|Year : 2021 | Volume
| Issue : 4 | Page : 217-220
A successful treatment with intravenous lipid emulsion therapy in a child with verapamil poisoning
, Tanıl Kendirli1
, Serhan Özcan1
, Melih Timuçin Doğan2
, Ahmet Onur Yiğit1
, Tayfun Uçar2 1 Department of Pediatric Intensive Care, School of Medicine, Ankara University, Ankara, Turkey
2 Department of Pediatric Cardiology, School of Medicine, Ankara University, Ankara, Turkey
|Date of Submission||23-Feb-2021|
|Date of Decision||06-Apr-2021|
|Date of Acceptance||17-May-2021|
|Date of Web Publication||29-Oct-2021|
Dr. Merve Havan
Division of Pediatric Critical Care Medicine, Ankara University Faculty of Medicine, Ankara
Source of Support: None, Conflict of Interest: None
In recent years, intravenous lipid emulsion therapy (ILE) was used for lipophilic drug intoxications, and successful results were obtained. In the literature, there is a small number of reported cases about verapamil intoxication and ILE therapy in the pediatric age group. We used ILE therapy in a 14-year-old girl with verapamil intoxication in the 2nd h of the pediatric intensive care unit stay, before using traditional treatments such as glucagon and hyperinsulinemic euglycemia. She had resistant bradycardia and hypotension which was unresponsive to inotropic agents and a successful result was obtained after using ILE treatment. We believe our report may contribute to the early use of ILE therapy for toxicity with calcium channel blockers such as verapamil in pediatric patients.
Keywords: Children, intoxication, lipid emulsion therapy, verapamil
|How to cite this article:|
Havan M, Kendirli T, Özcan S, Doğan MT, Yiğit AO, Uçar T. A successful treatment with intravenous lipid emulsion therapy in a child with verapamil poisoning. Turk J Emerg Med 2021;21:217-20
|How to cite this URL:|
Havan M, Kendirli T, Özcan S, Doğan MT, Yiğit AO, Uçar T. A successful treatment with intravenous lipid emulsion therapy in a child with verapamil poisoning. Turk J Emerg Med [serial online] 2021 [cited 2021 Nov 28];21:217-20. Available from: https://www.turkjemergmed.org/text.asp?2021/21/4/217/329626
| Introduction|| |
In recent years, intravenous lipid emulsion therapy (ILE) has been frequently used in the intoxications of anesthetic and lipophilic drugs after animal experiments. Initial studies were done in the late 1990s. ILE therapy began to be used for therapeutic purposes in the systemic toxicity of local anesthetic drugs in 2006, and then it was used for lipophilic drug toxicity, and successful results have been reported in intoxications with calcium channel blockers (CCBs), beta-blockers, neuroleptics, antidepressants, and anticonvulsants.
Hypotension and bradycardia are the most common symptoms in CCB intoxication. Metabolic acidosis and hyperglycemia are other common symptoms. In verapamil intoxication, there is no known antidote. Gastrointestinal decontamination is the first-line therapy. Intravenous calcium supplements, glucagon, hyperinsulinemic euglycemia (HIE) treatment, and in recent years, lipid emulsion therapy are recommended treatment methods in verapamil intoxication.
Here, we would like to report the early use of ILE therapy in verapamil intoxication in a 14-year-old girl who was followed with resistant hypotension and bradycardia in our pediatric intensive care unit (PICU).
