Medicine Flashcards
(147 cards)
Thyroid nodules
Work up
Hot vs Cold
Evaluate labs
1st step: TSH & US
- If RF or sus US (microcalcification, increase vascularity, hypoechoic, indistinct nodule margins) –> FNA
- If no RF & normal US –>
——-Normal or High TSH: FNA
——-Low TSH: Iodine 123 scintigraphy
Hot/Hyperfunctioning: treat
Cold/Hypofunctioning: FNA
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Evaluating labs values
1: measure TSH, Free T3 and T4
If primary labs (low tsh, high t3/t4)—> does the patient have signs of Graves?
Yes? Graves
No? Radioactive iodine uptake
—— High: graves, toxic adenoma, multinodular goiter
—— Low: Thyroiditis, Iodine exposure, exogenous
Thyroglobulin levels will be low with exogenous use
Thyroglobulin levels will be high if gland has lots of activity
If secondary labs (high tsh and t3/t4) –> MRI of pituitary gland
Goiter can be caused by iodine deficiency which are mostly multinodular, and should be surgically removed
Thyroid cancer
Dx, Tx, Pemberton test
1st step: US neck and LN
If <1cm: lobectomy
If >1cm: Thyroidectomy +/- radiation
Pemberton test: raise arm over head for 60 sec –> facial plethora or engorgement of neck veins is suggestive of thyroid source
Thyroglossal duct cyst
Sx, Dx Tx, Comp if not Tx
- Tenderness and pain is often preceded by URI
- Associated with ectopic thyroid tissue (may be the only site for functioning tissue).
Dx: US or CT
Tx: resection of cyst, associated tract and central portion of hyoid bone.
Comp if not resected:
- Recurrent infection.
- Cyst are benign and do not under malignancy transformation. Rarely, patients may develop thyroid cancer from ectopic thyroid tissue WITHIN the cyst, but not from malignant degeneration of the cyst itself.
Gout
What does it look like, Tx
Pseudogout
What does it look lik
Gout
Needle-shaped, Negative birefringent
Tx: 1st line - NSAIDs (indomethacin), colchicine
2nd line: Steroids
Allopurinol: decrease uric acid production –> prevent flares
Pseudogout aka calcium pyrophosphate deposition disease
Rhomboid-shaped, weakly ⊕ birefringent under polarized light (blue when parallel to light)
Acute tx: NSAIDs, colchicine, glucocorticoids.
Prophylaxis: colchicine
Conn Syndrome
2 causes, Sx, Dx, Tx
High Aldosterone d/t
1. B/L adrenal hyperplasia (idiopathic)
2. Unilateral adenoma (most common- Conn syndrome)
Sx:
- Difficult to control hypertension
Dx:
- Elevated plasma aldosterone & low plasma renin
- Hypokalemia, low H+ –> metabolic alkalosis
- Increased na reabsorption –> HTN –> increased renal blood flow & GFR –> increase na excretion therefore, NA IS UNCHANGED
- Absence of aldosterone suppression with oral saline load
- CT scan of adrenal glands
Tx:
- Bilateral adrenal hyperplasia: mineral corticoid receptor antagonist (spironolactone)
- Unilateral adenoma: surgical resection
Cushing syndrome
3 causes, Sx, Dx
High cortisol d/t
1. exogenous –> low ACTH
2. Adrenal adenoma, hyperplasia/carcinoma –> low ACTH
3. ACTH secreting pit adenoma aka Cushing Disease –> high ACTH
Sx: HTN, hyperglycemia, mood swings, osteopenia/osteoporsis, aldosterone-like effect (low K and metabolic alkalosis)
Dx: 24hr urinary free cortisol level or 1mg overnight dexamethasone test – should suppress ACTH –> suppress cortisol
Adrenal insufficiency
Primary, secondary, tertiary causes, Sx, Tx
Inability of adrenal glands to generate enough glucocorticoids +/− mineralocorticoids for the body’s needs.
Primary: Deficiency of aldosterone and cortisol production due to loss of gland function. Acute or Chronic aka Addison.
Skin and mucosal hyperpigmentation
Secondary: Seen with decreased pituitary ACTH production. no skin discoloration and no hyperkalemia (RAAS intact)
Tertiary: Seen in patients with chronic exogenous steroid use, precipitated by abrupt withdrawal.
Sx: Weakness, fatigue, orthostatic hypotension, muscle aches, weight loss, GI disturbances, sugar and/ or salt cravings.
