Case Reports

CASE REPORT – Monitored anesthesia care with dexmedetomidine and remifentanil during cardiac catheterization in a patient with Duchenne muscular dystrophy and malignant hyperthermia susceptibility

Alok Moharir, MD, Joseph D. Tobias, MD

Departments of Anesthesiology & Pain Medicine, Nationwide Children’s Hospital and the Ohio State University, Columbus, Ohio (USA)

Correspondence: Joseph D. Tobias, MD, Chairman, Department of Anesthesiology & Pain Medicine, Nationwide Children’s Hospital, 700 Children’s Drive, Columbus, Ohio 43205 (USA); Phone: (614) 722-4200; Fax: (614) 722-4203; E-mail: Joseph.Tobias@Nationwidechildrens.org

ABSTRACT

Sedation during invasive procedures is frequently required not only to provide appropriate humanitarian care, but also to facilitate the completion of invasive procedures. Although the current sedative agents are generally safe and effective, adverse effects may occur especially in patients with co-morbid diseases. We present the successful use of a combination of dexmedetomidine and remifentanil to provide sedation (monitored anesthesia care) during cardiac catheterization and coronary angiography in an 11 years old patient with Duchenne muscular dystrophy. Co-morbid conditions included depressed myocardial function, a recent concern of coronary artery insufficiency, a family history of malignant hyperthermia, and impaired respiratory function. Dexmedetomidine was administered as an infusion starting at 0.7 μg/kg/hour without a loading dose, while remifentanil was administered as an infusion of 0.1 µg/kg/min. There was no patient response to local infiltration of the groin or placement of the arterial catheter for coronary angiography. The patient tolerated the procedure well without adverse effects. The combination of dexmedetomidine and remifentanil for monitored anesthesia care in the pediatric patient is discussed and the potential efficacy of this combination for procedural sedation is reviewed.

Key words: Dexmedetomidine; Remifentanil; Sedation; Monitored anesthesia care; Duchenne muscular dystrophy; Malignant hyperthermia; Co-morbid diseases

Citation: Moharir A, Tobias JD. Monitored anesthesia care with dexmedetomidine and remifentanil during cardiac catheterization in a patient with Duchenne muscular dystrophy and malignant hyperthermia susceptibility. Anaesth Pain & Intensive Care 2013;17(3):__

INTRODUCTION

General anesthesia is generally required for cardiac catheterization in the pediatric population although sedation or monitored anesthesia care (MAC) may also be used.1,2 The use of effective sedation or general anesthesia not only allows the control of hemodynamic parameters, but also ensures a motionless patient thereby facilitating the timely completion of the procedure. During procedural sedation, the incidence of adverse effects has been reported to be higher in patients with underlying co-morbid conditions especially those involving the cardiac or respiratory system.3

Duchenne muscular dystrophy (DMD), an x-linked disorder with an incidence of 1 in 3,300 male births, generally presents as weakness between 4 and 8 years of age. This genetic defect results in a deficiency of the dystrophin protein in skeletal, cardiac, and smooth muscle. Skeletal muscle involvement predominates as the major clinical feature of this disorder during the first decade of life. However, as these patients enter the 2nd and the 3rd decade of life, progressive myocardial involvement leads to impaired myocardial contractility, conduction disturbances, and arrhythmias. Given the involvement of both cardiac and respiratory function, there is a significantly increased risk during anesthetic care of these patients.4,5  When endotracheal intubation is necessary for anesthetic care, postoperative mechanical ventilation may be required.6,7

Although general anesthesia may be required for specific surgical procedures, sedation or MAC with the maintenance of spontaneous ventilation may be chosen for even moderately painful procedures such as cardiac catheterization. In such cases, there are many options although frequently used agents such as propofol may result in respiratory depression.8-10 We report our novel experience with a combination of dexmedetomidine and remifentanil for sedation during cardiac catheterization and coronary angiography in an 11-year-old patient with Duchenne muscular dystrophy, co-morbid respiratory and cardiac involvement, a family history of malignant hyperthermia (MH), and suspected coronary artery ischemia. The potential applications of this combination in procedural sedation are discussed and previous reports from the literature reviewed.

