Showing posts with label medication. Show all posts
Showing posts with label medication. Show all posts

Why Prescribe Single Pill Combinations? (Toub, 10/14/2026)

A recording of this presentation is available HERE.

Thanks so much to Dr. Danny Toub, core faculty, family doctor, and HIV specialist, who gave an awesome talk on Single Pill Combinations (SPCs). The recorded talk is available above. Dr. Toub started off by saying he wasn't going to talk about HIV meds-- and he didn't!-- instead he gave a convincing argument why we should DEFINITELY be considering SPCs for patients with hypertension, at the very least.

Single Pill Combinations (SPCs) or Single Tablet Regimens (STRs) or Fixed Dose Combinations (FDC) are, by definition, medications that contain two or more more pharmaceutical ingredients within a specified ratio, combined in one form, in the form of a tablet, capsule or injection. SPCs go way back to the 1950s (hydralazine and reserpine) and 1960s (birth control pills-- estrogen and progesterone).

There are a fair number of SPCs on the Medi-Cal formulary (see image):

including a fair number of medications to treat/prevent infectious disease (see image):

SPCs have many advantages, including 1) prevention development of drug resistance (e.g. h pylori regimens) 2) improved efficacy 3) improved adherence (only 50% of patients take medications as prescribed) in addition to 4) fewer pills, 5) less frequent dosing. Some SPCs can even deter misuse (think of Suboxone, which contains both naloxone and buprenorphine).

AND, as Dr. Toub pointed out, another advantage is SYNERGY-- that is, the unified whole is even better than the sum of all the parts. 

With specific regard to hypertension, we know that only 25% of US adults with hypertension are at goal BP, less than half of patients with hypertension who are on meds are at goal, about 40% of US adults with hypertension are still only on a single medication, whereas about 75% of patients NEED a second agent to achieve BP control <140/90.

The AHA released a 2026 statement on the use of SPCs for hypertension, specifically: saying that the use of SPCs is preferred OVER stepped care (i.e. stop adding one med at a time, start out with two!)
https://www.ahajournals.org/doi/epub/10.1161/HYP.0000000000000258

The table below comes from a 2025 Lancet article summarizing how much each single agent decreases blood pressure:

https://pubmed.ncbi.nlm.nih.gov/40885583/

A 2009 Meta-analysis from the American Journal of Medicine, with over 11,000 patients combining 42 trials, found that adding a second agent had 5x the blood pressure effect as doubling the first agent!! It appears that the greatest bang for your buck (i.e. the most potent BP effect) comes from combing calcium channel blockers (CCBs) and angiotensin receptor blockers (ARBs). This combo reduced systolic BP by 19mmHg
AND, it gets even better: combining meds into a SPCs ironically seems to result in fewer adverse effects. For example, monotherapy with CCB is known to cause peripheral edema, but combining with an ARB seems to offset that side effect. In fact, in another Metanalysis from JAMA published in May 2026, the combination of CCB+ARB had the best profile, but even a triple combo (ARB/TZ/CCB) had better side effect profile than placebo. 
While some SPCs (especially newer branded ones) wind up being more costly, some actually cost less than the combination of separate medications. 

Santa Rosa Community Health (SRCH) has a Hypertension Guidelines that are taken from the Kaiser Hypertension Guidelines, generally using SPC that contains HCTZ+ lisinopril. Goal is to minimize pill burden AND get BP under control quickly with more convenience and less copays.

To be clear, SPCs are not without some disadvantages. They can be more costly. Some are gimmicks by pharma to sell "new drugs" with new names. Some combinations contain more medications than a patient actually needs (have you ever seen that cream from Mexico that combines topical steroid with anti-fungal AND anti-bacterial cream?). They can feel inflexible, lead to adverse effects and/or drug-drug interactions, and it can create a situation when a patient does have a side effect where it is very difficult to determine which agent is the culprit.

