ACMT Toxicology Visual Pearl: Not Very A-peel-ing

Which of the following chemicals, commonly used in chemical peels, can cause severe, gray colored skin burns upon direct contact?
- Acetone
- Hydrogen peroxide
- Phenol
- Salicylic acid
[Author’s own image]

Which of the following chemicals, commonly used in chemical peels, can cause severe, gray colored skin burns upon direct contact?
[Author’s own image]

What commercially available product can cause blue-grey discoloration of the skin and conjunctiva with long term use?
[Image from Herbert L. Fred, MD and Hendrik A. van Dijk via Wikimedia Commons]

Improper preparation of this food causes poisoning from which toxic compound?
Image from Wikimedia Commons [1]

What medication given intravenously can cause the pictured finding?
Image from Dr. Fabio Corsi, MD [1]

Ondansetron is the most documented medication given in emergency departments (ED) throughout the United States [1]. We have all heard someone ask, “Can I get an order for 4 and 4 for this patient?” in reference to 4 mg of IV morphine and 4 mg of IV ondansetron. It has become common practice in many institutions to provide a prophylactic antiemetic prior to administering an IV opioid.
This dual therapy seems to make initial sense because all opioids carry a FDA warning that nausea may occur [2]. So why not administer an antiemetic to prevent it? Opioids cause nausea and vomiting due to its interaction on the chemoreceptor trigger zone (CTZ), increased vestibular sensitivity, and hindered gastric emptying [3]. The logic is to provide these patients with a 5-HT3 antagonist (i.e., ondansetron) to inhibit the opioid from exerting emetogenic properties on 5-HT3 receptors in the CTZ and prevent nausea and/or vomiting.
Multiple studies illustrate that morphine-induced nausea and vomiting is low, ranging from 2.0–20.2% in ED patients [4-9]. When discussing with ED nurses, nausea and vomiting are anecdotally associated with how quickly the IV opioid is administered and generally occurs within 5 minutes of administration.
So we should give IV ondansetron to prevent this, right? A common misconception with IV ondansetron is its onset of action. In fact, it can take anywhere between 27-34 minutes before there is a 50% decrease in nausea severity following the administration of ondansetron [10, 11]. This begs the question, does it really make sense to provide prophylactic antiemetics with IV opioids?
| Study | Intervention | Outcome | Conclusion |
|---|---|---|---|
| Bradshaw et al. [5] RCT- double blinded Performed in United Kingdom | IV morphine + placebo (n=136) IV morphine + metoclopramide 10 mg (n=123) | N/V between the 2 groups was not statistically significant (p=0.3). Overall incidence of N/V was low in both treatment groups (3.7% in placebo and 1.6% metoclopramide) | Pre-treating patients with metoclopramide was not necessary. Overall N/V associated with IV morphine was very low and recommended using antiemetics for patients who develop N/V. |
| Bhowmik et al. [8] RCT, double blinded Performed in India | IV morphine + placebo (n=53) IV morphine + promethazine (n=54) IV morphine + ramosetron (n=54) IV morphine + metoclopramide (n=54) | Overall incidence of N/V was low in all treatment groups (9.4% ramosetron, 18.5% metoclopramide, 10.2% in promethazine and 6.2% in placebo) Rate of N/V was not statistically significant between any of the groups. | Patients should receive antiemetic therapy only if experience N/V and not as a prophylactic agent with IV opioids. Patients that received (morphine + placebo) had less N/V compared to other treatment groups; however, NOT statistically significant. |
| Sussan et al. [9] Randomized, double- masked multicenter trial Performed in 9 countries | Investigated 2,574 patients that received IV opioids and randomized 520 patients that developed N/V associated with IV opioids. Group 1: placebo (n=94) Group 2: ondansetron 8 mg (n=214) Group 3: ondansetron 16 mg (n=211) | Resolution of N/V was statistically more significant (p < 0.001) when comparing ondansetron therapy with placebo. Group 1: 45.7% N/V resolved Group 2: 62.3% N/V resolved Group 3: 68.7% N/V resolved | The best practice seems to treat patients’ N/V after development in patients that receive IV opioids. Trial determined the prevalence of N/V is minimal and exposing patients to medication they do not need puts them at risk for additional adverse drug reactions. |
Each of the 3 trials concluded that there was no statistical significance in outcomes when adding prophylactic antiemetics with IV opioids. After these institutions analyzed their findings, the investigators at their respective institutions made it common practice for patients to only receive antiemetics AFTER a patient developed nausea or vomiting.
So why is ondansetron still commonly used to pre-treat patients that receive IV opioids in the ED?
The limited literature primarily focused on these anti-emetic agents: metoclopramide, promethazine, and ramosetron (5-HT3 antagonist). Literature related to specifically ondansetron is minimal.
Two randomized, placebo-controlled studies comparing ondansetron, metoclopramide, and saline in ED patients complaining of nausea showed no clinically important difference in the reduction of nausea between treatments and placebo [12, 13]. Yet in the ED, we still order ondansetron more than any other medication.
Some nerd (me!) put together a prospective multiple-site study (n=133) at 2 academic medical institutions where patients were administered IV opioids, with or without IV ondansetron [14]. Patients were observed for nausea and vomiting at baseline, 5 minutes, and 30 minutes after opioid administration, and then for a total of 2 hours. The results showed that 17.3% of patients developed nausea, with no significant difference in the rate of nausea, emesis, or the need for rescue antiemetics between the group receiving ondansetron and the group receiving opioids alone.
Of note, ondansetron is not FDA approved for the treatment or prophylaxis of acute nausea and/or vomiting (N/V) outside of chemotherapy, radiation, and postoperative use. It also, not surprisingly, has side effects!

What chemical substance is used to produce this smoke screen?
[Image from the National Museum of the U.S. Air Force, Wikimedia Commons]

What organism causes seabather’s eruption?
[Author’s own image]