ANAESTHESIA C (26) Flashcards

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1
Q

CVC LENGTHS AT SKIN?

A
  • Both SC and IJ are the same at
    • R = 16cm
    • L = 20cm
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2
Q

WHAT GAUGE ARE TRIPLE LUMEN CVC LINES?

A
  • The brown lumen is 16g, the other 2 are 18g
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3
Q

IDEAL POSITION OF A CVL

A
  • in the SVC, with the tip 2cm proximal to the RA
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4
Q

WHAT IS ABDOMINAL COMPARTMENT SYNDROME?

A
  • Normal Intra-Abdominal pressure is <10mmHg, and can be easily measured with a sensor in a bladder catheter
  • Systemic increases in capillary permeability, eg in trauma, sepsis or large burns, can cause massive oedema fluid accumulations in the peritoneal cavity, mesentery, gut wall and retroperitoneum
  • this can cause increases in Intra-Abdominal pressure, or ‘Abdominal Hypertension’, which, if >20mmHg, progressively impairs ventilation, cardiac output and renal function
  • MANAGEMENT
    • address the cause
    • dont over resuscitate
    • consider decompressive laparotomy
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5
Q

DERMATOMES

A
  • C2 = collar
  • C3 = above clavicles
  • C4 = below clavicles
  • C5678T1 = arms
  • T2 = interaxillary
  • T4 = nipple
  • T6 = xiphoid
  • T10 = umby
  • T12 = belt
  • L1 = groin crease
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6
Q

SPINAL DOSES USING 0.5% HEAVY MARCAIN

A

There are 2 does, high and low

  • for a high (T4) block :
    • 2.5 mls for LSCS
    • 4.0 mls other
  • for a low (T10) block (hips/urology)
    • 2.5 mls
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7
Q

WHAT LA TO USE FOR PERIPHERAL NERVE CATHETERS?

A
  • ROPIVACAINE 0.2%, 5-10 ml/h
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8
Q

MAXIMUM LA DOSES

A
  • LIGNOCAINE = 5mg/kg, 7 with Adrenaline
  • BUPIVACAINE = 2mg/kg, 3 with Adrenaline
  • ROPIVACAINE = 3mg/kg
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9
Q

HEPARIN WITHOLDING TIMES FOR INSERTING SPINALS/EPIDURALS

A

Coags must be normal for insertion, so hold:

  • IV HEPARIN: 4h
  • S/C HEPARIN/CLEXANE: 12h
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10
Q

WHEN CAN YOU GIVE HEPARIN AFTER SITING A SPINAL/EPIDURAL

A
  • It is generally safe to give SC Heparin immediately, and IV 1h after atraumatic insertion
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11
Q

VASCULAR STENTS : BARE METAL vs DRUG ELUTING AND SURGERY

A
  • Traditionally, stents were BARE METAL (BMS), which epithelialised rapidly, but had poor long term patency.
  • Newer stents are DRUG ELUTING (DES), which epithelialise more slowly, giving better long term patency, but require long term antiplatelet* therapy.
  • PERIOPERATIVE MANAGEMENT:
    1. Acutely stopping antiplatelet Drugs perioperatively is DOUBLY RISKY because:
      • Surgery is a pro-coagulant state
      • ‘rebound stickiness’ occurs …. so
    2. defer elective surgery 3/12 for BMS and 12/12 for DES
    3. stop PLAVIX but continue Aspirin preop

*NOTE: it is ANTI-PLATELET therapy that is needed for stents, - remember this as the platelet is the FIRST part of clot formation. Anticoagulants like HEPARIN/CLEXANE have little protective benefit

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12
Q

PACEMAKERS AND ICDS AND SURGERY

A

The main issue is that diathermy noise may be interpreted as either

  1. appropriate cardiac activity : causing inhibition of pacing, or
  2. VT/VF : causing inappropriate shock

Previously we used to switch devices to a non sensing ‘SAFE’ mode preoperatively, but modern units now discriminate so well we generally just have a pacemaker magnet available intra-operatively

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13
Q

ANAPHYLAXIS BLOODS

A
  • Take MAST CELL TRYPTASE at 1, 4 & 24 hours
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14
Q

TROPONIN esp TROPONIN-T

A
  • TROPONIN is a contraction regulating protein found in both cardiac and skeletal muscle.
  • Assay of one variant, MYOCARDIAL TROPONIN-T (Trop-T) is a sensitive and specific test for myocardial injury, but
    • it rises slowly : may take 12h
    • interpretation of modest rises is uncertain in CRF
  • [Trop-T] > 100 is Positive
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15
Q

