Create Account




Forget Password

Authors

Hatice Akpınar
SDÜ Diş hekimliği Fakültesi

Who liked this


No one liked this yet.

Followers


General anaesthesia in a patient with Edwards Syndrome: A Case Report

Submitted : 12.09.2018
Accepted : 16.10.2018
Published : 03.12.2018

Abstract

Edwards syndrome (ES) is a syndrome with severe fatal anomalies resulting from malformations of the 18th chromosome seen in 8000 live births. The male / female ratio is 1/4. Ninety percent of newborn babies die in the first twelve months. Patients have moderate mental retardation, muscle hypotonia and extremity anomalies, microcephaly, facial anomalies, developmental disorders, scoliosis, epilepsy, severe cardiac and urogenital anomalies. In a limited number of literature on ES, all cases were anesthetized to exclude lethal causes and emergencies. Our aim in presenting this case is to discuss the experience of anesthetic management of a 13-year- old patient with ES. He has undergone an elective and trouble-free operation and his dental treatments were successfully completed.

Introduction

Edwards syndrome (ES) is a syndrome associated with severe fatal anomalies resulting from malformations in the 18th chromosome, seen in 1/ 8000 live births. The ratio of male to female is 1/4. Ninety percent of the babies born are lost in the first twelve months 1. Patients have moderate mental retardation, muscular hypotonia, extremity anomalies, microcephaly, facial anomalies, developmental failures, scoliosis, epilepsy,  serious cardiac anomalies and urogenital anomalies 2. In a limited number of literature on ES, all cases were anesthetized in urgent conditions,  in order to rule out the fatal causes. Our goal in presenting this case is to share with you the experience of anesthetic management of a 13-year-old patient with ES.  patientwhich is passed through the elective operation in advanced age and the problem of the anesthesia which is due to the drugs and the conditions used in the literature.

Case Report

A 13-year-old-boy weighing 73 kg  was admitted to the polyclinic because of his toothache. At 2 years old, he was diagnosed with ES. 18th chromosome as short-choked microbes was  confirmed genetically.  Serious laryngospasm developing against radiopaque material given when brain MRI is withdrawn at 2.5 years, In the examination of the patient, he had dysmorphic facial appearance, and  jaw and tooth structure was anatomically different. There were  speech disturbance at advanced level and moderate mental retardation. There was a murmur in the mitral focus. He had Hb: 11 mg dl-1. On  echocardiogram,  patent foramen ovale, pulmonary stenosis, grade I mitral insufficiency, right renal atrophy with frequent infection due to athrophic kidney were detected. He was evaluated as  ASA III and mallampati 2. On the operation day, the patient was premedicated with oral midazolam 5 mg. Standard monitorization was performed. The pulse was recorded as 90 beats/min, TA 100/70 mmHg, SPO2 99% and the measurement continued at 5 minute intervals. The patient without vascular access was given induction of inhalation with 8% sevoflurane + 100% O2. 22 G  intravenous cannula was   inserted, and 2 mg kg-1 propofol and 0.5 mg kg-1 rocuronium bromide were given.  When respiratory depression was present, the mask was ventilated for 3 minutes with 6 lt min-1 O2 via balloon. After satisfactory muscle relaxation was achieved, portex 7 cuffed endotracheal tube intubation was performed ( Figure 1).

Figure 1
Shows the patient with Edwards syndrome under general anesthesia

 

After intubation, laryngospasm developed and the patient was treated with prednisolone 1mg kg-1. %40 O2-%60 N2O- 2%  anesthesia was maintained with sevoflurane. Following local infiltration anesthesia, the patient's teeth numbered 12, 16, 24, 26, 46 were filled. The patient received prophylaxis of 2gr  penciline+sulbactam.  Thirty  minutes after this procedure,  tooth 25  was extracted (Figure2-3).

 

Figure 2
The patients panoramic x-ray
Figure 3
Intraoral image after the dental treatment

 

The process took a total of 75 minutes. Decurarization was performed  via 2 mg kg-1 sugammadex administration at the end of the operation. For postoperative pain treatment, 10 mg kg-1 paracatemol was infused for 30 minutes. Mr. ABU provided  informed consent for publication of his case.

Discussion

Although ES is a rare syndrome, it is the second most common chromosomal disorder accompanied by many anomalies. The rate of cardiac anomalies is 95% and it is the main responsibility of bad prognosis 1-3.  Our patient was being followed-up  for pulmonary stenosis  by cardiologists. İnfectious endocarditis prophylaxis is recommended in these patients before teeth extraction 4.  Dental treatments are performed under sedation or general anesthesia since mental retardation patients cannot cooperate.  We preferred general anesthesia for our patient because the duration of the procedure was long. Patients  usually  require  premedication before surgery 1.