***
What about for other conditions?
Dr. Toub was also encouraging us to consider SPCs for Cardiovascular Kidney Metabolic Syndrome (CKM). There are multiple SCPs that target these diseases (see image) and considering the number of medications and risks of morbidity/mortality, it is reasonable to think about pill burden at the very least. While there are no studies yet confirming improved outcomes with SCPs for CKM, initial combo treatment may be considered. 



In summary, SPCs are already widely accepted for many conditions, multiple guidelines recommend SCPs for Hypertension management, and they likely lead to better adherence, safer, more effective, and yet still under-used. Get to know your Medi-Cal formulary SCPs and go out and heal!











Migraine: physiology, new medications, and integrated approaches to management (Dacre, 1/14/2026)

A recording of this presentation is available HERE.

Many thanks to Dr. Mike Dacre for a presentation this week on Migraines. 

My notes:

Migraine syndrome is super common (~10% of all people), 1 billion people globally, 2nd cause of disability worldwide, 50% underdiagnosed and undertreated. 2:1 female to male ratio

  • Migraine headaches 4-72 hours
  • Note Pediatric usually max 2-4 hours (often not unilateral)
  • Classic pattern of prodrome>> aura>> headache>> postdrome


What causes migraine? Has long been thought of as a blood vessel problem (spasm vs dilation)>> pain often pulsatile, worse with movement/position changes, vasoconstrictors (caffeine, ergo alkaloids) then migraines get better, vasodilators (Viagra) make migraines worse. 

BUT this understanding is now known to not be true. In actuality, the blood vessel changes are SECONDARY. Now belief is that migraine is primarily a disease of neuronal activity: large ion shifts (potassium, glutamate, ATP across cell membranes)>> two receptors particularly notable now, include CGRP receptor and PACAP

  • CGRP is potent vasodilator, but is a side effect of activation of this cascade>> mast cell degranulation, inflammation and sensitization
  • get irritation and inflammation around the blood vessels, causing painful vasodilation


Migraines tend to start in the brainstem (where trigeminal nerve originates), direction impacts the type of migraine a person experiences. Where it moves, impacts the symptoms/manifestations


I love this simple diagram of how genetic set point+ cumulative burden push people toward migraine thresholds and lead to migraine syndromes:


Migraine headaches can move from being episodic to being chronic/intractable. Once you get migraines frequently enough, you can get medication overuse headaches, which then push you to central sensitization, which makes you more likely to get migraines. Similar to chronic pain syndrome progression>> it is not uncommon for people with headache syndromes to not seek care, overtake meds, and then have their disease progress to central sensitization and "chronification".

Abortive Treatments

Medications 

    • NSAIDs are very effective (shouldn't be taken more than QOD due to risk of medication overuse headache)
    • acetaminophen and caffeine can potentiate/help (care with overuse)
    • Excedrin is "worse" for medication overuse (no more than 5 times/month)
  • Corticosteroids + PPI
    • short course of prednisone has good evidence (NNT 9)
  • Triptans (actually inhibit CGRP release)
    • should be used in episodic migraine, more effective when done before pain starts (aura phase), not useful after 1 hour after onset of pain
    • NNT 4-5
    • Sumatriptan and Rizatriptan are most commonly used (familiarity)> no head to head trials
  • Care with vasoconstriction effect (e.g. contraindicated in CAD, uncontrolled Htn)

  • Opioids don't work well, high risk for misuse/dependence
  • Caffeine is very effective in some people for aborting migraine, but people with > 2 cups coffee/day have more frequent and worse migraines
  • Ditans: not available in US (schedule 5) but do see them in Middle East and Latin America
Nerve Blocks
Greater occipital nerve block>> safe and effective even in people who don't have predominant occipital pain, helps to abort migraine. 
  • can be done with or without ultrasound
  • Can do block + anti-emetic + steroid
  • lidocaine+ bupivacaine
  • very safe (low vascular, infection risk)