Tx: glucocorticoid/ mineralocorticoid replacement.
Adrenal mass management
Common but require workup for hormones hypersecretion or malignant
1. serum electrolytes
2. Dexamethasone suppression testing
3. 24hr urine catecholamines, metanephrine, vanillylmandelic acid
4. 17-ketosteroid
Surgical excision is recommended for all functional tumors, all malignancy tumors and all tumors >4cm
A fib
EKG finding, RF, Tx, Comp,
Postop Afib
Irregular, irregular with No p wave
RF: AGE (strongest) and comorbidities that cause atrial dilation (HTN, HF, mitral valve disease) , Can also be postoperatively.
Tx:
- Stable: Rate control with beta-blockers or non-dihydropyridine Ca channel blockers (diltiazem, verapamil)
- Unstable: Cardioversion
Comp: stroke
Most patients with no history of atrial fibrillation who develop POAF following cardiac surgery will spontaneously convert to sinus rhythm within a few days. However, such conversion to sinus rhythm does not signify resolution of atrial fibrillation and freedom from its associated complications. The development of POAF likely indicates substantial underlying substrate, and many patients will have re-occurrence of fibrillation, both during hospitalization and following discharge, placing them at risk for complications, including embolic, stroke and heart failure. This is also associated with increased long-term mortality.
Supraventricular tachycardia
Path, Sx, EKG, Tx
WPW (comp and tx)
- Secondary conduction pathway that allows abnormal cycling of cardiac conduction and formation of re-entrant circuit.
- Abrupt on set on palpitations
- EKG: narrow complex tachycardia with regular R-R intervals. P waves are usually inverted and often buried within QRS complexes
- Tx:
—Stable: vagal maneuvers, adenosine
—Unstable: urgent synchronized cardio version.
Association: WPW pattern + symptomatic tachyarrhythmia –> WPW syndrome
- Can also develop Afib –> syncope which is especially dangerous
Tx: Catheter ablation if syndrome occurs
Acute HF (Cause, Dx, Tx)
Chronic HF (Cause, Dx,Tx)
HF w/preserved EF (Def, RF, Tx)
Decompensated HF (factors to determine dx)
Acute HF
Most common cause: MI
Dx: TTE
Tx:
- O2
- IV diuretics (furosemide) or IV vasodilators (Nitroglycerin) to decrease preload –> decrease PCWP & reduced pulmonary edema
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Chronic HF
Causes:
- Most common: CAD –> ischemia
Dx:
- Echo
- Stress testing to r/o CAD
Tx:
Initial optimized therapy
1a. ACE’s & ARB’s: slows disease progression & improved mortality
1b. Beta blocker (Metoprolol, succinate, carvedilol, or bisoprolol): reduced hospitalization & improved mortality
1c. Diuretics +/- metolazone: improve sx & reduce hospitalization
2nd step of optimized therapy
2. Aldosterone antagonist (Spironolactone, Eplerenone, Amiloride, Triamterene): reduced hospitalization & improve mortality
3rd step in optimized therapy
3. SGLT-2 inhibitor: Reduce sx & improve mortality
Supplementary agents
4a. Isosorbide denigrate + hydralazine: Improve symptoms & may improve mortality
4b. Digoxin: reduced hospitalization but NO mortality benefit
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HF w/reserved EF
- Cause: LV dysfunction d/t impaired relaxation
- RF: chronic HTN, obesity, CAD
- Tx: spironolactone, SGLT2 inhibitors, Loop diurectics, Anti-HTN
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Decompensated HF
- Most important in the following order: S3 (MOST IMPORTANT) > orthopnea > crackles > JVD > LE edema > dyspnea
- Patient with slowly progressive decompensation may have minimal or no pulmonary edema because of increased lymphatic drainage.
Dystonia
What is it, Tx
Focal dystonia affects single muscle or a group of related muscles. Usually last specific
Can be triggered by increased sensory input (light, touch)
Can be temporarily relieved by sensory output as well
Oromandibular dystonia is an example
Focal: botulinum toxin (1st line)
Generalized: Carbamazepine
Back Pain
3 important things to look for + Dx
Uncomplicated vs Spondylolysis: Dx + Tx Rupture of anulus fibrosus presentation
Poor prognostic factors
Must always rule out serious disease with careful history.