| Case Report|| |
A 14-year-old girl was admitted to the pediatric emergency room with complaints of vomiting and dizziness. The patient stated that she had ingested 40 tablets verapamil (contains 120 mg verapamil hydrochloride in each tablet) 10 h before the emergency service admission. The patient underwent continuous cardiac monitoring. Her serial electrocardiography (ECGs) were obtained. On her physical examination, her body weight was 60 kg and her height was 157 cm. She was lethargic, her arterial blood pressure (BP), heart rate, respiration rate, and body temperature were measured as 57/32 mmHg, 50/min, 14/min, and 36.2°C, respectively. In the emergency department, gastric lavage and active charcoal treatment were not performed because she received the drug 10 h before the admission. 20 ml/kg 0.9% saline infusion has been given to the patient two times in the emergency department. The patient was taken to the PICU because her bradycardia and hypotension were resistant despite treatment. A central venous catheter was inserted quickly and 2500 ml/m2 hydration was started. In the laboratory analyses, complete blood count, renal function tests, serum electrolytes, and arterial blood gas analyses were taken, and all the results were within normal limits apart from elevated lactate levels (5.2 mml/L). Hyperglycemia was not found in the patient's blood glucose monitoring. In our follow-up, her general condition was poor and lethargic; bradycardia and ventricular extrasystoles were seen in the ECG [Figure 1]. She was in cardiogenic shock and dopamine infusion, at a rate of 10 mcg/kg/min was started, and calcium gluconate was given for CCB toxicity but her vital parameters did not change. Then, norepinephrine infusion therapy (0.1 mcg/kg/min) was started because she had peripheral vasodilatation symptoms and flushing. At the 2nd h of the patient's PICU hospitalization, we considered it appropriate to start ILE treatment, as the patient's hypotension and bradycardia continued, despite increased doses of inotropic drugs and calcium support. Intravenous lipid infusion (20% Intralipid) therapy was started at a rate of 1.5 ml/kg for 2 h. Half an hour after starting the ILE treatment, the patient's rhythm returned to the sinus rhythm, the ventricular extrasystoles disappeared on the patient's ECG and her arterial BP began to improve. The patient's BP was 79/52 mmHg when we started treatment. BPs were measured at 30 min, 1 h, and 2 h after the treatment had started, and the BPs were 84/56, 90/61, and 92/67 mmHg, respectively. Vital signs of the patient before and after ILE treatment are given in [Table 1]. After treatment, her inotropic drugs were gradually reduced within 8 h, and her consciousness began to recover very quickly. On the 2nd day of the intensive care stay, the patient was transferred to the cardiology service with complete neurological recovery and no organ failure. She was discharged from the hospital on the 4th day of admission. Detailed informed consent was obtained from the patient's parents in this case report.
|Table 1: The patient's vital signs before and after intravenous lipid emulsion therapy|
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|Figure 1: Sinus bradycardia and ventricular extrasystoles on electrocardiography of the patient before lipid emulsion therapy|
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| Discussion|| |
Verapamil is a nondhydropyridine CCB that is used in the treatment of arrhythmias, hypertension, and angina pectoris. Verapamil selectively blocks L-type calcium channels in the myocardium which are responsible for myocardial and vascular smooth muscle contractility. Verapamil toxicity causes peripheral vasodilation, hypotension, bradycardia, metabolic acidosis, hyperglycemia, congestive heart failure, pulmonary edema, and cardiac arrest. There is no specific antidote for verapamil overdose, and extracorporeal removal by hemodialysis is not effective. Orogastric lavage is useful if performed in the first 2 h after taking the drug, but vagal stimulation may exacerbate CCB-induced bradycardia and hypotension. We did not perform gastric lavage on our patient because she came to the emergency room 10 h after taking the drug, and we thought that orogastric lavage would not be beneficial and could worsen the patient's symptoms with vagal system activation.
Intravenous calcium supplements have been used for the treatment of cardiac side effects in verapamil toxicity. Glucagon has chronotropic and inotropic effects but is not effective in the recovery of bradycardia. HIE is a successful treatment for hypotension, hyperglycemia, and metabolic acidosis but has not been shown to have sufficient effect in the treatment of bradycardia, heart block, and intraventricular conduction delay. Our patient was in hypotensive shock, and she had refractory bradycardia. Despite intravenous saline bolus treatment, calcium gluconate, and high doses of inotropic agents, the patient's bradycardia and hypotension did not improve. Due to the absence of hyperglycemia during her admission and the fact that her main symptoms are secondary to cardiac pathology, we did not give HIE treatment as a priority.