Preventive Treatments

Medications
  • Beta blockers all work (propranolol, metoprolol)
  • TCA: Amitriptyline
  • SNRIs
  • ARBs
  • Anti-seizure meds (e.g. valproate, topiramate)>> best responders are people who failed other classes
  • Anti-CGRPs: American Headache Society released guidelines in 2024 that these meds are first line for anyone with migraine >15 days/month ($600-700/month)
    • safe and effective
    • can be prescribed by PCPs
    • can get covered by PHP (prior auth)
    • one comparison study vs. topiramate, better tolerated
  • Gepants
    • remigapant, ubrogopant (can be used for ppx and abortive)
  • Supplements
    • Magnesium 400mg/day (moderate evidence)
    • Riboflavin 400mg/day (good evidence)
    • Coq10 (not great evidence) 100 TID
  • Botox NNT 9 (50% reduction in HA days)
  • Acupuncture NNT 11 (weekly acupuncture, 50% reduction in HA days)
  • OMT/PT/massage are all also very effective, studies to support their use in reducing HA days

Summary:


Thyroid Hormonal Disease (Magnotti, 4/17/2024)

 A recording of this presentation is available HERE.

***

Thanks to Dr. Mike Magnotti, SMGR Endocrinologist, for an excellent presentation on Hypo and Hyperthyroid. This was a jam-packed presentation. Check out the link above or my notes below.

Hypothyroidism

Hypothyroidism is characterized by non-specific and relatively common constellation of symptoms, including fatigue, weight gain, mental cloudiness, cold intolerance, etc. Plenty of people with these symptoms believe they have thyroid disease (and will even feel better on thyroid replacement), but this doesn't mean they actually have thyroid disease. 

Of note, weight gain is a known symptom of hypothyroidism, but obesity is not generally caused by hypothyroidism. Treating a patient's hypothyroidism can help mood, mental acuity, and focus but likely little (if any) weight loss.

Also of note, alopecia 2/2 hypothyroid takes a very LONG time to get better -- 6 months to 1 year, even with normalization thyroid hormone. Patients need to either be patient or use another med (e.g. Rogaine) in the meantime.

The only test you need to diagnose hypothyroidism is TSH. A normal TSH range is 0.5 to about 5 and excludes thyroid disease (except in very rare cases). Always want to check twice (there are lots of transient highs that can self-resolve), on repeat TSH, also check FT4, consider thyroid antibodies (not recommended in guidelines). Ft4 distinguishes between subclinical and clinical hypothyroidism. Antibody results do NOT change treatment, but can be helpful to patients to know WHY they have hypothyroid. No need to monitor antibodies -- levels change due to immune system activity and do not indicate illness state. 

High TSH, low FT4--> overt hypothyroidism, treat with levothyroxine

High TSH, normal FT4--> subclinical hypothyroidism, consider treatment**

If thyroid antibodies are elevated, dx is most likely Hashimoto's thyroiditis

TSH increases with age. A TSH of 6-8 may be normal in patients >70 years old; TSH can also be low in younger people (0.3-0.5 can be normal in young).

**Treat patients with subclinical hypothyroidism if they have symptoms, if TSH>10 (even no symptoms because of reduced risk CAD), TSH 7-10 if under 65. Only treat elderly patient <7 if you really believe they are symptomatic. 

Note: Biotin supplements alter the ability of the assay to detect thyroid hormones (it doesn't change actual thyroid hormone). Must be high dose biotin-- e.g. those in hair and nail formulations. Should avoid products with biotin 3 days before the assay. Biotin generally makes people look hyperthyroid (Low TSH, high FT4)

Treatment of hypothyroidism

Treatment of hypothyroidism is Levothyroxine (T4)

1.6 mcg/kg/day is the FULL replacement dose of thyroid hormone (patients with NO thyroid will need this full dose)

