anesthesia for rare co-existing diseases alexandru apostol, m.d
TRANSCRIPT
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Anesthesia for Rare Co-existing Diseases
Alexandru Apostol, M.D.
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The most common cause of Dwarfism Autosomal dominant Mutations of FGFR3 receptor Large head, facial hypoplasia, spine
deformation, trident hand
Achondroplasia
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Difficult IV, mask ventilation, intubation Risk for Cervical cord ischemia OSA, CSA, PHTN Restrictive lung disease GERD Difficult RA
Achondroplasia & Anesthesia
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Mutation of UB3A gene, abnormal GABAR Developmental delay Movement dysfunction Minimal speech, nonverbal communication Microcephaly, seizures Prognathia
Angelman SyndromeHappy Poppet Syndrome
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Dysregulation of GABA, NMDA, AMPA Difficult RA Bradycardia Syncope Seizure disorder
Angelman & Anesthesia
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Malformation of the skull, hands, feet and face Mutation of fibroblast growth factor receptor 2
gene Craniosynostosis, Brachycephaly, mid -face
hypoplasia, Hypertelorism, increased ICP,syndactyly
Cardiac defects, polycystic kidney, pyloric stenosis
OSA, CSA
Apert SyndromeAcrocephalosyndactyly
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Difficult IV Difficult mask ventilation High incidence of Bronchospasm No reported difficult intubations Might need CPAP post op Avoid sedatives and Opiods
Apert Syndrome & Anesthesia
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Intrauterine fetus joint contractures, 3 degrees of severity
Type 1 affects extremities Type 2 affects extremities + scoliosis+ CDH Type 3 affects CNS
Arthrogryposis Multiplex Congenita
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Difficult IV Spinal and caudal might be difficult Possible cervical spine instability 25% difficult intubation Difficult positioning for surgery Risk of bleeding if on Valproic acid
Arthrogryposis Multiplex Congenita & anesthesia
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Inherited dominant neuromuscular disorder= congenital myopathy
25% association with MH Hypotonia, motor developmental delay, with
predominantly proximal weakness Cardiomyopathy rare When associated with scoliosis echo and
PFTs are needed
Central core diseaseShy-McGee Syndrome
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MH avoidance technique (no Succinylcholine no volatile anesthetics)
TIVA and RA are safe Neurological consult before RA for Juridical
reasons Pre-op CK level may be helpful Higher intr-aop blood loss during scoliosis
surgery
Central core disease & Anesthesia
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Coloboma Heart defect Atresia Choanae Retarded Growth and Development Genital Hypoplasia Ear Anomalies/Deafness Cleft lip and palate TEF
CHARGE SyndromeHall – Hittner Syndrome
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Inhalation induction may be difficult RSI preferred Difficult intubation Risk of aspiration Risk of arrhythmias Prolonged post-op mechanical ventilation
CHARGE Syndrome & Anesthesia
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Most common & severe muscular dystrophy Mutation in dystrophin gene on Chromosome
Xp21 Progressive skeletal muscle weakness Fatty and fibrous infiltration of muscles Age of diagnosis 3-5 years Risk of aspitation Cardiomyopathy (TEE)
Duchenne muscular dystrophyDystrophinopathy
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GA with TIVA Prolonged muscle relaxant effects Avoid Succinylcholine and VA Risk of hyperkalemic cardiac arrest or sever
rhabdomyolysis No risk of MH short use of VA is possible Avoid NO2 in case of cardiac involvement RA can be done
Duchenne muscular dystrophy & Anesthesia
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Group of inherited diseases with trauma induced blister formation of skin and mucosa
Deficiency of structural proteins of the dermo -epidermal junction
Microstomia, ankyloglosson and dental decay Cardiomyopathy GERD Anemia
Epidermolysis bullosa
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Difficult airway Prevent friction and trauma, lubrication of FM,
LMA, ETT, secure ETT with non adhesive LMA, ETT one seize smaller Extensive padding Infection prophylaxis Good pre-op sedation, RSI RA is OK but less skin infiltration with LA Patting the skin for disinfection
Epidermolysis bullosa & Anesthesia
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Vascular lesion with consumptive coagulopathy and throbocytopenia
Vascular tumor with irregular nodules Pt on Steroids, Vincrstine, Interferon,
Ticlopidine and or Aspirin Avoid Platelet transfusion due to trapping in
the tumor Heart failure secondary to massive AV shunts
Kasabach-Merritt SyndromeHemangioma-Thrombopenia