NORMAL RENAL FUNCTION =

A
  • Urine output of 0.5 ml per kg per hour
  • N electrolytes
  • Urea 3-8 mmol/l
  • Creat 50-120 umol/l
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16
Q

HYPERKALEMIA : EFFECTS AND TREATMENT

A
  • Normal ECF K+ = 3.5 - 4.5
  • Hyperkalemia increases cellular irritability by partly depolarising the cell membrane, producing ECG changes:
    • at 7.0 : peaked T
    • at 8.0 : wide QRS and no P
    • at 9.0 : sinusoidal ecg then VF

Rx:

  • ultimately need to eliminate excess K+ by RESONIUM/Dialysis,
  • but in the interim may SHIFT it back into the cells by giving:
    • ACTRAPID 5u IV (+ 50 mls 50%D) or
    • HCO3- : 1mlkg 8.4%
  • or STABILISE the cell membrane with CaCl: 10 mls x 10%
17
Q

WHY IS CA CHLORIDE PREFERRED OVER CA GLUCONATE?

A

Because:

  1. CaCl contains 3x more Ca than CaGluconate
  2. Ca Gluconate needs to be hepatically metabolised before the Ca becomes available
18
Q

pO2 vs SpO2

A

50/60/70 mmHg = 85/90/95 % saturated

19
Q

WTF IS BASAL BOLUS INSULIN?

A

the BASAL BOLUS INSULIN regime is a more physiological way of giving Insulin than the Actrapid SS, dividing the daily insulin prescription into

  1. a long acting BASAL insulin dose (LANTUS) given nocte
  2. 3 equal short acting BOLUS doses given with meals (NOVORAPID)

METHOD

  1. write “Insulin : see basal bolus chart” in drug orders
  2. estimate daily Insulin requirements as either
    • 0.4u/kg/d if not previously on Insulin
    • usual 24h units if already on Insulin
  3. give 1/2 the units as LANTUS at 2100, and 1/2 as 3x equal mealtime doses of NOVORAPID
  4. check BSL before each dose and consider adjusting previous or pending dose
20
Q

SGLT2 INHIBITORS, EUGYLCAEMIC DKA AND PERIOPERATIVE MANAGEMENT

A
  • SGLT2 Inhibitors like Dapagliflozin* increase urinary excretion of glucose by inhibiting the ‘Sodium-Glucose Transporter’ pumps which reabsorb filtered glucose from the renal tubule.
  • They can cause perioperative ‘euglycaemic DKA’ and should be stopped 2/7 prior, and still require postop blood sugar, pH and ketone monitoring - the wards can now do this.
  • Where not held:
    • For minor surgery: go ahead.
    • For major surgery: go ahead, provided:
      • HbA1C <9 and ketones <0.6
      • Insulin infusion commenced after
      • Endocrinology team notified

* ‘fear the flozins’

21
Q

WHAT IS SITAGLIPTIN?

A
  • Sitagliptin, aka Januvia, increases insulin levels by boosting the insulin releasing hormones secreted by the gut in response to a meal.
  • As such, it is relatively self regulating and has a low risk of hypoglycaemia.
22
Q

WHAT IS DIABETES INSIPIDUS, AND HOW TO MANAGE?

A
  • DI = excessive production of DILUTE URINE, usually due to loss of ADH (VASOPRESSIN) secretion from the PITUITARY, eg after head injury
  • the result is a dilute polyuria, dehydration and hypernatremia (Na >150)
  • Rx : address the dehydration, and replace vasopressin with either:
    • DDAVP 6-12 mcg
    • VASOPRESSIN, 20u in 40mls, 1ml stat then 4-0 ml/h
23
Q

VASOPRESSIN vs DDAVP

A
  • VASOPRESSIN is a posterior pituitary hormone which defends the BP by
    • Retaining water at the kidney
    • Vasoconstricting
    • Boosting F8 and platelet function
  • DDAVP is a modified synthetic vasopressin which retains its antidiuretic and procoagulant effects, but is not vasoconstrictive. Its mainly used for DI and haemophillia
24
Q

WHAT IS SIADH?

A
  • SIADH = the Syndrome of Inappropriate ADH secretion, where VASOPRESSIN is inappropriately secreted from an ectopic focus, eg a lung tumour
  • it results in inappropriate water retention by the kidney, with volume overload and dilutional Hyponatremia (<120)

Rx:

  • address the cause if possible
  • fluid restriction
25
Q

100mmHg = x cm H2O?

A
  • 100 mmHg = 130 cm of water (or blood)
26
Q

WHAT IS THE HEARTS NORMAL EJECTION FRACTION?

A
  • The Normal EF = 50 - 75%