In recent years, ILE therapy has been used in the emergency department for life-threatening drug intoxications. Although the effect of ILE therapy in the treatment of drug toxicity is still not fully known, two main mechanisms are emphasized in particular. First, the sweeping/portioning effect which is known as the lipid sink/shuttle phenomenon, and second, its direct cardiovascular effect since it acts on myocytes. In an in vitro study, traditional treatments such as calcium supplements, glucagon, and insulin used in verapamil toxicity were shown to not affect L-type calcium channels, but ILE therapy directly affects L-type calcium channels, restoring myocyte contractility. For this reason, we planned to give ILE treatment after calcium support and inotropic agents, as we thought we would see more benefits from ILE treatment than glucagon and HIE.
In the literature, there is no accurate information about when to start ILE treatment for lipophilic drug toxicity, what dose to apply, and whether bolus treatment or continuous infusion is more useful. Previous publications on the use of ILE therapy in patients with verapamil poisoning are presented in detail in [Table 2].There are only a few cases related to the use of ILE therapy in verapamil poisoning, and when these cases are examined, it has been reported that ILE therapy benefits some and does not provide the expected benefit in others [Table 2]. Furthermore, there are not enough publications on the use of ILE therapy in verapamil poisoning in pediatric patients. In a study that identified 14 cases, all patients were given different doses of bolus and/or continuous ILE therapy, and treatment doses were reported to vary according to the experience of clinicians. In another study, blood verapamil levels were measured after poisoning, and the measured level was reported to be decreased after ILE treatment. In our study, we were unable to measure blood verapamil levels. In the literature, there is no definitive data on the administration dose of ILE therapy in the pediatric age group. We administered 1.5 g/kg 20% lipid solution as an intravenous infusion for 2 h, avoiding giving a bolus dose, because our patient was a child, and we thought that lipid treatment at a bolus dose might have side effects.
|Table 2: Recent publications reporting the use of intravenous lipid emulsion therapy in verapamil poisoning|
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ILE treatment also can have serious side and adverse effects. In adults, hyperlipidemia, increased bleeding tendency, hypokalemia, hypophosphatemia, local thrombophlebitis, acute lung damage, hemolysis, and acute pancreatitis have been reported. In our case, we did not see any complication about medication.
ILE treatment was stated to be beneficial in lipophilic drug poisoning. In the literature, it is recommended to use ILE therapy after standard treatment protocols (calcium support, glucagon, and HIE) for verapamil poisoning and to use extracorporeal treatment methods if the benefit is still not achieved. We applied ILE therapy to our case before applying much more invasive extracorporeal treatment methods such as hemoperfusion and extracorporeal membrane oxygenation. After starting ILE treatment, the patient's clinical manifestations quickly improved, and we began to reduce the infusion doses of inotropic agents, and the patient's consciousness quickly improved.
| Conclusion|| |
This case report may be useful to show that good results can be achieved using early-stage ILE therapy in pediatric patients with verapamil poisoning. As the number of studies on ILE use in children increases, this method of treatment will be used more often in lipophilic drug poisoning.
In this case report everyone who contributed to this manuscript is listed as an author.
Author contributions statement
Merve Havan: Conceptualization (lead); writing – original draft (lead); Methodology (lead). Tanıl Kendirli: Supervision (lead); Visualization (lead). Serhan Özcan: Methodology (lead); Resources; Writing – original draft (supporting). Melih T. Doğan: Resources (supporting). Onur Yiğit: Resources Writing – original draft (supporting). Tayfun Uçar: Writing – review and editing (equal).
Conflicts of interest
Consent to participate
The authors certify that they have obtained all appropriate patient consent forms. In the form, the parents have given their consent for images and other clinical information to be reported in the journal. The parents understand that names and initials will not be published, and due efforts will be made to conceal identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
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[Table 1], [Table 2]