Misc Flashcards
In which neuromuscular condition can sux be used safely?
Myasthenia gravis and in fact may need 2x normal dose
However in ELS need to use a reduced dose although again can be used
In which conditions must you avoid anti cholinesterases and why?
Myotonic dystrophy and myotonic congenita
Can lead to hyperkalaemia
Myasthenia gravis - can actually prolong block and lead to cholinergic crisis
Myotonic dystrophy and myotonic congenita inheritance
Both autosomal dominant
MD - chromosome 19
MC - chromosome 17
Drugs to avoid in patients with prolonged QT
Ketamine
Suxamethonium
Methadone
Most antiemetics but not cyclizine or dex
Oxytocin
Macrolides
Avoid anticholinergics and adrenergic drugs - CAN use meteraminol and phenyl safely however
Systemic sclerosis/Scleroderma features
Limited scleroderma - CREST
Calcinosis, Raynauds, oesophageal dysmotility, sclerodactyly and telangectasia
Most concerning complications of systemic sclerosis (responsible for most mortality)
Pulmonary fibrosis
Myocardial disease
PAH
What is systemic sclerosis
A rare autoimmune condition leading to inflammation and progressive multi system connective tissue disease
Small vessel vasculopathy and abnormal collagen deposition leading to fibrosis of skin and organs
Risk factors for abnormal placental adherence
Placenta praevia
Previous C section
IVF
Advanced maternal age
Previous endometrial surgery Ie myomectomy or ablation
Multiparity
Ashermans syndrome
Classes of chemotherapy agents
See photo
Functions of the spleen
Drugs used in Parkinson’s
NAP 5 findings
What operations are highest risk for CPSP?
Amputation
Thoracotomy
Mastectomy
Cholecystectomy
Inguinal hernia
Vasectomy
Caesarean
Safety re ABO compatibility for transfusion of FFP/cryo/platelets
FFP and cryo should be ABO compatible ideally but if not possible, AB is universal donor, Rh compatibility is not required
Platelets should ideally be ABO compatible but any can be used in emergency, just may not see such good increment
What is Marfans
Autosomal dominant disorder
Connective tissue disorder
Defect in fibrillin 1 gene on chromosome 15
Clinical features of marfans
Criteria for CRT device
NYHA classification class III or IV
Patient in sinus rhythm with wide QRS(ie LBBB) or normal QRS with vent dyssynchrony on ECG
EF < 35%
Already on max medical therapy
Symptoms of TCA overdose
Hypotension
Tachycardia
ECG changes inc wide QRS
Cardiac depression
Vent arrhythmias
Mydriasis
Reduced consciousness
Hyperreflexia
Seizures
MOA of TCAs
Inhibition if pre-synaptic reuptake of noradrenaline and serotonin
Packed red cells storage
- temp and solution
4 degrees to inhibit bacterial growth and reduce RBC energy use
Solution - usually citrate, phosphate, dextrose and adenine
Citrate prevents clotting and phosphate is a buffer
Others are nutrients
Store - for up to 35 days
FFP storage
-20 degrees
Use immediately when thawed
AB is universal donor
Cryo storage
-30 degrees for up to 1 year
Contains high levels of factor 8, vWF and fibrinogen
AB is universal donor
What is in prothrombin complex concentrate and when to give it
Clotting factors 2/7/9/10 and protein C and S
For reversal of raised INR in bleeding patient on warfarin
Platelet storage
At room temp (22degrees) for up to 5 days with continuous agitation to avoid clumping
Ideally ABO matched but can use any
Transfusion reaction associated lung injury
What are the nervous system changes in the development of phantom limb pain/neuropathic pain
- in peripheral/spinal cord and central NS