This case describes a 63-year-old man, former narcotics officer, with a complex cardiac history who first presented 22 years ago after a suspected myocardial infarction (MI). He has a 21-pack year history of smoking, but stopped immediately after his MI. In 2009, the patient re-presented to cardiology and underwent a nuclear stress test demonstrating moderate ischemia in the anterior and anterolateral walls. A subsequent angiogram showed significant calcification in the left main coronary artery (LMCA) and the proximal left anterior descending artery (LAD). Disease in the right main coronary artery (RMCA) was also noted. He was referred for a 2D echocardiogram (ECHO) and recatheterization to explore the extent of his coronary artery disease (CAD; see supplemental Table 1, summary of cardiac history [2009–2010] and see supplemental Table 3, which illustrates both the single-photon emission computerized tomography and exercise tolerance test [ETT] findings [2010–2018]).

Stents were placed for diffuse atherosclerotic changes (see supplemental Table 1, summary of cardiac history [2009–2010]), and inoperable triple-vessel CAD which was identified via percutaneous transluminal coronary angioplasty. The RMCA was small, nondominant, with subtotal occlusion. There was 10% luminal compromise of the LMCA. Heavy calcification was noted within all of the diagonals of the LAD, whereas the LAD itself was diffusely diseased with areas of ectatic dilation and moderate stenosis, 60% to 70%. There was an aneurysmal dilation in the proximal LAD and a bare-metal stent was deployed distal to the dilation, in the mid-LAD. The left circumflex (LCX) was the dominant vessel and the AV segment was diffusely dilated and ectatic. The first and second obtuse marginal (OM1 and OM2) were 100% occluded and were noted to fill retrograde. A cutting balloon was unable to cross the area of disease in the both the OM1 and OM2. The obtuse marginal 3 (OM3) had multiple stenotic regions with the worst being 90% occluded and a bare-metal stent was deployed at the location of the near-total occlusion. The posterior descending artery was large and also diffusely atherosclerotic with multiple angiographic stenotic areas of varying severity; the worst located in the distal segments. During follow-up he reported little relief from the stent(s) and presented with angina for the first time.

An ECHO in March of 2010 showed a large wall-motion abnormality in the lateral and inferolateral walls. A low-normal left ventricular ejection fraction (LVEF), 40% to 50%, was also noted despite first-line mediations, which were modified for maximal impact and failing. Medications at that time where aspirin 325 mg, clopidogrel 75 mg, atorvastatin 40 mg, niacin 500 mg, omega-3, and carvedilol 3.125 mg (see table supplemental 2, for all medications and dosages [2009–2019]). The atorvastatin was subsequently terminated and rosuvastatin 20 mg was initiated, as was lisinopril 25 mg. The carvedilol was also increased to 6.25 mg (1.5 tabs, daily). These changes in his pharmacologic treatment produced significant results in his functional capacity, as demonstrated by his LVEF of 60% during a cardiac cath later in April 2010.

The patient underwent a cardiac recatheterization in April 2010 to visualize his coronary anatomy, assess the patency of the previous stents, and to place drug-eluting stents in other areas of significant disease, if necessary. The left heart catheterization demonstrated an RMCA with diffuse disease and total distal occlusion, LMCA with 40% occlusion, and an LCX with a fully occluded diagonal OM1 with a patent bare-metal stent in the proximal-OM3. The bare-metal stent in the mid-LAD was also patent. The LAD-1, however, was functionally occluded with poor run-off; it is noted that the vessel originally supplied a large area of myocardium. Drug-eluting stents were not placed, and the patient continued to report significant episodes of pain and discomfort consistent with stable angina.

In September 2010, he had his first ETT to assess performance and to quantify his ischemia (see supplemental Table 3, which illustrates both the single-photon emission computerized tomography and ETT findings [2010–2018]). The electrocardiogram (EKG) showed 2 mm ST depressions, exercise-induced premature ventricualar contractions, and the test was abandoned.

In 2011, the patient underwent a Single-photon emission computed tomography (SPECT) study. Using a modified Bruce protocol, he completed 2 minutes of stage III until he began to experience significant pain. The patient chose to continue the test using regadenoson to ensure complete vasodilation. The EKG showed diffuse 1.5 mm ST depression (see supplemental Table 3, which illustrates both the SPECT and ETT findings [2010–2018]). The ischemic changes first presented at the end of stage III of the modified Bruce protocol and were present up to 4 minutes in the recovery phase; they reversed to baseline after administration of aminophylline. Partial inferior wall scarring was noted; the LVEF was 54%. The Single-photon emission computed tomography ETT myocardial perfusion imaging study showed a mild intensity small-sized ischemic anterior wall defect extending from the mid to basal segments, a large size moderate intensity ischemic defect involving the anterolateral, inferolateral wall extending form the mid to the basal segments, and a small size mild to moderate intensity ischemic defect in the inferior wall. Compared to the prior test from 2010, the apical ischemia was no longer present, and the left ventricular wall hypokinesis was improved.

