Notes on local anasthesia under heading medicines,techniques, indication, contraindications, complication and management

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Local Anaesthesia - Comprehensive Notes


1. MEDICINES (Local Anaesthetic Drugs)

Local anaesthetics work by blocking neuronal sodium channels, thereby inhibiting depolarisation and preventing action potential formation across the nerve axon. Smaller unmyelinated C-fibres (pain, heat) are blocked more readily than larger myelinated A-delta fibres (pressure, motor), which explains why pain is abolished before pressure sensation at lower volumes.

Classification

Amide group (amino-amides):
DrugMax Dose (plain)Max Dose (+ adrenaline)OnsetDurationKey Notes
Lidocaine3 mg/kg (300 mg)7 mg/kg (500 mg)Rapid1-2 hoursMost widely used; infiltration and topical
Bupivacaine2 mg/kg (175 mg)2 mg/kg (250 mg)2-10 min3-10 hoursLong-acting; most cardiotoxic; NEVER use IV
Ropivacaine3-4 mg/kg-Moderate4-8 hoursLess cardiotoxic than bupivacaine; better sensory-motor separation
Levobupivacaine2 mg/kg-Moderate3-10 hoursS-isomer of bupivacaine; fewer cardiotoxic properties
Prilocaine6 mg/kg (400 mg)9 mg/kg (600 mg)Rapid2-4 hoursLeast systemic toxicity; causes methaemoglobinaemia
Mepivacaine300 mg400 mg3-20 min2-3 hoursInfiltration
Ester group (amino-esters):
DrugUseOnsetDurationNotes
Procaine (Novocain)InfiltrationSlow15-30 minMetabolised by plasma cholinesterase; allergic reactions more common
ChloroprocaineInfiltrationRapid0.5-2 hoursMax 600 mg
CocaineTopical only2-10 min1-3 hoursVasoconstrictor; used in nasal surgery
BenzocaineTopical onlyRapidShortUsed on mucous membranes
TetracaineSpinal / topicalModerateLongHigh potency

Special Preparations

  • EMLA (Eutectic Mixture of Local Anaesthetics) - lidocaine + prilocaine cream; applied to intact skin 60 minutes before venepuncture, especially in children
  • Moffett's solution - cocaine + adrenaline + sodium bicarbonate; used in nasal surgery for anaesthesia and vasoconstriction
  • Lidocaine 2/4/10% spray - used to anaesthetise the airway during awake fibreoptic intubation

Role of Adrenaline (Epinephrine) as Additive

Adding adrenaline to local anaesthetic solutions:
  • Hastens onset
  • Prolongs duration of action
  • Permits a higher upper dose limit (e.g., lidocaine rises from 3 mg/kg to 7 mg/kg)
  • Reduces systemic absorption and peak blood levels
  • Provides haemostasis in the operating field
Optimal concentration: 1:200,000 to 1:400,000
Buffering with sodium bicarbonate (NaHCO3): Mixing 8.4% NaHCO3 with 1% lidocaine in a 1:9 ratio reduces pain on injection by decreasing acidity. - Schwartz's Principles of Surgery, 11th ed.

2. TECHNIQUES

A. Topical Anaesthesia

Application of local anaesthetic directly to mucous membranes, skin, or wounds.
  • EMLA cream (skin for venepuncture)
  • Lidocaine spray (oropharynx, larynx for awake intubation)
  • Cocaine solution (nasal mucosa - provides anaesthesia + vasoconstriction)
  • Benzocaine/tetracaine gels (mucous membranes)

B. Local Infiltration

  • Direct injection into tissues around the operative site
  • Injection made in standard fan-shaped or ring fashion
  • Useful for simple lacerations, skin lesions, minor procedures
  • All local anaesthetics are less effective in areas of inflammation (lower pH reduces ionisation and drug activity)

