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Yale 20: Non-Opioid Pain Management

June 12, 2024
ID
11778

Transcript

  • 00:00Hi everyone, my name is Julia Joseph.
  • 00:04I'm a current third year internal medicine
  • 00:06resident at Yale New Haven Hospital.
  • 00:08I created this video with the help
  • 00:09of our palliative faculty member,
  • 00:11Doctor Persik in order to
  • 00:13discuss non opioid pain options,
  • 00:15especially from an inpatient perspective.
  • 00:17I remember being an intern,
  • 00:19especially on nights, and not having
  • 00:21an idea of what the options were to
  • 00:23treat pain before reaching for opioids.
  • 00:25So hopefully this will
  • 00:27help build a framework.
  • 00:29We will first start with a case,
  • 00:31then go over basic principles,
  • 00:33dive into the non opioid pain options before
  • 00:37concluding with our case and learning points.
  • 00:39So we'll start off with a familiar situation.
  • 00:42Imagine you're the overnight intern
  • 00:44and you get woken up with a page.
  • 00:46Hey doc patient in room 5 two
  • 00:48O 8 is having a lot of pain.
  • 00:50Can you give him something?
  • 00:52What do you do?
  • 00:55One acronym that can be helpful
  • 00:57to assess pain is OPQRST,
  • 00:59which many of you may have
  • 01:01been taught in medical school.
  • 01:03It will remind you to ask about the onset,
  • 01:05the provoking factors,
  • 01:07the quality of the pain,
  • 01:09whether the pain radiates anywhere,
  • 01:11the severity of the pain,
  • 01:13and the timing and duration of the pain.
  • 01:19As you gather this information,
  • 01:21it's helpful to classify the type of pain.
  • 01:23There are several types of pain syndromes,
  • 01:26but I've included three major types
  • 01:28of syndromes that you may encounter.
  • 01:30No sceptive pain is pain that arises
  • 01:32from the activation of no sceptors due
  • 01:35to a pain impulse that was detected
  • 01:37as demonstrated here. For example,
  • 01:39when you stick your hand on a nail,
  • 01:41the no sceptors transduce the
  • 01:43signal back to your brain which
  • 01:45registers the painful impulse.
  • 01:47Neuropathic pain is actual damage to
  • 01:50the somatosensory nervous system.
  • 01:51You will commonly see this in patients
  • 01:53with long standing diabetes and have
  • 01:55sustained nerve damage in their feet,
  • 01:57for example.
  • 01:58Finally, nosey plastic pain arises
  • 02:01from altered perception of pain.
  • 02:03While there's no evidence of tissue damage
  • 02:05as you might see a nociceptive pain,
  • 02:07they are experiencing pain from
  • 02:10dysregulated sensory processing.
  • 02:12You may see this in conditions
  • 02:15like fibromyalgia.
  • 02:16All right, so let's dive into
  • 02:18our non opioid pain modalities.
  • 02:21So the first medication we'll
  • 02:23discuss is acetaminophen.
  • 02:24Acetaminophen is very effective
  • 02:26for mild to moderate pain,
  • 02:28but can also help with severe
  • 02:30pain when combined with opioids.
  • 02:31It works by inhibiting prostaglandins,
  • 02:34which decreases pain signaling
  • 02:36and tamps down fevers.
  • 02:37IV Tylenol has the same efficacy
  • 02:39as rectal and oral Tylenol,
  • 02:41but works quicker.
  • 02:42It can be hard to get approved
  • 02:44though because of the higher cost.
  • 02:46Rectal and IV administration can
  • 02:48especially be useful for patients
  • 02:51at end of life or patients who
  • 02:53can't take oral Tylenol safely.
  • 02:54The absolute Max that's recommended
  • 02:57is 4G a day,
  • 02:58but for those patients who have a history
  • 03:01of cirrhosis or chronically used Tylenol,
  • 03:03you should really consider a reduced
  • 03:06maximum of two to three grams per day.
  • 03:10You should be careful when keeping
  • 03:12a patient on scheduled acetaminophen
  • 03:14when you want to avoid masking fevers,
  • 03:16such as when you are taking
  • 03:18care of neutropenic patients.
  • 03:19You should also be careful prescribing
  • 03:21too much acetaminophen and patients
  • 03:23who are at risk of accumulating
  • 03:26the toxic metabolite nap Qi.
  • 03:27These include patients with low glutathione
  • 03:30stores like malnourished patients,
  • 03:32patients with ongoing alcohol use,
  • 03:35or patients who are on medications
  • 03:37that are CYP 450 inducers.
  • 03:41Acetaminophen,
  • 03:42as you can see here, gets metabolized
  • 03:44to nap Qi by the CYP 450 enzyme.
