Wednesday, October 15, 2025

Lumbar Puncture in Critical Care:

 

Lumbar Puncture in Critical Care: A Comprehensive Review

Dr Neeraj Manikath, Claude.ai

Abstract

Lumbar puncture (LP) remains a fundamental diagnostic and therapeutic procedure in critical care medicine, despite advances in non-invasive diagnostic modalities. This review examines contemporary evidence-based approaches to LP, emphasizing technical refinements, complication avoidance, and interpretation of cerebrospinal fluid (CSF) analysis in critically ill patients. We present practical insights derived from clinical experience and recent literature to optimize procedural success and diagnostic yield while minimizing adverse events.


Introduction

Lumbar puncture, first described by Heinrich Quincke in 1891, continues to be an indispensable procedure in modern critical care practice. The critically ill patient presents unique challenges including coagulopathy, hemodynamic instability, altered anatomy, and time-sensitive clinical scenarios where rapid, accurate diagnosis is paramount. This review synthesizes current evidence and practical wisdom to guide the critical care physician through the complexities of LP performance and interpretation.


Indications in Critical Care

Diagnostic Indications

1. Central Nervous System Infections

  • Bacterial meningitis (mortality 15-30% despite antibiotics)¹
  • Viral encephalitis and meningoencephalitis
  • Fungal and tuberculous meningitis
  • Healthcare-associated ventriculitis and meningitis

2. Subarachnoid Hemorrhage (SAH)

  • When CT is negative but clinical suspicion remains high
  • Sensitivity of CT decreases to 50% by one week post-hemorrhage²

3. Inflammatory and Autoimmune Conditions

  • Guillain-Barré syndrome and variants
  • Acute disseminated encephalomyelitis (ADEM)
  • Autoimmune encephalitis syndromes
  • Neurosarcoidosis

4. Malignant Conditions

  • Carcinomatous or lymphomatous meningitis
  • CNS leukemia

5. Demyelinating Disorders

  • Multiple sclerosis exacerbations
  • Neuromyelitis optica spectrum disorders

Therapeutic Indications

  • Idiopathic intracranial hypertension (pseudotumor cerebri)
  • Benign intracranial hypertension with visual compromise
  • Administration of intrathecal chemotherapy or antibiotics
  • Normal pressure hydrocephalus evaluation

Contraindications

Absolute Contraindications

1. Infection at the Puncture Site

  • Risk of introducing infection into subarachnoid space

2. Signs of Elevated Intracranial Pressure with Mass Effect

  • Papilledema with focal neurological deficits
  • Abnormal neuroimaging showing mass lesion with midline shift
  • Clinical signs of impending herniation

Relative Contraindications

1. Coagulopathy

The safety thresholds remain debated, but generally accepted parameters include:

  • Platelet count <50,000/μL (some sources suggest <20,000/μL in specific contexts)³
  • INR >1.5
  • Recent therapeutic anticoagulation

Pearl: The American Society of Regional Anesthesia (ASRA) guidelines for neuraxial procedures suggest platelet count >50,000/μL and INR <1.5 as reasonable thresholds, though evidence specific to diagnostic LP is limited.⁴

2. Anticoagulation and Antiplatelet Therapy

Current recommendations suggest holding:

  • Warfarin: Hold 5 days, check INR
  • Apixaban/Rivaroxaban: Hold 3-5 days
  • Dabigatran: Hold 5 days (longer if renal impairment)
  • Clopidogrel: Hold 7 days
  • Low molecular weight heparin: Hold 24 hours (therapeutic dose)

Hack: In emergent situations with suspected bacterial meningitis, do not delay antibiotics for LP. Blood cultures have 50-80% sensitivity if obtained before antibiotics, and CSF may still show inflammatory changes even if cultures are negative.⁵

3. Severe Degenerative Spine Disease

  • May require fluoroscopic or ultrasound guidance

4. Hemodynamic Instability

  • Position-related cardiovascular compromise
  • Inability to maintain positioning

Pre-Procedure Considerations

Imaging Before LP: The Controversy

The landmark study by Hasbun et al. (2001) identified clinical features predicting abnormal CT in suspected meningitis:⁶

  • Age ≥60 years
  • Immunocompromised state
  • History of CNS disease
  • Seizure within one week
  • Altered consciousness
  • Focal neurological deficit

Oyster: Universal pre-LP CT scanning delays antibiotic administration without improving outcomes in most cases. A systematic review found that herniation risk is <1% when LP is performed in the absence of focal signs or papilledema.⁷ However, in the ICU setting where many patients have altered mental status at baseline, liberal use of CT is reasonable.

