โค๏ธ๐ hi Sigal!
22.11.2024 19:01 โ ๐ 1 ๐ 0 ๐ฌ 0 ๐ 0@danbacic.bsky.social
Infectious Diseases at Montefiore ID. HIV, STIs, General ID, Med Ed, healthcare for all.
โค๏ธ๐ hi Sigal!
22.11.2024 19:01 โ ๐ 1 ๐ 0 ๐ฌ 0 ๐ 0Soft Smile Professional Headshot Wearing a Suit
Big Smile Professional Headshot Wearing a Suit
New headshot โจ๐ฅ๐ธ
Soft smile or big smile?
(Thanks to the hospital photographer for the pictures!)
If pts are down to do it, I give them multiple vaccines at once. Today a pt received six shots in the appt!
My thinking is that 1) we donโt know when/if their next contact with the HC system will happen, therefore will take the opportunity & vax 2) shortens time to complete series and protection
For those taking the ID Boards today:
When in doubt, the correct answer is always syphilis!
It is terrible that the US has had so many cases of congenital syphilis. More testing, treatment, and equitable prevention needed!
12.11.2024 22:50 โ ๐ 2 ๐ 0 ๐ฌ 0 ๐ 0Good luck everyone who is taking the Infectious Diseases Board examination tomorrow (myself included!)
๐๐ค
My prior and current institution very rarely use it, so wondering what colleaguesโ experiences with it are.
12.11.2024 06:06 โ ๐ 0 ๐ 0 ๐ฌ 0 ๐ 0Iโve used for a tx pt w/ simultaneous disseminated Nocardia & CRE Pneumonia & was like โoh! thatโs what itโs for!โ ๐คฃ
Iโve thought of some scenarios:
- MDR PsA R to CAZ-AVI & TOL-TAZ
- Polymicrobial infx w/ MDR PsA and CRE, especially if requiring anaerobic & some E faecalis coverage?
Others?
Asking my Stewardship & Micro colleagues
What are some use cases of IMI-REL?
It seems that situations in which it is distinctly superior or provides a unique advantage over alternatives are pretty niche.
(1/2)
I was not aware of NSV mechanisms until attending a lecture on the subject by Jonathan Li, who is a reservoir expert.
Iโve referred a couple of pts to his lab, but access to ultra-sensitive viral characterization is difficult outside major academic research centers.
www.nature.com/articles/s41...
Thank you for the articles, Sรฉbastian! Very interesting patients!
I feel like we need to increase awareness of this phenomenon amongst clinicians - because itโs actually not THAT uncommon, & it causes a lot of โfire drillsโ w/ changes in ART, multiple repeat tests & distrustโฆ (1/2)
I love you @sanfordguide.bsky.social !
You help me do me job better every day! โค๏ธ๐
Hopeful I can just abandon X soon and not have to cross post!
11.11.2024 23:24 โ ๐ 1 ๐ 0 ๐ฌ 1 ๐ 0What other common scenarios come up in your practice? Feel free to add, correct & comment!
11.11.2024 06:47 โ ๐ 1 ๐ 1 ๐ฌ 0 ๐ 0And finally, the amazing ART chart created by @serotavirus.bsky.social
drive.google.com/file/d/1Bfsq...
Useful resources for ART Management:
- Stanford Drug Resistance Database - hivdb.stanford.edu
- HIVassist.com
- IAS-USA - www.iasusa.org/wp-content/u...
- Liverpool HIV Drug Interactions Checker - www.hiv-druginteractions.org/checker
- Crushing & liquid ART: www.hivclinic.ca/main/drugs_e...
It ain't "broke," but you may as well "fix" it!
More about ART Switch, two-drug regimens, switching in VF, and other scenarios in our review article:
www.sciencedirect.com/science/arti...
And remember to also always incorporate:
- pt's preferences
- pill burden & size
- food requirements
- IM vs PO medication
- tolerability
- pregnancy
- toxicities
- DDIs
- caution if switching from a higher to a lower barrier to resistance regimen!
12) Efavirenz
Not very lipid friendly, has risk of DILI besides its well-established neuropsychiatric effects.
I have a low threshold to switch, especially if depression.
Watch for weight gain in people switching off EFV + TDF !
11) Abacavir
People on DTG/ABC/3TC come up once in a while. Long term use of ABC is associated with increased cardiovascular risk.
Would discuss switching with patient!
10) Older PIs
Numerous toxicities - switch!
The only PI we use in practice is darunavir - better tolerability & high barrier to resistance.
(Continuing atazanavir in pts who really don't want to switch & don't have kidney/GB stones or distressing jaundice might be reasonable)
9) AZT
Legacy un-switched AZT comes up once in a while due to a historical practice of using AZT in salvage regimens for people w/ K65R.
Outside perinatal HIV, hard to imagine a role for AZT nowadays w/ its BM & mitochondrial toxicities. There's better options - Switch!
8) A word about rilpivirine...
TAF/FTC/RPV came out in 2016 and became popular due to its small pill size. It's well-tolerated & safe, but check & inform:
-Needs full meal
-Cannot be given w/ PPIs
-Relatively low barrier to resistance, & if it develops, cannot use IM CAB/RPV
7) Persistent low level viremia (pLLV)
ART is often "intensified" in pLLV (eg, adding PI)
If non-adherence & resistance excluded & especially if pLLV is unchanged post switch, it may be due to factors that are not modifiable by ART (eg, clonal expansion of reservoir proviruses)
6) INSTI drug interactions
INSTIs are amazing, but there's a few DDIs. DTG increases metformin levels. Several anti-epileptics decrease INSTI levels!
The issue of pts on IM CAB (or PO INSTIs) who get phenobarbital for EtOH withdrawal sometimes comes up as well!
5) Older INSTIs
RAL & EVG/c have a lower barrier to resistance, and EVG needs Pk boosting (w/ its downsides). Pts w/ sub-optimal adherence, Pk issues, very high VL/low CD4, etc, can develop major INSTI mutations (eg, Q148H & N155H), w/ cross-resistance to CAB, BIC, & DTG.
4) Pts on DRV/b for unclear reasons
Great when well indicated, however, besides DDIs, there's cumulative metabolic (& other) risk.
Again, pause, review ART/genotypes, viremias & hx's of VF. Proviral "archived" genotypes can sometimes add a layer of info when unclear indication.
3) Pk boosters
Cobicistat/ritonavir may expose patients (esp if older w/ growing list of meds) to dangerous drug interactions by unaware providers - Cushing's from intra-articular steroids, amiodarone intoxication, bleeding w/ DOACs, etc.
Consider if PIs are really necessary!
2) Multi-pill regimens due to isolated NRTI resistance
Well >90% of pts w/ NRTI resistance (184V, K65R, TAMs, etc) can be suppressed w/ "recycled" NRTIs + fully active high-resistance barrier drug (BIC, DTG, or boosted PI)!
If adherent & suppressed, B/F/TAF is fine & VF rare!
1) Unnecessarily complicated multi-pill regimens
Pause, review ART history, cumulative genotypes, & think if a simpler regimen is possible/desired by the pt.
Calling Monogram might help recover lost genotypes.
HIVassist.com & StanfordDB are great resources!