UW Flashcards
Drugs for neuropathic pain
- TCA (be careful in older because anti-cholinergic)
- anticonvuslants (gabapentin, pregabalin) (BEST)
- opioids
- capsaicin tpical
- lidocaine topical
consider anticonvulstants or TCA for initial
radioablation for graves - SE
- permanent hypothyroidism over months to years (resolution of hyperth in 6-18 wks) (this is not happening in toxic adenoma or goiter because only the adenomas take iodine)
- worsening of Graves opthalmopathy due to increased of TSI (if mild: give steroids, if severe: prefer surgery)
Diagnostic approach of hypocalcemia
low Mg, medications, Recent blood transfusion (citrate)?
- YES –> correct it
- NO –> measure PTH
low: surgical, autoimmune, infiltrative (metast, wilson, hemochromatosis)
high: vit d def, renal failure, pancreatitis, sepsis, tumor lysis syndrome
hyperthyroidism with high TSH and high hormones - next step
brain MRI
hyperthyroidism with low TSH and high hormones - next step
graves signs (goiter, ophtalmopathy)?
- yes –> graves
- NO RAIU
high uptake: graves or nodular or adenoma
low uptake: measure thyroiglobulin (low: exogenous hormone, high: thyroditis or iodide exposure)
hyperthyroidism effect on BP
increased Myocardial contractility
decreased peripheral resistance
(in contrast, hypothyroidism causes hypertension due to increased peripheral resistance)
PAC/PRA ratio
- plasma aldosteron / plasma renin concentration
- 1st test for hypertension and hypokalemia
best initial test for patient with DM and new toe ulcer
monofilament (it predicts the risk of future ulcers: higher pressure threshold)
toe ulcer - vascular or DM
arterial are usually on the tips
DM: plantar
diagnosis of hypercalcemia
- confirm it (repeated tests + correct for albumin)
- measure PTH
- if low PTH: measure PTHrp, vitD25, vitD1,25
MCC of PTH-independent malignancy
homural hypercalcemia of malignancy (PTHrp)
PTHrp does not induce Vit D activation
a cause of hypercalcemia after accidents
immobilization (PTH independent) due to inccreased osteoblastic resorption
(4 weeks after immobilization, but in 3 days in patients with chronic renal failure)
treatment: biphosphanates
MCC of death in acromegaly
cardiovascular disease
but decreasing of the levels rapidly reduces the risk
euthyroid sick syndrome
any patient with acute severe illness may have abnormal thyroid function test
NORMAL TSH AND T4
fall in total and free t3
acute vs chronic thyrotoxic myopathy
acute: severe distal or proximal weakness, without bulbar or resp involvement
chronic: proximal
DDX for hyperandrogenism in women
- PCOS 2. Acromegaly 3. Cushing
- Hyperprolactinemia 5. ovarian/adrenal tumors
- Non-classic CAH
hypomagnesimia mediated hypoparathyroidism vs other causes of hypoparathyroidism
hypoparthyroidism associated with low Mg has normal or low P
milki alkaly syndrome
it is caused by excessive intake of calcium and absorable alkali. It can be seen in patient taking calcium bicarbonate for osteoporosis.
manifestation: symptomatic hypercalcemia, met alkalosis, acute kidney injury
thionamides - agranoulocytosis
routine WBC check it is not cost effective
- if fever + sore throat –> stop the drug and check the WBCs
if less than 1000 –> stop permanently
if more than 1500 –> it is not the cause
DM2 - when to add insulon to metformin
when HBAC1 is more than 8.5%
the MC electrolytic abnormality in primary adrenal insufficiency
hyponatremia in 90%
following cortisol discontinuation, the axis me be abnormal up to
6-12 months
suppurative (infectious) thyroditis
fever erythema and severe pain, often with asymmetric goiter due to abscess formation (usually in children and immunocompromised)
USUALLY EUTHYROD
the main substance for gluconeogenesis
alanine (from proteins breakdown), glutamine (from proteins breakdown), lactate (from anaerobic), glycerol-3-P (from lipids break down)
alanine is converted into …. during gluconeogenesis
pyruvate
clinical suspicion of acromegaly - algorithm
measure IGF-1 - normal (exclude) - elevated --> oral glucose suppression test adequate GH suppression --> exclude inadequate GH suppression --> BRAIN MRI if pituitary mass --> surgery if no mass --> search for other source
metabolic syndrome - features
3 out to 5
- abdominal obesity (waist more than 40 in males and 35 in females
- fasting glucose more than 100-110
- BP more than 13/8
- TG more than 150
- HDL cholesterol lower of 40 in male and 50 in women
how to measure corrected calcium
calcium + 0.8 (4-serum albumin)
VIPoma - clinical presentation
- watery diarrhea
- hypo or achrolorhydia due to low gastric acid secretion
- flushing, lethargy, nausea, vomiting, muscle wekaness
PANCREATIC CHOLERA
VIPoma Labs
- low K+
- high Ca2+
- high hyperglycemia (increased glycogenolysis)
- diarreha: increased sodium + osm gap less than 50
VIPoma - diagnosis
- watery diarrhea with VIP level more than 75
2. abdominal CT or MRI
Difference in labs between insulinomas and sulfonylurea
in sulfo, the proinsulin is less than 20% of the total insulin immunoreactivity
the diagnosis is confirmed by sulfonylurea measurement
severe SE caused by PTU (but not by methimazole
- hepatic failure
2. ANCA mediated vasculitis
in which situations, thyroidectomy is prefered against RAI for Graves
- very large goiter
- severe ophtalmopathy
- coexisting nodule and suspicion for malignancy
- pregnant who cannot tolerate drugs
- coexisting 1ry hyperpara
- obstructive symptoms
x-ray findings of osteomalacia
- decreased bone density with thining of cortex
- eventual codfish vertebral bodies (concave shape)
- pseudofractures (Looser zones)
screening for DM is recommended in ….
- patients with sustained BP more than 135/80
- may considered in all patients over age 45
- additional risk for DM
osteolytic metastasis can cause hypercalcemia - mechanism
stimulation of osteoblast by cytokine production
paroxysms of severe hyperteneion in pheo can be precipitated by
increases in intra-abdominal pressure (tumor palpation, position changes etc), surgical procedures, and a number of drugs, especially anesthetics