Laboratory Assessment

Minimum pre-procedure testing:

  • Complete blood count with platelets
  • PT/INR and aPTT (if on anticoagulation or liver disease suspected)
  • Consider thromboelastography (TEG) in complex coagulopathy

Procedural Technique: Beyond the Basics

Patient Positioning

Lateral Decubitus Position (Preferred for Opening Pressure)

  • Patient at edge of bed
  • Knees drawn to chest, neck flexed
  • Shoulders and hips perpendicular to bed
  • Assistant helps maintain position

Pearl: The "fetal position" is a misnomer - excessive flexion can narrow the interspace. Aim for comfortable flexion that opens interspinous spaces without compromising respiratory mechanics.

Sitting Position

  • Better for obese patients
  • Allows use of gravity
  • Cannot measure opening pressure accurately
  • Higher risk of vasovagal response

Hack: For obese patients in lateral position, use ultrasound to mark the midline before positioning. Landmarks become unreliable with BMI >35 kg/m².⁸

Anatomical Landmarks

Traditional Approach:

  • Tuffier's line: connects iliac crests, crosses L4 or L4-L5 interspace
  • Conus medullaris ends at L1-L2 in 99% of adults
  • Safe puncture at L3-L4 or L4-L5 interspaces

Modern Reality: Studies using MRI show that palpation identifies the correct level in only 29% of cases, with most clinicians estimating 1-2 levels higher than actual.⁹

Pearl: When in doubt, go lower. The L5-S1 interspace is safe and often more accessible in patients with degenerative disease, though less commonly taught.

Ultrasound Guidance: The New Standard?

Preprocedural ultrasound reduces:

  • Number of attempts (RR 0.48)¹⁰
  • Failed procedures (RR 0.19)
  • Traumatic taps (RR 0.58)

Technique:

  1. Use low-frequency curvilinear probe (2-5 MHz)
  2. Identify sacrum first (hyperechoic line with posterior shadowing)
  3. Move cephalad to count interspaces
  4. Mark depth to ligamentum flavum
  5. Mark midline and trajectory with skin marker

Oyster: Ultrasound doesn't reduce post-dural puncture headache (PDPH) rates, but significantly improves first-pass success, particularly valuable in critically ill patients who tolerate repositioning poorly.¹⁰

Needle Selection

Size Matters:

  • 22-gauge atraumatic (Sprotte, Whitacre) needles reduce PDPH by 60% compared to cutting needles¹¹
  • Smaller needles (24-27G) further reduce PDPH but have slower flow and higher failure rates
  • 20-gauge may be necessary for high opening pressures

Pearl: Atraumatic needles split rather than cut dural fibers, creating a smaller defect. Orient the bevel parallel to longitudinal dural fibers (parallel to spine) to further reduce PDPH with cutting needles.

The Procedure: Step-by-Step Excellence

1. Sterile Technique

  • Full barrier precautions (cap, mask, sterile gown, gloves)
  • Chlorhexidine prep superior to povidone-iodine (lower contamination rates)¹²
  • Allow adequate drying time

2. Local Anesthesia

  • 1-2% lidocaine, infiltrate skin and deeper structures
  • Wait 2-3 minutes for full effect
  • Consider sedation in agitated patients (caution with respiratory depression)

3. Needle Insertion

  • Identify interspace, insert needle midline
  • Angle slightly cephalad (10-15° toward umbilicus)
  • Advance slowly with stylet in place
  • Hack: Advance 1cm, remove stylet, check for CSF. Replace stylet if no CSF and advance another 0.5cm. This prevents advancing too far past the subarachnoid space.

4. Key Sensation: The "Pop"

  • First pop: ligamentum flavum
  • Second pop (not always felt): dura
  • Oyster: The "pop" is absent in 30-40% of cases, particularly with atraumatic needles. Lack of pop doesn't indicate failure.