CASE REPORT

Institutional Review Board approval is not required at Nationwide Children’s Hospital (Columbus, Ohio) for the presentation of single patient case reports.  The patient was an 11-year-old, 31 kilogram boy who presented to the cardiac catheterization laboratory for a diagnostic coronary angiography. He had a history of Duchenne muscular dystrophy and dilated cardiomyopathy. There was also a strong family history of MH in first degree relatives. He had presented to the hospital with a one day history of substernal chest pain radiating down his left arm. Further workup revealed an elevated serum troponin level and an electrocardiogram with ST segment elevation in the inferior leads. An echocardiogram performed that day showed worsening left ventricular function with an ejection fraction of 42% and new areas of dyskinesis of the basilar and inferior wall. Therapy included a dose of acetylsalicylic acid, supplemental oxygen via nasal cannula, a heparin infusion at 12 units/kg/hr, and a nitroglycerin infusion at 1 μg/kg/min. The anesthesia machine was flushed with high flow oxygen, the soda lime canister was replaced, and the anesthesia vaporizers were removed per the departmental MH protocol. The patient was held nil per os for 6 hours and transported to the cardiac catheterization suite. Premedication included 2 mg of intravenous midazolam. Standard American Society of Anesthesiologists’ monitors were placed including a nasal cannula with end tidal carbon dioxide (EtCO2) monitoring capability. A second peripheral intravenous cannula was inserted. Dexmedetomidine and remifentanil were started at 0.7 μg/kg/hr and 0.1 μg/kg/min, respectively. After ensuring an adequate depth of sedation, the groin was infiltrated with 1% lidocaine. There was no patient response to the injection of the local anesthetic agent. The right femoral artery was also cannulated without response. The patient’s heart rate and respiratory rate remained within 20% of baseline. His pulse oximetry reading remained above 96% on 3 lit/min of oxygen with an EtCO2 of 36-44 mmHg. There was an initial drop in systolic blood pressure of 20% when the infusions were started. After discussion with the cardiologist, it was determined that the nitroglycerin could be discontinued as his chest pain had resolved. With the discontinuation of the nitroglycerin infusion and a 10 ml/kg bolus of lactated ringer’s solution, his systolic blood pressure promptly returned to baseline. An arterial blood gas obtained during the procedure revealed: pH 7.33, CO2 47.9 mmHg, PaO2 218 mmHg, HCO3 25.4 mEq/lit with an SpO2 of 100% on 3 lit/min of oxygen. During the procedure, it was necessary to upsize the femoral artery catheter. Prior to this, the remifentanil infusion was increased to 0.15 μg/kg/min. There was no patient response to the catheter change. Coronary angiography did not reveal any occlusive disease of the coronary arteries and the procedure was completed in 45 minutes. The femoral artery catheter was removed and adequate hemostasis was achieved. The dexmedetomidine and remifentanil infusions were discontinued. The patient was awake and conversing within 5 minutes. He was transported to the Cardiothoracic Intensive Care Unit with standard monitors and supplemental oxygen at 3 liters/minute via nasal cannula. The ST elevation which had occurred prior to the procedure resolved during the case. In the immediate post-procedure period, the patient complained of pain in the right groin which was treated with hydromorphone 10 μg/kg. There were no other complications during the hospital stay. The patient was discharged home on postoperative day 2 with planned follow-up with his cardiologist in the outpatient setting.

DISCUSSION

Our patient presented with multiple co-morbidities which might be expected to increase the risk for adverse events. Significant co-morbid conditions included cardiac and respiratory involvement related to DMD, a family history of MH, which excluded the use of volatile anesthetic agents for general anesthesia, and clinical evidence suggestive of coronary artery ischemia. In patients with MH, a total intravenous anesthetic technique using propofol is most commonly chosen for sedation or general anesthesia. Numerous studies have reported the efficacy of propofol for monitored anesthesia care for pediatric patients undergoing invasive and non-invasive procedures.8-10 However, propofol can cause a significant decrease in cardiac contractility, mean arterial pressure, and systemic vascular resistance. Additional cardiovascular effects may be caused by augmentation of central vagal tone leading to bradycardia, conduction disturbances and asystole.11,12 Given our patient’s limited cardiovascular reserve and the potential coronary artery ischemia, there was the concern that propofol may decrease diastolic blood pressure and thereby impact myocardial oxygen supply and coronary perfusion pressure. An additional concern was the potential for respiratory depression related to a direct inhibition of upper airway muscle activity and a centrally mediated inhibition of airway reflexes.

Dexmedetomidine is an α2-adrenergic agonist which initially received FDA approval in the United States in 1999 for the sedation of adults during mechanical ventilation and subsequently in 2009 for monitored anesthesia care (MAC) of adults. While FDA approved it only for use in adults, dexmedetomidine has been used safely and successfully in several different clinical scenarios in infants and children including sedation during mechanical ventilation, procedural sedation, supplementation of postoperative analgesia, prevention of emergence delirium, control of post-anesthesia shivering, and the treatment of withdrawal.13 Dexmedetomidine has also been used as a primary anesthetic agent in patients undergoing surgery who are susceptible to malignant hyperthermia.14-16 Through its agonistic effects at central α2-adrenergic receptors, dexmedetomidine exerts a negative chronotropic effect resulting in a decrease in heart rate and a reduction in central sympathetic outflow, both of which are ideal in patients at risk for coronary artery ischemia. When compared with propofol, the respiratory depressant effects of dexmedetomidine are limited.10 Although generally effective for sedation during non-invasive procedures, its use as a sole agent has not been uniformly successful for invasive procedures.17-19

One potential option is to supplement sedation with ketamine. Ketamine has both analgesic and sympathomimetic properties, making it an ideal complement to dexmedetomidine.20 This combination has been used successfully for MAC in pediatric patients undergoing cardiac catheterization.21 Although dexmedetomidine has been shown to blunt the sympathetic response to ketamine, given our patient’s clinical suspicion of coronary ischemia, we chose not to use ketamine given the potential for tachycardia and hypertension.

