requires further intervention (ie,
repeat EBP).
Another reason for the moderate to low certainty of evidence was emerging therapies, notably
the procedural options for PDPH management. Several interventional techniques, such as greater
occipital nerve block or sphenopalatine ganglion blocks, are novel therapies that need more robust
evidence. A similar scenario exists with optimal imaging guidance for performance of a blood patch
(fluoroscopic guidance vs landmark approach). Furthermore, with the availability of better evidence,
our confidence in the certainty of evidence for these recommendations may change.
Conclusions
This consensus statement found that current approaches to the treatment and management of
PDPH were not uniform and were hindered by the paucity of evidence. The practice guidelines we
developed provide a framework for individual clinicians to assess PDPH risk, confirm the diagnosis,
and adopt a systematic approach to its management.
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ARTICLE INFORMATION
Accepted for Publication: June 1, 2023.
Published: August 15, 2023. doi:10.1001/jamanetworkopen.2023.25387
Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2023 Uppal V
et al. JAMA Network Open.
Corresponding Author: Vishal Uppal, MBBS, MSc, Department of Anesthesia, Perioperative Medicine and Pain
Management, Dalhousie University, 1276 South Park St, 10W Victoria, Halifax, NS B3H 2Y9, Canada
(v.uppal@dal.ca).
Author Affiliations: Department of Anesthesia, Perioperative Medicine and Pain Management, Dalhousie
University, Halifax, Nova Scotia, Canada (Uppal); Nuffield Department of Anaesthetics, Oxford University Hospitals
National Health Service (NHS) Foundation Trust, Oxford, England (Russell); Department of Anesthesia, University
of Iowa Carver College of Medicine, Iowa City (Sondekoppam); Anesthesia Department, Stanford Health Care,
Stanford, California (Ansari); Department of Anesthesiology and Perioperative Medicine, Newton-Wellesley
Hospital, Tufts University School of Medicine, Boston, Massachusetts (Baber); Department of Anesthesiology,
Perioperative and Pain Medicine, Stanford University, Stanford, California (Chen); Department of Anesthesiology,
Critical Care and Pain Management, Hospital for Special Surgery, New York, New York (DelPizzo); Department of
Anaesthesia and Intensive Care, Emergency County Hospital, Cluj-Napoca, Romania (Dîrzu); Department of
Anesthesiology and Perioperative Medicine, Mayo Clinic, Jacksonville, Florida (Kalagara); Department of
Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, Minnesota (Kissoon); Department of
Radiology, Duke University Medical Center, Durham, North Carolina (Kranz); Yale University School of Medicine,
Yale New Haven Hospital and Bridgeport Hospital, New Haven, Connecticut (Leffert); Department of
Anesthesiology and Perioperative Medicine, Department of Obstetrics and Gynecology, University of Pittsburgh
School of Medicine, University of Pittsburgh Medical Center Magee Hospital, Pittsburgh, Pennsylvania (Lim);
Anesthesiology Institute, Interventional Pain Medicine Department, Cleveland Clinic Abu Dhabi, Abu Dhabi, United
Arab Emirates (Lobo); Department of Anaesthesia, London Northwest University Healthcare NHS Trust, London,
England (Lucas); Anaesthesiology Department, Creta Interclinic Hospital–Hellenic Healthcare Group, Heraklion,
Crete, Greece (Moka); Walter Reed National Military Medical Center, Bethesda, Maryland (Rodriguez); Department
of Anesthesia, University of Western Ontario, London, Ontario, Canada (Sehmbi); Medical Education,
Anesthesiology, Obstetrics and Gynecology, West Virginia University, Morgantown (Vallejo); Department of
Anaesthesiology, Intensive Care and Pain Therapy, Saarland University Medical Center and Saarland University
Faculty of Medicine, Saarbrücken, Germany (Volk); Rootstown and Center for Pain Medicine, Western Reserve
Hospital, Cuyahoga Falls, Ohio (Narouze).
Author Contributions: Drs Uppal and Russell had full access to all of the data in the study and take responsibility
for the integrity of the data and the accuracy of the data analysis.
Concept and design: Uppal, Sondekoppam, Ansari, Baber, Chen, Dîrzu, Kalagara, Kissoon, Leffert, Lim, Lucas,
Moka, Sehmbi, Vallejo, Volk, Narouze.
Acquisition, analysis, or interpretation of data: Uppal, Russell, Sondekoppam, Ansari, Baber, Chen, DelPizzo, Dîrzu,
Kissoon, Kranz, Leffert, Lim, Lobo, Lucas, Moka, Rodriguez, Sehmbi, Vallejo, Volk, Narouze.
Drafting of the manuscript: Uppal, Russell, Baber, Chen, DelPizzo, Dîrzu, Kalagara, Kissoon, Kranz, Leffert, Lim,
Lobo, Lucas, Moka, Rodriguez, Sehmbi, Vallejo, Volk, Narouze.
Critical review of the manuscript for important intellectual content: Uppal, Russell, Sondekoppam, Ansari, Baber,
Chen, DelPizzo, Dîrzu, Kalagara, Kissoon, Kranz, Leffert, Lim, Lobo, Lucas, Rodriguez, Vallejo, Volk, Narouze.
Administrative, technical, or material support: Uppal, Sondekoppam, Baber, Chen, Dîrzu, Kissoon, Leffert, Lim,
Lobo, Lucas, Sehmbi, Vallejo, Narouze.
Supervision: Narouze.
Conflict of Interest Disclosures: Dr Uppal reported being the associate editor of the Canadian Journal of
Anesthesia. Dr Sondekoppam reported receiving personal fees from CIVCO Medical Instruments Co outside the
submitted work. Dr Kissoon reported receiving grants from Nevro, royalties from UpToDate, and consulting fees
from Bright Minds Biosciences outside the submitted work. Dr Lim reported receiving salary support from the
National Institutes of Health Office of Research on Women’s Health, consulting fees from Octapharma, Heron
Pharmaceuticals, and for medical expert testimony; grants from Edwards Lifesciences, and royalties from
Cambridge University Press outside the submitted work. Dr Volk reported receiving lecture fees from B. Braun
Medical and Pajunk outside the submitted work. No other disclosures were reported.
Additional Contributions: Angela Stengel, MS, CAE, American Society of Regional Anesthesia and Pain Medicine,
provided project coordination, and Kristy Hancock, MLIS, Maritime Strategy for Patient-Oriented Research
Support for People and Patient-Oriented Research and Trials Unit Research Services, assisted with the literature
search. These individuals received no additional compensation, outside of their usual salary, for their
JAMA Network Open. 2023;6(8):e2325387. doi:10.1001/jamanetworkopen.2023.25387 (Reprinted) August 15, 2023 11/14
contributions. The Department of Anesthesia at the Perioperative Medicine and Pain Management of Dalhousie
University provided the open access fee for this publication. Editorial assistance from Nascent Medical LLC was
funded by ASRA Pain Medicine.
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SUPPLEMENT.
eAppendix 1. Search Summary
eAppendix 2. Full Reference List Supporting the Recommendations and Statements
eAppendix 3. The Final Level of Agreement for Each Recommendation
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