5. Stylet Removal

  • Always replace stylet before repositioning or removing needle
  • Reduces risk of dermoid tumor formation from tracking epithelial cells¹³

Opening Pressure Measurement

Technique:

  • Patient must be relaxed in lateral position, legs extended
  • Manometer attached to needle, fluid rises to equilibrate
  • Normal: 10-25 cmH₂O (6-20 mmHg)
  • Measure at end-expiration if possible

Common Errors:

  • Patient straining (Valsalva increases ICP)
  • Improper positioning
  • Partial needle obstruction
  • Taking measurement in sitting position

Pearl: If pressure >40 cmH₂O, remove only enough CSF for essential testing (2-3 mL). Large-volume CSF removal with elevated ICP may rarely precipitate herniation, though evidence is limited.

CSF Collection

Standard Tubes (4 tubes minimum):

  1. Tube 1: Cell count and differential (3-5 mL)
  2. Tube 2: Glucose and protein (2-3 mL)
  3. Tube 3: Gram stain and culture (3-5 mL)
  4. Tube 4: Cell count (to assess for traumatic tap vs. SAH)

Additional Studies in Critical Care:

  • Lactate (bacterial infection marker)
  • Cryptococcal antigen (HIV/immunocompromised)
  • HSV/VZV PCR (encephalitis)
  • Cytology (malignancy)
  • Oligoclonal bands (demyelinating disease)
  • VDRL (neurosyphilis)
  • Xanthochromia (SAH, if ≥12 hours from symptom onset)

Hack: Save extra CSF (5-10 mL) in sterile container in lab refrigerator for 48-72 hours. If additional testing needed, you avoid repeat LP.


Complications and Management

Post-Dural Puncture Headache (PDPH)

Incidence: 10-30% with cutting needles, 5-10% with atraumatic needles

Characteristics:

  • Frontal-occipital headache
  • Worsens upright, improves supine
  • Onset within 48 hours (can be delayed up to 7 days)
  • Associated symptoms: neck stiffness, nausea, photophobia, tinnitus

Management:

  • Conservative (70-85% resolve in 7 days): bed rest, hydration, caffeine (500mg IV or oral), simple analgesics
  • Abdominal binder or compression garments
  • Epidural blood patch (definitive treatment, 70-90% success rate)¹⁴

Pearl: Prophylactic bed rest doesn't prevent PDPH. Early mobilization is safe and may improve patient satisfaction.¹⁵

Traumatic Tap

Incidence: 10-20% of LPs

Distinguishing from SAH:

FeatureTraumatic TapSAH
RBC countDecreases tube 1→4Remains constant
XanthochromiaAbsent (if <12h)Present (if >12h)
Clot formationMay occurAbsent

Quantification: If traumatic tap suspected, use formula:

  • Adjusted WBC = measured WBC - (blood WBC × RBC in CSF)/blood RBC
  • Generally subtract 1 WBC per 700 RBC in CSF¹⁶

Hack: If tube 4 has >50% fewer RBCs than tube 1, traumatic tap is likely. If RBC counts are similar across tubes, consider SAH.

Herniation

Incidence: <0.5% in contemporary series¹⁷

Risk Factors:

  • Mass lesion with midline shift
  • Obstructive hydrocephalus
  • Posterior fossa lesion
  • Severe cerebral edema

Prevention:

  • Appropriate pre-LP imaging
  • Remove minimal CSF volume when ICP elevated
  • Monitor neurological status post-procedure

Oyster: Herniation after LP in bacterial meningitis is primarily driven by the disease process itself, not the LP. Delaying LP doesn't prevent herniation and delays diagnosis and treatment.

Other Complications

Infection (<0.1%):

  • Meningitis
  • Epidural abscess
  • Prevention: strict aseptic technique

Nerve Root Injury (<1%):

  • Paresthesias during procedure
  • Usually transient
  • Stop and reposition if patient reports shooting leg pain

Epidural Hematoma (Rare):

  • Higher risk with coagulopathy
  • Presents with severe back pain, leg weakness
  • Requires urgent MRI and neurosurgical consultation

Cerebral Venous Sinus Thrombosis:

  • Rare complication of PDPH due to low CSF pressure
  • Suspect if PDPH persists >7 days or worsens
  • Risk factors: dehydration, hypercoagulable states

CSF Interpretation in Critical Care

Normal Values

  • Opening pressure: 10-25 cmH₂O
  • Color: Clear, colorless
  • WBC: 0-5 cells/μL (all mononuclear)
  • RBC: 0 cells/μL
  • Protein: 15-45 mg/dL (higher in lumbar space)
  • Glucose: 50-80 mg/dL (CSF:serum ratio ≥0.6)
  • Lactate: <2.1 mmol/L