Analgesia is a key component of procedural sedation especially in patients with ischemia to prevent an increase in myocardial oxygen demand related to hypertension or tachycardia. We chose remifentanil for its intense analgesia, rapid onset, quick metabolism, and easy titration by continuous infusion. The latter may be particular relevant during cardiac catheterization when intense analgesia is required for brief periods such as during cannulae placement. Analgesia was further supplemented by the liberal use of local anesthetic infiltration at the insertion site. Additionally, remifentanil has limited direct myocardial depressant effects. One concern regarding remifentanil relates to its respiratory depressant effects which may be particularly problematic when the maintenance of spontaneous ventilation is desired.22 However, given its rapid metabolism, its respiratory depressant effects would be readily reversible with discontinuation of the infusion. Additionally, albeit rare, a unique adverse effect noted with the synthetic opioids is chest wall rigidity.23 This has been most commonly reported with bolus dosing, but may occur with infusions. To date, there are limited reports regarding the combination of dexmedetomidine and remifentanil for procedural sedation or general anesthesia. Burnett et al reported the use of these agents as the primary components of a general anesthesia in a patient with a mitochondrial myopathy.24 Arpaci and Bozkirh described the successful use of a remifentanil-dexmedetomidine combination for sedation in adults undergoing cystoscopy.25 However, to date there are no reports regarding this combination for monitored MAC or procedural sedation in pediatric patients.

In summary, our anecdotal experience highlights the effective use of a combination of dexmedetomidine and remifentanil for sedation in a pediatric patient with multiple co-morbid conditions including DMD, MH history, and clinical concerns of coronary ischemia. Effective sedation was provided by continuous infusions of both agents starting at 0.1 µg/kg/min for remifentanil and 0.7 µg/kg/hour for dexmedetomidine. We chose not to use a bolus infusion given the potential for adverse hemodynamic and respiratory effects in a patient with co-morbid conditions. Using this combination supplemented with local anesthetic infiltration, we noted minimal changes in hemodynamic parameters, oxygenation saturation, and ventilation. Emergence from sedation was rapid. Given the potential for adverse effects on hemodynamic and respiratory function with any sedation regimen, we would recommend adherence to the guidelines from the American Academy of Pediatrics for monitoring and care of the pediatric patient during procedural sedation.26