His medical records indicated persistent, recurring, chronic angina that would wax and wane in both severity and frequency, until progressing to unstable angina (UA) in 2012. As previously indicated, he has failed all first-and second-line pharmaceutical polypharmaceutical therapies. Most notably was the addition of ranolazine, which helped keep his chronic angina under moderate symptomatic control for several years. Ultimately, similar to other medications, ranolazine was modified for maximal impact and failed.

In late October of 2017, the patient sought evaluation for medicinal cannabis (MC). On initial visit, he presented with chronic chest pain due to UA that had not been totally relieved with long-term morphine treatment (morphine instant release [IR], 15 mg/8 h) and cardiac medications (rosuvastatin, amlodipine, clopidogrel, ranolazine, aspirin, carvedilol, lisinopril, and zolpidem; see table supplemental 2, for all medications and dosages [2009–2019]). His chest pain was 3/10 during evaluation but reported it may reach a level of 7/10 and would radiate to the left side of his chest. The patient says he was unable to walk long distances or perform mild/moderate physical activity. His symptoms were usually relieved by rest. He would, however, also experience frequent occurrences of angina unprovoked by physical activity or exertion, thus defining the presence of UA. He was started on MC at that time.

In late November 2017, the patient was seen for his first follow-up and presented with a decrease in the frequency of his chronic pain (CP). He stressed how the pain used to occur a few times/day and is now noticeably less often. He was also able to walk more than he previously was, but he still cannot do any strenuous activity. He was using a combination of high Δ⁹-tetrahydrocannabinol (THC) and low cannabidiol (CBD) strains (1:340 CBD:THC) (see table, supplemental 4, which displays the various medical cannabis strains used by our patient). It was discussed that he should be decarboxylating his MC and using it in edible form. The patient was able to reduce his morphine dosage from every 8 hours to once per day (q.d. morphine IR, 15 mg).

He returned in late December 2017 without any new significant relief compared to the previous month's progress. He would still get a feeling of tightness across his chest and need to sit down (q2/mo). It was recommended that he try a high CBD strain (1.2:1 CBD:THC) in combination with the previous THC strain via edible butter extraction bidaily (see table, supplemental 4, which displays the various medical cannabis strains used by our patient). Early February 2018, the patient reported that his pain was down from the old quality and character of sudden pain (even at rest), reported as a 6/10. Now described as a more consistent quality of dull pain rated at 3/10. He had been eating the recommended combo on toast 2 to 3 times/day (t.i.d.) and reports being happier during the day. He was still using morphine once daily (q.d. morphine IR, 15 mg). Overall, his chest discomfort and pressure were down 50%.

During his follow-up in the beginning of March 2018, he recounted now going days without pain. The patients’ CP was reduced from a few times a day to a few times a week but is dull and not sudden or debilitating like the past. It was discussed to stop the morphine if the MC is effectively controlling his CP. Later that week, the patient had a follow-up with his cardiologist, and they were both in agreement to continue using the MC if it is helping his UA and CAD symptoms, as well as reducing his dosage of morphine.

During his follow-up with cardiology, he was started on 2 new medications losartan and isosorbide mononitrate; the latter of which is known to mitigate reflex tachycardia and would be beneficial in a patient utilizing cannabis for congestive heart failure (CHF). It is also noted that he presented with edema but did not have jugular vein distention. He was referred for follow-up testing, and in April of 2018, the patient underwent another ETT (see supplemental Table 3, which illustrates both the SPECT and ETT findings [2010–2018]).

The EKG showed no evidence of exercise-induced arrhythmias (although a rare premature ventricualar contraction was present), and there were no signs of ischemia changes, a significant improvement (i.e., any ST changes were <1 mm and did not fulfill criteria for ischemia). Together, these findings mark improved functional capacity.

On his next primary care follow-up visit, in mid-May 2018, he had been off morphine for 6 days and controlling his symptoms using the recommended combo of high-dose CBD oil daily (t.d.) and THC butter 2 to 3 times daily (t.i.d.). He described the pain as no longer crippling and saw an increase in his daily functioning and overall activity, that is, he was able to walk more and perform more strenuous activity.

Early July 2018, he was completely off morphine (morphine IR, 15 mg/8 h) since April using the recommended combo of high-dose CBD oil and THC butter, as outlined above. His chest pain was significantly less frequent (2 times/day from >5 times/day before treatment) and less intense (now a dull pain and numbness that travels to the left arm and back, about 4/10). He reported that his last bad day was 6-weeks prior (mid-May 2018) and rated the pain on that occasion as a 9/10.

As of late March 2019, the patient reported only 2 episodes of chest pain since July 2018. The last one occurred in early March 2019 and was associated with a significantly emotional event. The patient is still opioid free, for 10 months, and uses a premixed combination of high-dose CBD hemp oil and a low dose of THC (15:1 CBD/THC) or the recommended extraction (1.2:1 CBD:THC), as outlined above. There have been no changes to his medications.