Anaesthesia - principles Flashcards
Types of anaesthesia
general - producing insensibility in WHOLE BODY, usually causing UNCONSCIOUSNESS - CENTRALLY ACTING DRUGS (hypnotics/analgesics)
regional - producing insensibility in AREA/REGION of body - LA APPLIED to NN. SUPPLYING RELEVANT AREA
local - producing insensibility in ONLY RELEVANT PART of BODY - LA APPLIED DIRECTLY to TISSUES
Balanced anaesthesia
- DIFFERENT DRUGS do DIFFERENT JOBS
- TITRATE DOSES SEPARATELY + therefore, MORE ACCURATELY to REQ.
- AVOID OVERDOSAGE
- ENORMOUS FLEXIBILITY
Problems
- POLYPHARMACY - increased risk of drug reactions, allergies
- MUSCLE RELAXANTS - NOT SEDATIVE, NOT ANALGESIC - req. for artificial ventilation for airway control
- SEPARATION of RELAXATION & HYPNOSIS - awareness (pt. paralysed but awake)
GA: how do they work
• INTERFERE W/ NEURONAL ION CHANNELS in DOSE DEPENDENT FASHION - HYPERPOLARISE NEURONES (opens chloride channels/suppresses excitatory synaptic activity)
* INHALATIONAL = DISSOLVE IN MEMBRANES (direct physical effect) * IV = ALLOSTERIC BINDING (GABA receptors - open chloride channels)
• IF PROCESS REQUIRES MORE ION CHANNELS = MORE LIKELY TO LOSE IT EARLY (tend to be COMPLEX PROCESSES e.g. LOC 1ST, HEARING LATER, PRIMITIVE FUNCTIONS EVEN LATER, REFLEXES RELATIVELY SPARED - primitive + small no. of synapses - cerebral function lost top down)
GA: effects on physiology
CVS:
* CENTRAL = DEPRESS CV CENTRE (reduces symp. outflow + -ve inotropic/chronotropic effect on heart + reduced vasoconstrictor tone - vasodilation) * DIRECT = -VELY INOTROPIC, VASODILATION due to decreased peripheral resistance, VENODILATION due to decreased VR and decreased CO
RESPIRATORY:
* ALL ANAESTHETIC AGENTS (except ketamine) = RESPIRATORY DEPRESSANTS = REDUCE HYPOXIC + HYPERCARBIC DRIVE, DECREASED TIDAL VOL. + INCREASED RATE * PARALYSE CILIA * DECREASE FRC (functional residual capacity) = LOWER LUNG VOL., VQ MISMATCH
GA: in practice
- ABC - LONG DRAWN OUT RESUSCITATION
- MANDATES AIRWAY MANAGEMENT - IMPAIRMENT of RESPIRATORY FUNCTION & BREATHING CONTROL
- CV IMPACT
- CARING for UNCONSCIOUS PT.
- IV = RAPID ONSET of UNCONSCIOUSNESS + RAPID RECOVERY
- Rapid onset of consciousness - 1 arm-brain circulation; highly fat soluble drugs so cross membranes v. quickly + leave circulation v. quickly is given as one-off dose as moves into other body cpts.
- Rapid recovery - disappearance of blood from circulation due to redistribution, metabolism has little impact
- HEPATIC METABOLISM + RENAL EXCRETION
- INHALATIONAL = UPTAKE & EXCRETION via LUNGS; SLOW INDUCTION, ANAESTHESIA MAINTENANCE, AWAKENING
- HALOGENATED HYDROCARBONS
- UPTAKE + EXCRETION via LUNGS - gas moves down conc. Barrier from lungs - blood - brain, crosses alveolar BM easily, arterial conc. = alveolar partial pressure (equates quite closely)
- MAC - minimum alveolar conc., measure of potency (low number means high potency)
- INDUCTION - SLOW
- MAINTENANCE - PROLONG DURATION, V. FLEXIBLE
- AWAKENING - STOP INHALATIONAL ADMINISTRATION, WASHOUT - REVERSAL of CONC. GRADIENT
Muscle relaxants: how do they work
- INDISCRIMINANTLY PARALYSE SKELETAL MUSCLE incl. those of RESPIRATORY + AIRWAY
- SYSTEMIC MUSCLE RELAXANT - MUST GIVE HYPONOTIC DRUG (paralysed but awake is extremely uncomfortable)
Muscle relaxants: in practice
INDICATIONS:
- VENTILATION + INTUBATION
- IMMOBILITY ESSENTIAL - microscopic surgery, neurosurgery
- BODY CAVITY SURGERY (access)
PROBLEMS:
- AWARENESS - separation of unconsciousness from hypnosis, paralysed but awake
- INCOMPLETE REVERSAL - airway obstruction, ventilatory insufficiency in immediate post-op period
- APNOEA - dependence on airway + ventilatory support
- MAINTAIN + PROTECT AIRWAY while in effect - otherwise death
LA + regional anaesthesia: how do they work
- BLOCK Na+ CHANNELS - PREVENTS AXONAL AP from PROPAGATING
- DIFFERENTIAL BLOCKADE due to DIFFERENTIAL PENETRAITON into DIFFERENT TISSUE TYPES
- MYELINATED THICK FIBRES - RELATIVELY SPARED e.g. motor fibres
- PAIN FIBRES BLOCKED EASILY
LA + regional anaesthesia: effects on physiology
- RETAIN AWARENESS/CONSCIOUSNESS
- LACK of GLOBAL EFFECTS of GA
- DERANGEMENT of CVS PHYSIOLOGY - proportional to size of anaesthetised area
- RELATIVE SPARING of RESPIRATORY FUNCTION - may be preferred in pt. w/ respiratory co-morbidities, only relative effect - are consequences for respiratory system in regional techniques
CVS: NEURAXIAL BLOCK
• Similar to CVS effects of GA (venodilation + arterial vasodilation) BUT ALL RA EFFECTS DUE TO SYMPATHECTOMY because of LA BLOCKAGE of MIXED SPINAL NN. ○ Effects limited to region of body covered by block - greater area covered results in greater physiological impact
RESPIRATORY: NEURAXIAL BLOCK - effects via LA block of mixed spinal nn.
* INSPIRATORY FUNCTION RELATIVELY SPARED - unless high block * EXPIRATORY FUNCTION RELATIVELY IMPAIRED - cough dependent on abdo muscle function * DECREASE FRC - AIRWAY CLOSURE comparable to GA * INCREASED V/Q MISMATCH
LA + regional anaesthesia: in practice
LA PROBLEMS:
* TOXICITY!! - limits use * TOXICITY - HIGH PLASMA LVLS e.g. in IV INJECTIONS; ABSORPTION > RATE of METABOLISM - resulting in HIGH PLASMA LVLS - well-perfused areas have higher absorptions - VASOCONSTRICTORS reduce blood flow and therefore, reduce absorption * TOXICITY depends on: DOSE USED, RATE of ABSORPTION (site-dependent), PT. WGT., DRUG (bupivacaine > lignocaine > prilocaine)
PRESENTATION of LA TOXICITY: from earliest and least toxic
* CIRCUMORAL + LINGUAL NUMBNESS and TINGLING * LIGHT-HEADEDNESS * TINNITUS, VISUAL DISTURBANCES * MUSCULAR TWITCHING * DROWSINESS * CV DEPRESSION * CONVULSIONS * COMA * CARDIORESPIRATORY ARREST