REFERENCES

  1. Abbas SM, Rashid A, Latif H. Sedation for children undergoing cardiac catheterization: a review of literature. J Pak Med Assoc 2012;62:159-63. [PubMed]
  2. Javorski JJ, Hansen DD, Laussen PC, Fox ML, Lavoie J, Burrows FA. Paediatric cardiac catheterization: innovations. Can J Anaesth 1995;42:310-29. [PubMed]
  3. Malviya S, Voepel-Lewis T, Eldevik OP, Rockwell DT, Wong JH, Tait AR. Sedation and general anaesthesia in children undergoing MRI and CT: adverse events and outcomes. Br J Anaesth 2000;84:743-8. [PubMed] [Free full text]
  4. Sethna NF, Rockoff MA, Worthen HM, Rosnow JM (1988). Anesthesia-related complications in children with Duchenne muscular dystrophy. Anesthesiology 1988;68:462-5. [PubMed] [Free full text]
  5. Cripe LH, Tobias JD. Cardiac considerations in the operative management of the patient with Duchenne or Becker muscular dystrophy. Paediatr Anaesth. 2013 Sep;23(9):777-84. doi: 10.1111/pan.12229. Epub 2013 Jul 19. [PubMed]
  6. Harper CM, Ambler G, Edge G. The prognostic value of preoperative predicted forced vital capacity in corrective spinal surgery for Duchenne’s muscular dystrophy. Anaesthesia 2004;59:1160-2. [PubMed]
  7. 7.     Almenrader N, Patel D. Spinal fusion surgery in children with non-idiopathic scoliosis: is there a need for routine postoperative mechanical ventilation? Br J Anaesth 2006;97:851-7. [PubMed] Epub 2006 Oct 11. [Free full text]
  8. Cravero JP, Beach ML, Blike GT, Gallagher SM, Hertzog JH; Pediatric Sedation Research Consortium. The incidence and nature of adverse events during pediatric sedation/anesthesia with propofol for procedures outside the operating room: a report from the Pediatric Sedation Research Consortium. Anesth Analg 2009;108:795-804. [PubMed] doi: 10.1213/ane.0b013e31818fc334.
  9. Hertzog JH, Dalton HJ, Anderson BD, Shad AT, Gootenberg JE, Hauser GJ. Prospective evaluation of propofol anesthesia in the pediatric intensive care unit for elective oncology procedures in ambulatory and hospitalized children. Pediatrics 2000;106:742-7. [PubMed]
  10. Koroglu A, Demirbilek S, Teksan H, Sagir O, But AK, Ersoy MO. Sedative, hemodynamic and respiratory effects of dexmedetomidine in children undergoing magnetic resonance imaging examination: preliminary results. Br J Anaesth 2005;94:821-4. [PubMed] Epub 2005 Mar 11.
  11. Sochala C, Van Deenen D, De Ville A, Govaerts MJM. Heart block following propofol in a child. Paediatr Anaesth.1999;9:349-51. [PubMed]
  12. Egan TD, Brock-Utne JG. Asystole and anesthesia induction with a fentanyl, propofol, and succinylcholine sequence. Anesth Analg 1991;73:818-20. [PubMed]
  13. Tobias JD. Dexmedetomidine: Applications in pediatric critical care and pediatric anesthesiology. Pediatr Crit Care Med 2007;8:115-31.  [PubMed]
  14. Dewhirst E, Naguib A, Tobias JD. Dexmedetomidine as part of balanced anesthesia care in children with malignant hyperthermia risk and egg allergy. J Pediatr Pharmacol Ther 2011;16:113-7. [PubMed] doi: 10.5863/1551-6776-16.2.113.
  15. Naguib A, McKee C, Phillips A, Tobias JD. Dexmedetomidine as the primary anesthetic agent during cardiac surgery in an infant with a family history of malignant hyperthermia. Saudi J Anaesth 2011;5:426-9. [PubMed] [Free full text]doi: 10.4103/1658-354X.87276.
  16. Unger RJ. General anesthesia with dexmedetomidine in a malignant hyperthermia-susceptible woman. Acta Anaesthesiol Scand 2006;50:1312-3. [PubMed]
  17. Munro HM, Tirotta CF, Felix DE, Lagueruela RG, Madril DR, Zahn EM, et al. Initial experience with dexmedetomidine for diagnostic and interventional cardiac catheterization in children. Paediatr Anaesth 2007;17:109-12. [PubMed]
  18. Jalowiecki P, Rudner R, Gonciarz M, Kawecki P, Petelenz M, Dziurdzik P. Sole use of dexmedetomidine has limited utility for conscious sedation during outpatient colonoscopy. Anesthesiology 2005;103:269-73. [PubMed] [Free full text]
  19. Alhashemi JA. Dexmedetomidine vs. midazolam for monitored anaesthesia care during cataract surgery. Br J Anaesth 2006;96:722-6. [PubMed] [Free full text]
  20. Tobias JD. Dexmedetomidine and ketamine: An effective alternative for procedural sedation? Pediatr Crit Care Med 2012;13:423-7. [PubMed] doi: 10.1097/PCC.0b013e318238b81c.
  21. Mester R, Easley RB, Brady KM, Chilson K, Tobias JD. Monitored anesthesia care with a combination of ketamine and dexmedetomidine during cardiac catheterization. Am J Ther 2008;15:24-30. [PubMed] doi: 10.1097/MJT.0b013e3180a72255.
  22. Litman RS. Conscious sedation with remifentanil during painful medical procedures. J Pain Symptom Manage. 2000;19:468-71. [PubMed]
  23. Dewhirst E, Naguib A, Tobias JD. Chest wall rigidity in two infants after low-dose fentanyl administration. Pediatr Emerg Care 2012;28:465-8. [PubMed] doi: 10.1097/PEC.0b013e3182535a2a.
  24. Burnett T, Schwartz L, Tobias J. Anaesthesia with dexmedetomidine and remifentanil in a child with mitochondrial myopathy. South Afr J Anaesth Analg 2011;17:262-4.
  25. Arpaci AH, Bozkırh F. Comparison of sedation effectiveness of remifentanil-dexmedetomidine and remifentanil-midazolam combinations and their effects on postoperative cognitive function in cystoscopies: A randomized clinical trial. J Res Med Sci 2013;18:107-14. [PubMed] [Free full text]
  26. American Academy of PediatricsAmerican Academy of Pediatric Dentistry, Coté CJ, Wilson S; WorkGroup on Sedation. Guidelines for monitoring and management of pediatric patients during and after sedation for diagnostic and therapeutic procedures. Pediatrics 2006;118:2587-602. [PubMed] [Free full text]