C. Peripheral Nerve Blocks

Injection adjacent to a named nerve or nerve plexus to anaesthetise a defined anatomical region.
Upper limb:
  • Brachial plexus - interscalene approach: shoulder and proximal arm surgery; complications include phrenic nerve block (100%), Horner's syndrome, intravascular and spinal injection
  • Supraclavicular approach: excellent for entire upper limb; risk of pneumothorax
  • Infraclavicular approach: lower risk of pneumothorax; elbow and distal surgery
  • Axillary approach: forearm and hand; safest approach; low complication rate
  • Wrist blocks: radial, ulnar, and median nerve blocks at the wrist for hand surgery
  • Digital nerve blocks: metacarpal head level injection into flexor tendon sheath or dorsal web space; excellent for fingertip injuries
Lower limb:
  • Femoral nerve block: anaesthesia and analgesia for anterior thigh, knee (quadriceps surgery)
  • Sciatic nerve block: lower limb surgery; combined with femoral for complete leg anaesthesia
  • iPACK block (Infiltration between Popliteal Artery and Capsule of the Knee): targets genicular nerves under ultrasound guidance; minimises motor block
Trunk / Fascial plane blocks:
  • Transversus Abdominis Plane (TAP) block: local anaesthetic injected between internal oblique and transversus abdominis; blocks T6-L1 segmental nerves; effective for anterior abdominal wall analgesia after abdominal surgery
  • Quadratus lumborum (QL) block: targets abdominal nerves anterior to QL muscle; wider coverage than TAP
  • Erector spinae plane (ESP) block: blocks spinal nerves at various levels; used for thoracic and abdominal analgesia

D. Intravenous Regional Anaesthesia (Bier Block)

  • Lidocaine injected IV into an exsanguinated, tourniquet-occluded limb
  • Used for short upper limb procedures
  • Bupivacaine is absolutely contraindicated for this technique

E. Central Neuraxial Blocks

Spinal anaesthesia (subarachnoid block):
  • Local anaesthetic injected into the subarachnoid (intrathecal) space
  • Rapid onset, dense block
  • Common agents: bupivacaine (hyperbaric), lidocaine, tetracaine
Epidural anaesthesia:
  • Local anaesthetic injected into the epidural space
  • Slower onset, titratable, catheter allows continuous infusion
  • Used in obstetrics, major abdominal/thoracic/lower limb surgery, postoperative analgesia
  • Rescue lipid emulsion (20% Intralipid 1.5 mL/kg) must be available whenever epidural blocks are performed - Morgan & Mikhail's Clinical Anesthesiology, 7th ed.
Guidance technology: Nerve localisation has evolved from pure anatomical landmarks + paraesthesia (high risk of nerve damage and intravascular injection) to:
  • Nerve stimulator-guided blocks
  • Ultrasound-guided blocks (current standard - reduces vascular puncture and local anaesthetic toxicity, allows real-time visualisation of needle tip and drug spread)

3. INDICATIONS

Local anaesthesia is indicated when:
  1. Surgical procedures on skin, subcutaneous tissue, or superficial structures
  2. Minor surgical procedures: excision of skin lesions, wound repair, biopsy
  3. When general anaesthesia carries higher risk: debilitating respiratory or cardiovascular disease, morbid obesity, anticipated difficult airway
  4. Obstetric cases: epidural/spinal for labour analgesia, caesarean section
  5. Day-case surgery: avoids prolonged recovery from general anaesthesia
  6. Diagnostic and therapeutic procedures: lumbar puncture, joint injections, nerve blocks for pain management
  7. Postoperative pain management: as part of multimodal analgesia, reduces opioid requirements
  8. Awake procedures: fibreoptic intubation (lidocaine airway spray), awake craniotomy
  9. Patients who refuse general anaesthesia
  10. Regional anaesthesia as the sole technique for upper/lower limb surgery, hernia repair, perianal surgery

4. CONTRAINDICATIONS

Absolute Contraindications

  • Patient refusal of regional anaesthesia (absolute; adamant refusal by patient or guardian)
  • Allergy / known hypersensitivity to the specific local anaesthetic agent (ester class - true allergy is more common; amide allergy is rare but documented)
  • Injection into infected tissue or skin at the proposed site (risk of spreading infection, reduced drug efficacy due to low pH in inflamed tissue)
  • Bupivacaine IV (intravenous regional technique): absolutely contraindicated due to severe cardiotoxicity

Relative Contraindications

  • Systemic coagulopathy / anticoagulation therapy: risk of haematoma, especially with deep blocks and neuraxial techniques (follow ASRA guidelines)
  • Pre-existing neurological disease at the site of block: risk of compounding existing deficits; document baseline carefully and discuss risks
  • Cardiovascular disease (for adrenaline-containing solutions): hypertension, cardiac arrhythmia, coronary artery disease
  • Patients on monoamine oxidase inhibitors (MAOIs) or tricyclic antidepressants: avoid adrenaline-containing local anaesthetic solutions
  • End-arterial locations (for adrenaline): fingers, toes, penis, nose, earlobes, pinna - risk of ischaemia and gangrene
  • Contaminated wounds (for adrenaline): increased infection risk due to reduced blood flow
  • Thyrotoxicosis / diabetes / peripheral vascular disease: exaggerated vasoconstrictor response to adrenaline
  • Marginal skin flap viability: adrenaline risks flap ischaemia
  • Uncooperative or agitated patients: inability to maintain still for nerve block or wound exploration