    • If older patient, start slow to avoid cardiac issues, arrhythmia
    • Younger person with a very HIGH TSH probably needs most of the high replacement dose right up front. If they have a lower TSH, can start with 1/2 the dose
  • take 30 minutes before food, 4 hours before calcium/iron/vitamin (absorption). 
  • brand does NOT matter unless someone has intolerance to fillers/dyes in a certain brand
    • Tirosint brand is a gel cap formulation with no filler, also liquid version, theoretically has least likelihood of having adverse reaction, but very expensive
    • For rare patients who are super sensitive to batch variations, use the same brand to maintain consistent
  • Only use TSH to monitor (goal is anywhere in the normal range), titrate to patient's feeling about how they feel
    • no need to monitor T3 levels, which vary more with stress and illness (helpful in hyperthyroidism)
  • Never use T3 alone! Our system has no way to regulate T3 levels in our body. T3 is the more active form. There is internal regulation of conversion T4>T3 (e.g. hospitalized patients have inhibition of conversion, normal stress response), but T3 is unregulated.
T3/T4 combination not generally recommended as first line treatment because most people feel fine on T4 alone. T3 is converted to T4 via deiiodinase. There are some (rare) patients with reduced ability to convert T4 to T3 (no ability is not compatible with life). Most people feel better on T3 because it gives them more energy. T3 makes people feel better like caffeine makes people feel better. 
  • Most trials adding T3 to T4 show no benefit, though a few studies show some benefit. Hard to quantify symptoms energy, focus, sleep. Some people feel a rush when they take T3. 
  • Consider adding T3 if patients are not better on T4 (but not an excessive amount)
  • T3 has a very short half-life (needs to be taken am/pm, e.g. 7am, 3pm)
  • Armour thyroid formulation (pig and cow thyroid) contains more T3 than normal human (4:1 ratio T4:T3 in Armour, humans generally have T4: T3, 13-16:1)
    • if you check T3 levels, you will see relatively high T3, low T4 and normal TSH
    • more variability from batch to batch (higher risk over-replacement)
    • Dr. Magnotti generally does not recommend Armour, unless a patient is stable on it and you are just continuing it
  • If you want to give T3, should dose separately
    • T4 is 4x potent as T3
    • Goal is maintain ratio T4/T3 13-16:1, e.g. 5mcg T3, 75mcg T4
    • T3 only comes as 5mcg and 25 mcg. Generally don't use 25mcg pills
  • Do NOT use T3 in pregnancy (doesn't cross placenta, so mom can be euthyroid and baby can be hypothyroid)
  • Only monitor via TSH, symptoms
Secondary hypothyroidism is VERY rare. Unlikely to be de novo or surprising diagnosis. Patients with known pituitary tumor, history of pituitary or sella radiation, other pituitary hormone deficits (prolactin, LH, FSH). In these rare patients, TSH is useless. You treat using FT4 to monitor, goal mid normal.

Hypothyroid in pregnancy
  • As soon as woman is pregnant, increase the dose up front 20-30% (right away) because risk of hypothyroidism on the fetus is WAY higher than hyperthyroidism 
  • Check TSH q4 weeks (up through the second trimester)
  • No T3 alone in pregnancy 
  • Current goal in pregnancy is TSH<2.5
  • Immediately after delivery, back to usual delivery
  • Recheck TSH 8-12 weeks post partum (not too soon) because lots of women have post partum thyroiditis, which can confuse things and make you worried they have levothyroxine too high
  • Let patient symptom guide 
If patient diagnosed with hypothyroidism during pregnancy. Guidelines vary about screening. 
BUT . . .
If TSH>4, treat
If TSH <2.5, no treatment
If between 2.5-4, check TPO, especially if recurrent miscarriage.
Starting dose based on level of TSH. If above 15-20, be more aggressive
Recheck 4 weeks even though not fully equilibrated.

***
Hyperthyroidism can definitely be more complex than hypothyroidism; there are more causes to consider, and the treatment is more nuanced.

Best first test for hyperthyroidism is TSH.
  • If TSH is LOW, check BOTH FT4 and FT3 (elevations in either can cause overt disease),
    • Also check TSI and/or TRAB (same test, different assay). 
    • If Ab positive, your patient almost certainly has Grave's disease.
  • If TSH is LOW, but BOTH FT4 and FT3 are normal>> this is by definition, subclinical hyperthyroid. 
    • Treat subclinical hyperthyroidism if TSH<0.1 (or <0.3 if older, atrial fibrillation).
    • CV risks of hyperthyroidism are definitely increased when TSH<0.1.
  • If TSH is NORMAL with elevations in FT4 or FT3, this either secondary hyperthyroidism (VERY very very rare) OR T4 resistance (genetic)
    • Refer to endocrine.
Additional lab findings: isolated elevation in alk phos is common with significant hyperthyroidism, will go down when treated. Transaminitis can be caused by methimazole but sometimes is also seen in hyperthyroidism.