  • 03:47So you can imagine that if you
  • 03:49have medications that Rev up the
  • 03:51activity of the CYP 450 enzyme,
  • 03:53you will then accumulate more nap Qi.
  • 03:56You also need glutathione in
  • 03:59order to inactivate nap Qi.
  • 04:00So in patients who are malnourished
  • 04:02or don't have enough glutathione
  • 04:04stores you can imagine then you will
  • 04:06have more accumulated nap Qi that
  • 04:08will lead to toxic liver damage.
  • 04:12ENASAS are the next class of medications
  • 04:15which have anti-inflammatory
  • 04:16properties unlike acetaminophen.
  • 04:18They work by inhibiting Cox enzymes in both
  • 04:21the peripheral and central nervous system.
  • 04:23Toradol is an example of a non selective
  • 04:26NSAID while selecoxib is a Cox two
  • 04:29selective NSAID by inhibiting Cox two.
  • 04:31Selecoxib confers a degree of
  • 04:35gastric protection by only
  • 04:38working on the Cox 2 enzyme.
  • 04:41Unfortunately,
  • 04:41NSAID's overall have an increased risk of
  • 04:44MIS and strokes as well as risk of AKI.
  • 04:47The risk of AKI is particularly
  • 04:49high in the 1st 30 days.
  • 04:51Cox two inhibitors do have more GI
  • 04:54protective effects but unfortunately still
  • 04:55have the other serious side effects noted.
  • 04:58In general,
  • 04:58you should avoid in patients who
  • 05:00are at risk of bleed,
  • 05:01significant cardiac history or
  • 05:03renal impairment.
  • 05:07This is an NSAID reference table that you
  • 05:09can pause if you'd like to learn more.
  • 05:11The ones pointed out are some
  • 05:12common NSAID that you may come
  • 05:14across such as Motrin and Toradol,
  • 05:16which you could see in the hospital,
  • 05:17especially Toradol because it's
  • 05:19a non selective NSAID that comes
  • 05:21in IV or IM formulation. There's
  • 05:23Meloxicam which is a relatively
  • 05:25Cox two selective NSAID,
  • 05:27although it has some Cox one activity.
  • 05:29And then there's Sela Coxib which
  • 05:31is a Cox two selective NSAID.
  • 05:33Next, let's talk about some topical options.
  • 05:36Diclofenac is a topical NSAID that
  • 05:38can be used up to four times a day.
  • 05:40You can use 2G for each upper extremity
  • 05:42joint and 4G for each lower extremity joint.
  • 05:45You should not use more
  • 05:46than 32 grams in one day.
  • 05:48The systemic exposure from gel form
  • 05:50is on average 6% of the oral form.
  • 05:53It carries the same risk profiles oral
  • 05:55NSAID's, but it overall is better tolerated.
  • 05:58Capsaicin cream is derived from
  • 05:59Hot Chili Peppers and works by
  • 06:01desensitizing no seceptive fibers.
  • 06:03It can also be useful in neuropathic pain.
  • 06:05You can dose up to four times a day,
  • 06:07but it may take several weeks
  • 06:08before you see an effect.
  • 06:10Stinging and burning at the site of
  • 06:12application has also been reported.
  • 06:14Finally, lidocaine is an anaesthetic
  • 06:16agent that comes in several forms.
  • 06:18You can dose 3 patches of 5% lidocaine
  • 06:21in one setting with a 12 hour on
  • 06:23period and 12 hour off period.
  • 06:25Systemic exposure is approximately
  • 06:27less than 5% with this regimen,
  • 06:29so systemic side effects are
  • 06:31overall relatively rare.
  • 06:34Gabapentinoids are the next class of
  • 06:36medications that we'll talk about.
  • 06:38They were initially developed as
  • 06:40anti seizure agents because they
  • 06:41suppress neuronal excitability by
  • 06:43working on voltage gated calcium
  • 06:45channels as shown in this diagram.
  • 06:47They can also be used to
  • 06:50treat neuropathic pain.
  • 06:51These are both commonly used gabapentinoids.
  • 06:54Pregabalin is more potent and more
  • 06:57predictably absorbed than gabapentin.
  • 06:59Peak blood concentration occurs
  • 07:01within an hour of taking pregabalin,
  • 07:03but can take approximately
  • 07:053 hours with gabapentin.
  • 07:07Due to being a scheduled
  • 07:09class 5 controlled substance,
  • 07:10Pregabalin is not as easy to
  • 07:14prescribe as gabapentin.
  • 07:15When prescribing pregabalin,
  • 07:16you can start at 50 to 150 milligrams a day,
  • 07:20usually in two to three divided doses.