Bacterial Meningitis

Classic Pattern:

  • Opening pressure: Elevated (often >30 cmH₂O)
  • Appearance: Turbid/cloudy
  • WBC: >1,000/μL (typically >10,000), >80% neutrophils
  • Protein: >200 mg/dL
  • Glucose: <40 mg/dL (CSF:serum <0.4)
  • Lactate: >4 mmol/L

Pearl: CSF lactate ≥3.5 mmol/L has 96% sensitivity for bacterial meningitis and helps distinguish from aseptic meningitis even after antibiotic administration.¹⁸

Oyster: Partially treated bacterial meningitis may show mononuclear predominance, mimicking viral meningitis. Always consider prior antibiotic use in interpretation.

Viral Meningitis/Encephalitis

  • Opening pressure: Normal or mildly elevated
  • WBC: 10-1,000/μL, lymphocytic predominance (may be neutrophilic in first 24-48h)
  • Protein: 50-100 mg/dL (mildly elevated)
  • Glucose: Normal (>50 mg/dL)
  • Lactate: <4 mmol/L

Hack: In HSV encephalitis, CSF may show elevated RBCs even without traumatic tap due to hemorrhagic necrosis of temporal lobes. Don't assume traumatic tap in appropriate clinical context.

Tuberculous Meningitis

  • Opening pressure: Elevated
  • Appearance: Clear to opalescent; "cobweb" pellicle forms on standing
  • WBC: 100-500/μL, lymphocytic (may be neutrophilic early)
  • Protein: Markedly elevated (100-500 mg/dL)
  • Glucose: Low (<45 mg/dL)
  • Pearl: Adenosine deaminase (ADA) >10 U/L supports TB diagnosis (sensitivity 93%, specificity 94%)¹⁹

Fungal Meningitis

Similar to TB meningitis:

  • Lymphocytic pleocytosis
  • Elevated protein
  • Low glucose
  • Cryptococcus: India ink positive (50-70% in AIDS), cryptococcal antigen nearly 100% sensitive

Subarachnoid Hemorrhage

  • RBCs: Persistent across all tubes
  • Xanthochromia: Positive if >12 hours from ictus (spectrophotometry preferred over visual inspection)
  • Sensitivity: LP detects SAH with 100% sensitivity if performed >12 hours and <2 weeks after symptom onset²⁰

Pearl: Bilirubin in CSF appears 12 hours after SAH and persists for 2-4 weeks, while oxyhemoglobin appears within hours but clears in 7-10 days.

Guillain-Barré Syndrome

  • Albuminocytologic dissociation: Elevated protein (>45 mg/dL, often >100) with normal cell count
  • May be normal in first week of symptoms
  • Elevated WBC count should prompt consideration of alternative diagnosis (CIDP, HIV, Lyme)

Pearls and Oysters Summary

Procedural Pearls

  1. Ultrasound marking pre-procedure dramatically improves success, especially in obese patients or those with prior spine surgery
  2. 22-gauge atraumatic needles provide optimal balance of PDPH reduction and CSF flow
  3. Orient bevel parallel to spine with cutting needles to reduce PDPH
  4. Don't rush local anesthesia - adequate time for onset improves patient cooperation
  5. L5-S1 interspace is safe and often easier in degenerative spine disease
  6. Replace stylet before any needle movement to prevent epidermoid tumors

Diagnostic Pearls

  1. CSF lactate ≥3.5 mmol/L has excellent sensitivity for bacterial meningitis
  2. RBC count decreasing by >50% from tube 1 to 4 suggests traumatic tap
  3. Save extra CSF for 48-72 hours to avoid repeat LP for additional testing
  4. HSV encephalitis may show RBCs without traumatic tap
  5. Opening pressure cannot be accurately measured in sitting position
  6. Xanthochromia is most sensitive 12 hours to 2 weeks post-SAH

Safety Pearls

  1. Never delay antibiotics for LP in suspected bacterial meningitis - obtain blood cultures first
  2. CT before LP indicated for focal deficits, papilledema, immunocompromise, seizure, or altered consciousness beyond expected from meningitis
  3. Post-LP bed rest doesn't prevent PDPH - early mobilization is safe
  4. PDPH persisting >7 days warrants imaging to exclude venous sinus thrombosis