Causes of hyperthyroidism
Grave's disease is by far the main cause of hyperthyroidism (75-80%, especially in younger patients), toxic multinodular goiter relatively more common in older population, also single functional nodule. Knowing the cause of hyperthyroidism doesn't impact who needs to be treated but can influence treatment decisions. 
  • +TSI and no palpable nodules on exam (usually sizeable on exam, 2-4 cm) >> patient almost certainly has Grave's disease (no scan needed)
  • -TSI and/or no nodules on exam >> need uptake scan (to r/o functional nodule)
  • If palpable nodule>> need both ultrasound and uptake scan
    • Toxic multinodular goiter usually is HUGE, nodular on exam

NOTE: If TSH is NOT close zero, the radioactive uptake scan is not reliable (even at 0.2 or 0.3, scan will generally be normal). If you cannot get uptake scan, ultrasound can be helpful (even without nodules). they evaluate blood flow. If blood flow is low, likely thyroiditis. High blood flow, likely Grave's. 

If no uptake>> likely dx thyroiditis (unless people taking iodine supplements, kelp, seaweed, or recent contrast in last 3 months. Amiodarone can also cause no uptake, even 3 months after taking it.
If normal or increased uptake>> dx Grave's
If uptake in single nodule>> dx toxic solitary nodule
Patchy uptake all around >> toxic multinodular goiter

Treatment of hyperthyroidism
3 options: methimazole, iodine (I-131), thyroidectomy. Beta blocker for symptom management

Methimazole is first line for most causes. 

Methimazole 10 mg/day, 20 mg/day, 40 mg/day for mild (<2x ULN), mod (2x ULN), severe (>2x ULN) disease, respectively. Taper down to 5-15mg (usual maintenance dose). Leave people on methimazole for 1-2 years before stopping. Want to be sure to have negative TSI (antibody) if they have positive to begin with. Don't stop methimazole in anyone who still has antibody at the receptor (+TSI is causing the hyperthyroidism).

There are some exceptions.
  • Iodine should be considered for young women who desire pregnancy and people without eye disease
    • Younger women who desire pregnancy may benefit from treatment with iodine treatment because methimazole can take years to get into remission. 
    • Can get pregnant 6-9 months, need normal TSH (with levothyroxine). 
    • Even after 3-4 years, with methimazole may not be in remission. Delays childbearing.
  • Iodine is also great for single toxic nodule because people will come out euthyroid. Likely curative. Normal gland not affected. 
  • Very severe hyperthyroidism in a younger person, especially with a large gland, they are very unlikely to have long-term remission at all with methimazole. Consider iodine vs. surgery.
  • Surgery may be best option if need to get thyroid hormone levels down quickly. It will still take weeks (body has to metabolize FT4 already floating around)
    • Consider surgery in case of: 1) very large goiter,  2) need for rapid correction, 3) concern for malignancy, 4) combo hyperthyroid+ hyperparathyroidism
Hyperthyroid eye disease: Send to neuro-ophtho if thyroid eye disease. Iodine can worsen thyroid eye disease. (if mild, can do Iodine with 3-4 months of prednisone to protect against progression). 

Hyperthyroid in pregnancy: 
Do NOT treat subclinical disease. 
Use PTU in first trimester, change to methimazole in 2nd and 3rd trimesters.
Target Total T4 and Total T3 in the high normal range, which is 1.5x ULN for pregnancy range due to higher estrogen, binding globulin. 

Why Prescribe Single Pill Combinations? (Toub, 10/14/2026)

A recording of this presentation is available  HERE . Thanks so much to Dr. Danny Toub, core faculty, family doctor, and HIV specialist, who...