1. Neurologic deficits (urinary/fecal issues, LE weakness)
2. Malignancy(cancer hx, wt loss, RF)
3. Infection (fever, midpoint spinal tenderness, immunosuppression) Ex Abscesss
Dx for above presentation: MRI
- Uncomplicated/Nonspecific:
Dx: Pain w/straight leg test suggest lumbosacral radiculopathy - Spondylolysis: overuse injury –> unilateral or bilateral fracture of pars interarticularis
Dx: pain worse with extension, tenderness with deep palpation, radiculopathy as slippage progesses - Rupture of anulus fibrosus leading to disc herniation: worse with flexion, positive straight leg test
Tx:
- Uncomplicated back pain: NSAIDs, heat therapy, massage, exercise .
Spondylolysis: rest for 90 days, allowing fracture to heal
Poor prognostic factors
- Advanced age
- Poor baseline functional status
- Severe self-rated pain & mood symptoms
Psychosocial factors:
- Psychiatric comorbidities (depression, anxiety)
- Maladaptive pain behavior (catastrophizing, avoidance behavior)
- Poor recovery expectations
Others:
- No interest in mobility/exercise (prolonged bedrest)
- Required opioid therapy to manage
Colon cancer
Screening times, RF
RF: Family hx. polyposis syndrome. IBD, African American race, alcohol intake, cigarette smoking, obesity
Screening
- Begins at 45y/o, then every 10 years
- Can do sigmoidoscopy every 5 years
If 1st degree relative has colorectal cancer or high risk adenomatous polyp
- Begins at 40y/o or 10 years prior to age of dx, repeat every 5 years
If you have UC: begin 8-10 years after dx, then every 1-3 years
Tx:
- Colonoscopy is most sensitive
- Flexible sigmoidoscopy is an acceptable alternative if average risk
Post ICU syndrome
Psych: >50% depression, PTSD, sleep disturbances
Neurocognitive: decrease attention/memory, executive function & processing speed
Physical: >50% have decreased mobility & independence
Most impairments last for several years, require chronic health services and are unable to return to work
Mesenteric ischemia
4 common main causes, Sx, Comp, Labs, Dx, Tx
Colonic ischemia
Occurs d/t decrease blood flow by
1. SMA occlusion d/t embolic disease
2. arterial and venous thrombosis d/t atherosclerotic disease and watershed infarctions
3. Hypercoagulable state
4. Hypovolemia
Sx. severe rapid abdominal pain but minimal tenderness (no guarding or rebound tenderness), N/V.
Comp: Can lead to abdominal distension, absent bowel sounds, peritoneal signs, bloody stool
Labs: anion gap metabolic acidosis d/t elevated lactate, and elevated amylase
Dx: CT angiography
Tx: IVF, Abx, NGT for decompression
Colonic ischemia: lateralized pain followed by blood stool, pain is mild/moderate
Hemorrhoids (internal vs external
Perianal vs Perirectal access (Dx, Tx, Comp)
Internal: painless – rubber band ligation, sclerotherapy, or infrared light application
External: painful and pruritic –> surgical
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Simple perianal abscess (be:
- Located within the dermis and subcutaneous tissue.
- Dx: PE
- Tx: I&D at bedside
Perirectal abscess:
- Deeper location, can cause systemic symptoms (fever, tachycardia).
- Dx: CT scan of pelvis w/contrast to confirm location and extent of infection.
- Tx: surgical drainage in OR w/ IV antibiotics
- Comp: fistula formation
Benign paroxysymal positional vertigo
Vertebrobasilar insufficiency
Labyrinthitis
Vestibular schwannoma
Meniere disease
Vestibular neuritis
What’s occurring, Sx, Dx, Tx (if any)
BPPV:
- Abnormal feeling of motion triggered by certain positions.
- Movement is sensed by semicircular canals which are filled by endolymphatic fluids.
Canalithiasis: presence of crystalline debris in the canals
Dx: Dix-Hallpike maneuver –> vertigo and nystagmus
Tx: Canalith repositioning maneuver (Epley)
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Vertebrobasilar insufficiency
- Reduced blood flow to the base of the brain that mainly affects labyrinth and brainstem
RF: DM, HTN, hypercholesterolemia, arrhythmia, CAD, circulatory problems, smoking
Sx: vertigo, dizziness, dysarthria, diplopia, numbness
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Labyrinthitis
- Causes: Viral illness (MOST COMMON), but can be caused by trauma, bacterial infection, allergies, benign tumor and certain medicatoins.