Because the vein access at the beginning  was not achieved after oral premedication we were induction with inhalation in the surgery  room. For the cases where fatal anomalies are common in the literature, we recommend the  shortest possible anesthesia and the least invasive procedure, so we preferred sevoflurane and propofol for our short duration of action.

We could not achieve  vein access at the beginning,   but  after oral premedication, an IV line was  secured and  anesthesia was indused by  inhalation in the surgery room.  In the literature, the shortest possible anesthesia and the least invasive procedures are recommeded for  patients with fatal anomalies so we preferred sevoflurane and propofol for our patient 1,5. The article published by Sato et al., also mentioned a case of serious airway problem treated with sevoflurane 3,5. Depolarising agents for muscle relaxant use are not recommended because of the risk of malignant hyperthermia, but short-acting nondepolarizans can be used 1,2. The reason we prefer  rocuronium bromide (Myocron, vem ilaç sanayi) as a muscle relaxant is that it has a specific antidote which is sugamadex(Bridion MSD ilaç). This drug can convert the rocuronium bromide connected block to any level.

We did not use atropine-neostigmine because of cardiac side effects. Alternative airway devices, such as laryngeal mask airway (LMA), must be available for the difficult anatomy of  patients, especially for patients with facial and oral teeth anomalies 1. In our patient, all necessary equipment and LMA for intubation were available and the intubation was successfully performed with videolaringoscopy. Assessing pain in these patients is difficult because of communication problems. We did not need any long lasting narcotic analgesics  during the procedure. 

We provided pain control with infiltration anesthesia. There are publications suggesting sublimation of narcotic analgesics 2,3, but we preferred  remifentanil as a short-acting narcotics and as soon as possible effective narcotics.

 After a while,  our patient became agitated. We used paracatemol in the treatment of pain control  and the patient calmed down.  Different genetic variations related to the chromosome 18  have been mentioned in the literatüre 6,7.  In our case, multiduplication was detected in the short arm of the 18th chromosome. Genetic variations can affect the life span of the patient. Major cardiac anomalies may cause saturation level increase during positive pressure ventilation due to right-sided bag during general anesthesia. There are publications suggesting norepinephrine or dopamine for the treatment 8. We have tried to protect the spontaneous breathing of the patient as much as possible and have kept the positive pressure ventilation short .

ES may be missed in many cases due to major cardiac anomalies at an early age. New treatment techniques developed  every day, use of new drugs and increase in prenatal diagnosis by the use of  genetic tests  prolonged  life expectancy in these patients. There are few reports in the literature  that fully explain  anesthesia management in these patients. Keeping the procedure as short as possible and avoiding any invasive procedures and complications, protect  the patient from arrhythmia  and cardiac and pulmonary hemostasis and provide hemodynamic stability and  a smooth anesthetic process .   By maintaining a strict adherence to the above procedures, patients with ES can be discharged in a healthy manner with rapid recovery at the end of  a  procedure.

References

  1. Courre`P, Nıeuvıarts R, Lecoutre D. Anaesthetic management for Edward’s syndrome. Paediatr Anaesth.  2003; 13: 267-9.
  2. Schwemmle C, et al. Tetrasomie 18p und Innenohrschwerhörigkeit. HNO 2012; 60: 901-5.
  3. Arun O, et al. Anesthetic management of a newborn with trisomy 18 undergoing closure of patent ductus arteriosus and pulmonary artery banding. Cardiovasc J Afr.   2014; 25(4): 10-12.
  4. Plicht B, Lind A, Erbel R. Infective endocarditis : New ESC guidelines 2015. İnternist.  (Berl)  2016 ;57(7): 675-90.
  5. Sato Y, et al. Severe airway obstruction relieved by sedation using sevoflurane in a pediatric patient with tracheobronchomalacia.  MASUI The Japanese Journal of Anesthesiology. 2005; 54(2): 166-8.
  6. Plaiasu  V, et al. A rare chromosomal disorder–isochromosome 18p syndrome. Maedica. 2011; 6(2): 132-6.
  7. Dundar  M, et al. A case with a rare chromosomal abnormality: isochromosome 18p. Genet Couns.   2010; 21(1): 69-74.
  8. Hoon SK,et al.  Hypoxia due to positive pressure ventilation in Edwards’ syndrome: A case report.  J  Int  Med  Res. 2018; 46(2): 895-900.
Keywords : Edwards Sendromu , Genel Anestezi , Dental Tedavi

Comments

Login for send comment.