5. COMPLICATIONS

Local Complications

ComplicationNotes
HaematomaInadvertent vascular puncture during block; most common with deep blocks (axillary, femoral, sciatic)
Infection / abscessBreach of sterility; can spread to deep spaces (e.g., hip joint, gluteal musculature, retrosoas space following pudendal block)
Nerve damage / neurotoxicityDirect needle trauma, intraneural injection, concentration-dependent toxicity; may cause paraesthesia, weakness, or chronic pain
Failure of blockIncomplete anaesthesia; most frequent complication with pudendal block
PneumothoraxWith supraclavicular brachial plexus block
Phrenic nerve palsyInterscalene approach (virtually 100%); significant in patients with contralateral phrenic palsy or poor respiratory reserve
Horner's syndromeInterscalene approach; stellate ganglion involvement

Systemic Complications (Local Anaesthetic Systemic Toxicity - LAST)

Mechanism: Accidental intravascular injection or excessive dose - sodium/potassium channel blockade throughout the body.
Absorption rate (highest to lowest): Intercostal > caudal > epidural > bupivacaine plexus > intravenous regional > lower extremity blocks
Neurological toxicity (early signs - may be masked under GA):
  • Tinnitus, metallic taste in mouth, perioral numbness
  • Malaise, light-headedness
  • Dysarthria, diplopia
  • Confusion, agitation
Neurological toxicity (late - progression):
  • Loss of consciousness
  • Generalised tonic-clonic seizures
Cardiovascular toxicity:
  • Palpitations, bradycardia or tachycardia
  • Conduction disorders: QRS widening, AV block
  • Torsades de pointes
  • Ventricular fibrillation
  • Cardiac arrest / asystole
Important: With bupivacaine, cardiac toxicity can occur simultaneously with or before neurological signs and is treatment-resistant. Bupivacaine-induced ventricular arrhythmias must NOT be treated with vasopressin, calcium channel blockers, beta-blockers, or other local anaesthetics (e.g., lidocaine as antiarrhythmic). - Miller's Anesthesia, 10th ed.
Prilocaine-specific: Methaemoglobinaemia from ortho-toluidine metabolite (causes cyanosis unresponsive to oxygen; treat with methylene blue 1-2 mg/kg IV)
Special risk in children: Neurological and cardiovascular signs occur simultaneously (not sequentially as in adults); rapid heart rate increases cardiac toxicity risk; plasma AGP (binding protein) is low at birth, increasing free drug fraction.

6. MANAGEMENT OF COMPLICATIONS

Management of LAST (Local Anaesthetic Systemic Toxicity)

Immediate steps (ABC approach):
  1. Stop injection immediately
  2. Call for help - this is a life-threatening emergency
  3. Airway: secure airway with 100% oxygen; early intubation prevents hypoxia and acidosis (both worsen cardiotoxicity)
  4. Venous access if not already established
  5. Monitoring: ECG, pulse oximetry, BP
Seizures:
  • Benzodiazepines (midazolam 0.05-0.1 mg/kg IV) are first-line for seizure control
  • Propofol may be used cautiously in small doses if haemodynamically stable (avoid in cardiovascular compromise)
  • Thiopentone to abort prolonged seizures
Cardiovascular collapse:
  • Begin CPR with standard chest compressions
  • Epinephrine: use titrated (small incremental) doses rather than large fixed boluses; 1-2 mcg/kg incremental boluses
  • Avoid: vasopressin, calcium channel blockers, beta-blockers, lidocaine (as antiarrhythmic)
  • For ventricular fibrillation: defibrillation (standard energy in adults; 2-4 J/kg in children)
Specific treatment - Lipid Rescue (Intralipid 20%):
  • Mechanism: "lipid sink" - Intralipid sequesters lipophilic local anaesthetic away from cardiac sodium channels; also improves cardiac energy metabolism; decreases cardiac bupivacaine concentration by ~11% within 3 minutes
  • Dose (adult): 20% Intralipid 1.5 mL/kg IV bolus, then infusion at 0.25 mL/kg/min for at least 10 minutes after cardiovascular stability is achieved; can repeat bolus up to 3 mL/kg total if no response
  • Dose (paediatric): 2-5 mL/kg IV bolus; may repeat up to 10 mL/kg
  • Should be available wherever major conduction blocks or large-volume infiltrations are performed
  • NOT a substitute for careful technique - it is an acute resuscitation tool only
  • Intralipid is most effective for bupivacaine toxicity
Methaemoglobinaemia (prilocaine):
  • Methylene blue 1-2 mg/kg IV over 5 minutes
  • Provides reducing agent to convert methaemoglobin back to haemoglobin