  • 07:23From there,
  • 07:24you can up titrate every week
  • 07:25to a maximum of 300 to 600
  • 07:28milligrams per day in two to three
  • 07:30divided doses to reach effect.
  • 07:32With gabapentin,
  • 07:33you can start at 300 milligrams every day,
  • 07:36usually in three divided doses.
  • 07:38You can up titrate to a maximum of 3600
  • 07:42milligrams every day to reach effect
  • 07:46CNS. Depression is a common
  • 07:49problem with gabapentinoids,
  • 07:50especially when used alongside opioids.
  • 07:53Toxicity can especially be seen
  • 07:55in patients with renal impairment,
  • 07:57so be cautious in those with Akis or
  • 07:59history of CKD if stopped suddenly.
  • 08:02Withdrawal syndromes have been
  • 08:03described with gabapentinoids similar
  • 08:05to alcohol and benzo withdrawal,
  • 08:07including seizures.
  • 08:08So in admitting a patient on
  • 08:10high doses of these medications,
  • 08:12be careful not to stop them immediately
  • 08:15to avoid precipitating withdrawal,
  • 08:16which can occur within 12 hours to
  • 08:19seven days after discontinuing.
  • 08:22The last
  • 08:23non opioid medication we will discuss
  • 08:26is duloxetine, a type of SNRI.
  • 08:29Of all antidepressants,
  • 08:30duloxetine has the largest evidence
  • 08:32base to support its use in pain relief.
  • 08:35It has been FDA approved for several
  • 08:37types of pain syndromes but unfortunately
  • 08:39comes with several noted side effects.
  • 08:41As listed here.
  • 08:42You can start duloxetine at 20 to 30
  • 08:45milligrams a day for one week and then
  • 08:47from their up titrate until receiving
  • 08:49a maximum of 60 to 120 milligrams.
  • 08:51You should see pain improvement as early
  • 08:54as the first week of implementation.
  • 08:56You can especially consider SNR is
  • 08:58like duloxetine for those patients
  • 09:00who have comorbid depression and pain.
  • 09:05Easy measures that can be implemented
  • 09:07and that are often forgotten in the
  • 09:09inpatient setting include using heater ice,
  • 09:11physical therapy to help with mobility,
  • 09:14and using foam support or
  • 09:16pillows to help with elevation.
  • 09:18Now let's get back to our case.
  • 09:20You were the overnight intern
  • 09:22paged about a patient's pain.
  • 09:24You do a quick chart review and note
  • 09:26your patient has a history of type 2
  • 09:27diabetes and is on a blood thinner.
  • 09:29Their labs are otherwise unremarkable.
  • 09:32Your sign out says that he
  • 09:34responds to Oxy at bedside.
  • 09:35Your patient tells you that he is
  • 09:37having burning pain in his feet that
  • 09:39is making it hard for him to sleep.
  • 09:41He already received 650
  • 09:42milligrams of acetaminophen.
  • 09:44That didn't seem to help.
  • 09:46So what can you do?
  • 09:48You determine that this is a
  • 09:50neuropathic pain syndrome based
  • 09:51on the patient's description.
  • 09:52You can give additional acetaminophen
  • 09:55or trial topical agents,
  • 09:57but given that this is likely
  • 09:59underlying peripheral neuropathy,
  • 10:00you could consider trialing a low dose
  • 10:02gabapentinoid or switching to duloxetine,
  • 10:04especially if he's already on an SSRI.
  • 10:07In this case you should avoid ENSAES,
  • 10:09especially because he's on a blood
  • 10:11thinner and opioids would not be
  • 10:14first line in this pain syndrome.
  • 10:16So to summarize,
  • 10:17we discussed 3 pain syndromes
  • 10:20including nociceptive,
  • 10:21neuropathic and NOC plastic pain.
  • 10:24OPQRST is an approach to assess pain.
  • 10:27Acetaminophen should cautiously be used
  • 10:29in patients with low glutathione stores
  • 10:32and if they're taking CYP 450 inducers.
  • 10:36NSAID's can be non selective
  • 10:38or Cox two selective,
  • 10:39but overall their use can still be
  • 10:41limited by several side effects.
  • 10:43Topical options that we talked
  • 10:45through include diclofenac,
  • 10:46capsaicin and lidocaine.
  • 10:47Gabapentinoids including
  • 10:48pregabalin and gabapentin can
  • 10:51be useful for neuropathic pain,
  • 10:53and duloxetine is an SNRI that
  • 10:56also has pain relieving properties.
  • 10:59And if you're interested,
  • 11:00here are the many sources
  • 11:02that I used for this talk.