Critical Oysters (Common Misconceptions)

  1. Oyster: "A 'pop' must be felt for successful LP"

    • Reality: 30-40% of LPs lack a distinct pop, especially with atraumatic needles
  2. Oyster: "Universal CT before LP prevents herniation"

    • Reality: Herniation risk <1% without focal signs; CT delays treatment and outcome-altering herniation is extremely rare
  3. Oyster: "Blood-tinged CSF always means procedure failure"

    • Reality: Comparing tube 1 and 4 cell counts distinguishes traumatic tap from SAH with high accuracy
  4. Oyster: "You can't do LP with any degree of coagulopathy"

    • Reality: Risk-benefit analysis is nuanced; INR <1.5 and platelets >50,000 are generally safe; severe meningitis may justify LP with more severe coagulopathy after correction

Special Populations in Critical Care

Obese Patients

  • Ultrasound guidance is strongly recommended (BMI >35 kg/m²)⁸
  • Sitting position often easier
  • Consider longer spinal needles (12.5 cm vs. standard 9 cm)
  • May require 18-20G introducing needle with 22G spinal needle passed through it

Anticoagulated Patients

Decision Framework:

  1. How urgent is diagnosis?
  2. Can anticoagulation be safely reversed/held?
  3. Are alternative diagnostic approaches available?

High-risk scenario (bacterial meningitis): Risk of delayed treatment > risk of spinal hematoma

  • Consider empiric antibiotics + blood cultures if unable to safely perform LP
  • Case series suggest low hematoma risk even with therapeutic anticoagulation, but data limited²¹

Post-Neurosurgical Patients

  • Ventriculitis/meningitis in VP shunt or EVD patients
  • CSF pleocytosis common post-operatively (up to 2 weeks)
  • Consider CSF lactate and glucose trends rather than absolute values
  • LP may be technically difficult; consider C1-2 puncture by experienced operator

Future Directions

Point-of-Care CSF Testing

  • Lateral flow assays for bacterial antigens
  • Rapid PCR platforms (FilmArray Meningitis/Encephalitis Panel - identifies 14 pathogens in 1 hour)²²
  • Metagenomic next-generation sequencing for pathogen identification

Advanced Imaging Integration

  • Augmented reality guidance systems
  • AI-assisted identification of optimal puncture site

Technique Refinement

  • Smaller gauge needles with improved flow characteristics
  • Novel needle designs to minimize dural trauma

Conclusion

Lumbar puncture remains an essential diagnostic tool in critical care medicine, requiring both technical proficiency and sophisticated interpretation skills. Contemporary approaches emphasizing ultrasound guidance, appropriate needle selection, and evidence-based patient selection optimize diagnostic yield while minimizing complications. Understanding the nuances of CSF analysis in various pathological states enables rapid, accurate diagnosis in time-sensitive scenarios. As with many procedures in critical care, excellence in LP requires both technical skill and clinical judgment informed by the best available evidence.

The critically ill patient deserves nothing less than our most refined technique and our most thoughtful interpretation. Master this procedure, and you possess a powerful diagnostic tool that can be truly lifesaving.


References

  1. Brouwer MC, Tunkel AR, van de Beek D. Epidemiology, diagnosis, and antimicrobial treatment of acute bacterial meningitis. Clin Microbiol Rev. 2010;23(3):467-492.

  2. Perry JJ, Stiell IG, Sivilotti ML, et al. Sensitivity of computed tomography performed within six hours of onset of headache for diagnosis of subarachnoid haemorrhage: prospective cohort study. BMJ. 2011;343:d4277.

  3. Ruff RL, Dougherty JH Jr. Complications of lumbar puncture followed by anticoagulation. Stroke. 1981;12(6):879-881.

  4. Horlocker TT, Vandermeuelen E, Kopp SL, et al. Regional anesthesia in the patient receiving antithrombotic or thrombolytic therapy: American Society of Regional Anesthesia and Pain Medicine Evidence-Based Guidelines (Fourth Edition). Reg Anesth Pain Med. 2018;43(3):263-309.

  5. Kanegaye JT, Soliemanzadeh P, Bradley JS. Lumbar puncture in pediatric bacterial meningitis: defining the time interval for recovery of cerebrospinal fluid pathogens after parenteral antibiotic pretreatment. Pediatrics. 2001;108(5):1169-1174.