- Sx: vertigo, tinnitus, nausea, loss of balance
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Vestibular schwannoma:
Sx: unilateral sensorineural hearing loss, sometimes imbalance and tinnitus but symptoms are persistent and progressive
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Meniere disease
- Cause: increased volume and/or pressure of endolymph
- Sx: Episodes lasting 20min-24hrs, vertigo, hearing loss, tinnitus and/or aural fullness
- Dx: Audiogram, MRi to r/o central cause of vertigo
- Tx: Diet and lifestyle, Meds (hydrochlorothiazide, betahistine)
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Vestibular neuritis:
- Cause: inflammatory disorder affecting the vestibular branch of the 8th cranial nerve 2/2 viral infection.
- Sx: rapid onset, N/V, gait impairment. resolved within days.
PTH and Ca
hypocalcemia
Ca correction with albumin
PTH:
Kidney: increased calcium reabsorption and phosphate excretion
Bone: Ca release
Increases Vit D –> absorb Ca and phosphate from gut
Primary hyperparathyroidism:
- High PTH, High Ca, Low Phos
- High Ca: Stones (renal), bones (pain), groans (abdominal pain), thrones (increased urinary frequency), psychiatric overtones (anxiety, altered mental status)
Hypoparathyroidism:
- sx: Asx, perioral or peripheral numbness/tingling, muscle cramps, carpel spasm (Trousseau sign) & facial twitch (Chvostek sign), prolonged CT, tetany, seizures
- Low PTH, Low Ca, High Phos
Pseudohypoparathyroidism
- End organ resistance to PTH –>
- High PTH, Low Ca, High Phos
Vit D deficiency:
High PTH, Low Ca and Phos
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Calcium correction equation
Calcium homeostasis involves blood transport as albumin-bound calcium (45%), ionized calcium (40%) and calcium bound to inorganic and organic anions (15%)
Corrected Ca = measured Ca + .8*(4 - measured albumin)
Hyperthyroidism
Tx (1st then 2nd)
Thyroid hormones cause an increase in sympathetic activity d/t increased responsiveness to catecholamines.
Dx: TSH
Tx:
1st: Beta-blockers: help with hyperadrenergic symptoms and control HR.
2nd: Propylthiouracil (PTU) , Methimazole but can take several weeks
3rd: radioiodine ablation, or thyroidectomy
Subacute thyroiditis
Sx, Labs, Uptake, Path, Tx
- Preceded by viral illness
- Painful
- Transient hyperthyroid sx d/t release thyroid hormones
- High ESR & CRP
- Decreased Radioiodine uptake (not making new T3/T4)
- Inflammatory infiltrate with macrophages & giant cells
- Tx: NSAIDs, beta-blockers, steroids if refractory. Methimazole is not effective
Hashimoto
Sx, Labs, Uptake, Histo, Comp
When to treat hypothyroidism
Conditions requiring high dose of thyroid hormone
- Anti- TPO (thyroid peroxidase) and antithyroglobulin antibodies
- Painless, Mainly hypothyroid sx
- Variable radioiodine uptake
- Hurthle cells (Eosinophilic epithelial cells)
- Comp: Thyroid lymphoma
Hypothyroidism does not require tx unless:
1. Antithyroid antibodies
2. Abnormal lipid panel
3. Sx of hypothyroidism
4. Ovulatory and menstrual dysfunction
Conditions requiring higher dose of levothyroxine
should be taken on an empty stomach with water at least 30-60min before breakfast.
-Malabsorption (celiac disease)
- Drugs that interfere with absorption (iron, calcium) , separate by 3-4hrs
- Drugs that increase thyroxine metabolism (phenytoin, carbamazepine, rifampin)
- Others: obesity, pregnancy, overt proteinuria
Prolactinoma
Pathophysiology, Sx, Tx
High prolactin –> suppress GnRH, LH, FSH, estradiol
Oligo/amenorrhea, infertility, galactorrhea, hot flashes, decreased bone density
Tx: Dopamine agonist (cabergoline, bromocriptine), transsphenoidal surgery
Cerebral venous thrombosis vs arterial thrombosis
Presentation, Dx, Tx
Venous thrombus –> impaired CSF absorption –> Headache, increased ICP, papilledema –> hemorrhage –> seizures
Encephalopathy
Arterial: slurred speech, weakness
Dx: CT –> MRV
Tx: LMWH