Management of Local Complications

  • Haematoma: apply pressure; monitor for expanding haematoma compressing nerves; rarely requires surgical evacuation
  • Infection: empirical antibiotics; drainage if abscess forms; be vigilant for deep space spread (fever, limited hip movement, pelvic/back pain after pudendal block - may be life-threatening)
  • Nerve damage: document baseline; conservative management; physiotherapy; most resolve within weeks to months; EMG/NCS if persistent
  • Phrenic nerve palsy: supplemental oxygen; patients with compromised respiratory reserve may require respiratory support
  • Failed block: supplement with additional infiltration, alternative regional technique, or proceed to general anaesthesia

Prevention of Complications

  • Always aspirate before injection (negative aspiration does not exclude intravascular placement 100% of time)
  • Use incremental, fractionated dosing for major blocks
  • Use lowest effective concentration and volume
  • Ultrasound guidance reduces vascular puncture and toxicity rates
  • Add epinephrine as a test dose marker (tachycardia within 30 seconds suggests intravascular placement)
  • Resuscitation equipment, oxygen, and appropriately skilled personnel must always be immediately available
  • 20% Intralipid must be stocked wherever major blocks are performed

Sources: Bailey & Love's Short Practice of Surgery 28th ed. | Miller's Anesthesia 10th ed. | Barash Clinical Anesthesia 9th ed. | Morgan & Mikhail's Clinical Anesthesiology 7th ed. | Fitzpatrick's Dermatology | Pfenninger & Fowler's Procedures for Primary Care | Schwartz's Principles of Surgery 11th ed.

Medicines to take after ovulation phase to avoid fertilization

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Medicines to Avoid Fertilisation After Ovulation (Emergency Contraception)

Important clarification: The question asks about post-ovulation contraception. It is important to understand that most emergency contraceptive (EC) medicines work by delaying or inhibiting ovulation - they are most effective before ovulation occurs. Once ovulation has already happened, their effectiveness drops significantly. This is a key clinical fact explained below under each drug.

Overview

Emergency contraception (EC), commonly called the "morning after pill," is used to prevent pregnancy after unprotected or inadequately protected intercourse. There are currently three oral options and one non-oral (IUD) option.

1. Levonorgestrel (LNG) - Progestin-Only Pill

Brand names: Plan B, Postinor-2, i-pill, Unwanted-72
Dose:
  • Single dose: 1.5 mg (preferred - simpler and equally effective)
  • Two-dose regimen: 0.75 mg, repeated 12 hours later (FDA-approved but less convenient)
Timing:
  • Labeled for use up to 72 hours after intercourse
  • Can be extended to up to 120 hours (WHO recommendation), but effectiveness declines after 72 hours
Mechanism:
  • Primary action: delays or inhibits ovulation (delays the LH surge)
  • Research by Noe et al. established that levonorgestrel only works if administered before the day of ovulation
  • No pregnancies occurred in 87 women who received LNG 1-5 days before ovulation
  • 7 pregnancies occurred in 35 women treated on the day of ovulation or after
  • It is NOT an abortifacient - it has no effect once fertilisation has occurred
Effectiveness: Pregnancy rate ~1.1% when taken within 72 hours
Side effects:
  • Nausea (23% vs 50% with estrogen combinations)
  • Vomiting (5.6%)
  • Irregular menstrual bleeding (resolves within 1 month without treatment)
  • Headache
Availability: Available without prescription in many countries (since 2013 in the US)
Limitation - Obesity:
  • Significantly reduced effectiveness in women with BMI >30
  • Total plasma concentration of LNG is significantly lower in obese women
  • For obese women, ulipristal is preferred over levonorgestrel
Starting regular contraception after LNG: Can start hormonal contraception immediately after levonorgestrel.