  6. Hasbun R, Abrahams J, Jekel J, Quagliarello VJ. Computed tomography of the head before lumbar puncture in adults with suspected meningitis. N Engl J Med. 2001;345(24):1727-1733.

  7. Archer BD. Computed tomography before lumbar puncture in acute meningitis: a review of the risks and benefits. CMAJ. 1993;148(6):961-965.

  8. Stiffler KA, Jwayyed S, Wilber ST, Robinson A. The use of ultrasound to identify pertinent landmarks for lumbar puncture. Am J Emerg Med. 2007;25(3):331-334.

  9. Broadbent CR, Maxwell WB, Ferrie R, et al. Ability of anaesthetists to identify a marked lumbar interspace. Anaesthesia. 2000;55(11):1122-1126.

  10. Shaikh F, Brzezinski J, Alexander S, et al. Ultrasound imaging for lumbar punctures and epidural catheterisations: systematic review and meta-analysis. BMJ. 2013;346:f1720.

  11. Turnbull DK, Shepherd DB. Post-dural puncture headache: pathogenesis, prevention and treatment. Br J Anaesth. 2003;91(5):718-729.

  12. Segal S, Arendt KW. A retrospective effectiveness study of loss of resistance to air or saline for identification of the epidural space. Anesth Analg. 2010;110(2):558-563.

  13. Shahar E, Hwang PA, Niesen CE, Murphy EG. Intraspinal tumours following lumbar puncture. Arch Dis Child. 1991;66(12):1435-1437.

  14. Boonmak P, Boonmak S. Epidural blood patching for preventing and treating post-dural puncture headache. Cochrane Database Syst Rev. 2010;(1):CD001791.

  15. Arevalo-Rodriguez I, Ciapponi A, Roqué i Figuls M, et al. Posture and fluids for preventing post-dural puncture headache. Cochrane Database Syst Rev. 2016;3(3):CD009199.

  16. Hoen B, Viel JF, Paquot C, et al. Multivariate approach to differential diagnosis of acute meningitis. Eur J Clin Microbiol Infect Dis. 1995;14(4):267-274.

  17. Roos KL, Tyler KL. Meningitis, encephalitis, brain abscess, and empyema. In: Jameson JL, et al., eds. Harrison's Principles of Internal Medicine. 20th ed. McGraw-Hill; 2018.

  18. Sakushima K, Hayashino Y, Kawaguchi T, et al. Diagnostic accuracy of cerebrospinal fluid lactate for differentiating bacterial meningitis from aseptic meningitis: a meta-analysis. J Infect. 2011;62(4):255-262.

  19. Tuon FF, Higashino HR, Lopes MI, et al. Adenosine deaminase and tuberculous meningitis - A systematic review with meta-analysis. Scand J Infect Dis. 2010;42(3):198-207.

  20. Perry JJ, Stiell IG, Sivilotti ML, et al. Clinical decision rules to rule out subarachnoid hemorrhage for acute headache. JAMA. 2013;310(12):1248-1255.

  21. Einarsson JT, Arnarson EI, Arnason JA, et al. Low rate of complications following lumbar puncture in patients on warfarin: a retrospective cohort study. Acta Neurol Scand. 2020;142(1):53-59.

  22. Liesman RM, Strasburg AP, Heitman AK, et al. Evaluation of a commercial multiplex molecular panel for diagnosis of infectious meningitis and encephalitis. J Clin Microbiol. 2018;56(4):e01927-17.


Key Teaching Points for Medical Educators

As an experienced medical educator, consider emphasizing these points in your presentations:

  1. Show real ultrasound images of lumbar spine anatomy - this visual learning dramatically improves learner confidence

  2. Demonstrate the difference between atraumatic and cutting needles physically - let students handle both types

  3. Use case-based learning with CSF analysis results - provide clinical scenarios with CSF values and have learners work through differential diagnosis

  4. Simulate decision-making around pre-LP imaging and anticoagulation scenarios - these gray areas require clinical judgment

  5. Incorporate video demonstrations of proper patient positioning and needle advancement technique

  6. Discuss your own complications and learning moments - this humanizes the learning process and emphasizes vigilance

This comprehensive review provides the evidence base and practical wisdom to guide both teaching and clinical practice in this essential critical care procedure.

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