2. Ulipristal Acetate (UPA) - Progesterone Receptor Modulator

Brand name: Ella, EllaOne
Dose: Single tablet of 30 mg
Timing: Effective up to 120 hours (5 days) after intercourse - this is its key advantage over LNG
Mechanism:
  • Delays follicular rupture - when ovulation is imminent (pre-LH peak), UPA delays the preovulatory follicle rupture for 5 days or more
  • More effective than LNG at the periovulatory phase (when ovulation is imminent)
  • When administered prior to the LH peak, it is 42% more effective than LNG at 72 hours, and 65% more effective in the first 24 hours
  • Like LNG, it is not an abortifacient
Effectiveness: Pregnancy rate ~1.3% (vs 2.0% for LNG in a head-to-head RCT of 2,065 women)
Side effects: Similar to levonorgestrel - nausea, headache, irregular bleeding
Availability: Prescription-only
Advantage over LNG in obese patients: Plasma concentration of UPA is similar in both obese and normal-BMI women, making it more reliable in this group.
Drug interactions: Metabolised by CYP3A4 - drugs that induce CYP3A4 (barbiturates, rifampicin, anticonvulsants such as phenytoin, carbamazepine) can reduce UPA's effectiveness.
Starting regular contraception after UPA: Must wait 5 days before starting hormonal contraception - starting a progestin-only pill the day after UPA increased ovulation occurrence to 45% (vs 3% with placebo).

3. Combined Oral Contraceptive (Yuzpe Regimen) - Now Largely Obsolete

Dose: 100 mcg ethinyl estradiol (EE) + 0.5-1.0 mg levonorgestrel, taken twice 12 hours apart
Timing: Within 72 hours
Mechanism: Combined estrogen-progestin effect on ovulation inhibition
Why it fell out of favour:
  • Much higher rates of nausea (50.5% vs 23.1% with LNG alone)
  • Much higher rates of vomiting (18.8% vs 5.6%)
  • Several case reports of thrombotic events (not seen with LNG alone)
  • Inferior efficacy: pregnancy rate 3.2% vs 1.1% with LNG alone (RR 0.32)
  • Replaced by LNG alone and then ulipristal

4. Copper Intrauterine Device (Cu-IUD) - Most Effective Method

Type: Copper T380A is the most studied device for EC
Timing:
  • Effective within 5 days of intercourse (essentially 100% effective)
  • Also effective up to 7 days after intercourse
Mechanism: Works differently from oral options:
  • Inhibits sperm function (copper ions are spermicidal)
  • Inhibits transport of fertilised egg
  • Likely inhibits implantation
  • Does not require pre-ovulatory timing - works even after ovulation and potential fertilisation (this makes it the most effective EC option post-ovulation)
Effectiveness:
  • Pregnancy rate in the multicenter Wu et al. trial: 0 pregnancies in 1,893 women at follow-up
  • Efficacy ~100% when inserted within 5 days
Advantages:
  • Most effective EC available
  • Also provides ongoing long-term contraception (94% of women continued using it at 12 months)
  • Not affected by body weight
Disadvantages:
  • Requires a clinic visit and a qualified provider for insertion
  • 1/1,000 risk of uterine perforation
  • Uterine cramping after insertion
  • Not suitable for women with contraindications to IUD (active pelvic infection, uterine abnormalities, allergy to copper/Wilson's disease)

Summary Comparison Table

FeatureLevonorgestrel 1.5 mgUlipristal 30 mgYuzpe RegimenCopper IUD
Time windowUp to 72 h (120 h off-label)Up to 120 hUp to 72 hUp to 5-7 days
Pregnancy rate~1.1%~1.3%~3.2%~0%
MechanismDelays ovulationDelays ovulation (stronger at LH peak)Delays ovulationSpermicidal + anti-implantation
Post-ovulation efficacyNoneMinimalNoneYes
Prescription neededNo (most countries)YesNoYes (procedure)
Obesity effectReduced efficacyNot affectedReducedNot affected
Main side effectsNausea, spottingNausea, spottingHigh nausea/vomitingCramping, perforation risk

Critical Clinical Point

If ovulation has already occurred, oral EC pills (LNG and UPA) are not effective. Research clearly shows LNG has zero benefit when taken on or after the day of ovulation. UPA has marginally more activity at the periovulatory window but is similarly ineffective once ovulation is complete. The copper IUD is the only reliable option if intercourse occurred post-ovulation, as its mechanisms of action work after ovulation occurs.

Sources: Berek & Novak's Gynecology | Rosen's Emergency Medicine | Tintinalli's Emergency Medicine | Textbook of Family Medicine 9th ed.
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