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Difficult airway No nasal intubation Avoid platelet transfusion Correct coagulopathy ( fibrinogen,
tranexamic acid) Side effects from Chemotherapy RA (aware of thrombocytopenia)
Kasabach-Merritt & Anesthesia
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Lysosomal storage disease Defective N –acetylglucosamine 1-phosphotransferase Accumulation of carbohydrate, lipids in various tissues
and organs The phenotype resemble Hurler Syndrome Jaw and neck may be stiff Short neck Thickened epiglottis, enlarged adenoids Cardiomyopathy, PHTN
Mucolipidosis II and III
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Difficult airway , FOI Difficult LMA ETT smaller than predicted Difficult IV OSA
Mucolipidosis II and III & Anesthesia
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Genetic disorder of chromosome 15 Hypothalamic-Pituitary abnormality Hypotonia in infancy, hyperphagia, morbid
obesity Behavioral problems OSA Cardiomyopathy Seizure disorder
Prader-Willi SyndromePrader-Labhardt-Willi
Syndrome
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Difficult airway management Difficult landmarks for RA Difficult IV High risk for bronchospasm High risk for aspirtation Potential for prolonged effects of NMB Safe to use succinylcholine Ketamine can be use with caution
Prader-Willi Syndrome & Anesthesia
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Genetic etiology of chromosome 7 and 11p15
Growth retardation Face and limb asymmetry Relative macrocephaly prominent for-head Hypospadias Anterior and small larynx Subglottic stenosis Retrognathia and hypognathia Risk of hypoglycemia
Russel - Silver SyndromeRussel - Silver Dwarfism
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Difficult airway due to facial dysmorphysm, retrognathia, hypognathia, small mouth opening,
Difficult mask ventilation RA can be used Ambulatory surgery is not recommended
Russel - Silver Syndrome & Anesthesia
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Autosomal dominant Almost exclusively found in Sweden and
Finland Late adult onset Weakness and atrophy of distal muscles Inability to extend the fingers Decreased DTR No cardiac involvement
Welander Distal Myopathydistal myopathy Swedish type
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GA and RA not contraindicated PT with RLS no Etomidate or Propofol Careful use of NMB
Welander Distal Myopathy & Anesthesia
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It can be congenital or acquired Causes of acquired are :Quinidine, Disopyramide,
TCA, SAH, hypokalemia, hypomagnesaemia, right neck dissection
The pathognomonic feature is prolonged Q-T more than 0.44 sec on EKG even when corrected for HR
Can present as Syncope, or sudden death due to VT
Asymmetric sympathetic innervation of the right and left heart
Prolonged Q-T Interval Syndrome
Jervell and Lange-Nielsen Syndrome
Romano-Ward Syndrome
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BB can shorten QT interval Left stellate ganglion block can transiently shorten
Q-T for acute cardiac arrhythmias Surgical Ganglionectomy is successful if the block
work EKG pre-op for children with congenital deafness or
Hx of sudden death in the family GA might trigger ventricular Dysrhythmias if not on
BB pre-op Electrical defibrillator should be available Phenytoin can shorten Q-T can be given po after
surgery
Prolonged Q-T and Anesthesia
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Malignant Hyperthermia coexisting diseases
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AT A GLANCE...
Epidemiology of MH Pathogenesis of MH 4 Different Case
Scenarios The MH Clinical
Grading Scale MH-like Anesthetic
Events
• Mimics of MH• Diseases Associated with MH
• Possibly MH-Related• Rhabdomyolysis but not MH
• Muscle Biopsy & IVCT• MHAUS, NAMHR, NMSIS
& MH Hotline• Bibliography
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“Epidemiologic barriers” in defining the true incidence of MH”
Difficulty in establishing diagnosis of MH No noninvasive diagnostic screening test
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“Epidemiologic barriers” in defining the true incidence of
MH” (cont.)
All cases are not reported to MH Registry Triggering of MH in susceptible patients may
not occur Lack of uniform criteria for MH diagnosis
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Incidence of Different Forms of MH in Relation to Type of Anesthesia
Fulminant MH Abortive MH Overall incidence (all subgroups of suspected MH included)
Total number of anesthetics 1:251,063 1:17,435 1:16,303
General anesthesia 1:221,811 1:15,404 1:14,403
Anesthesia with potent inhalation agent 1:84,488 1:6,653 1:6,167
With succinylcholine 1:61,961 1:4,506 1:4,201
Without succinylcholine 1:174,597 1:20,541 1:18,379
Anesthesia with administration of succinylcholine 1:140,006 1:8,819 1:8,297
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Pathogenesis: Key Concepts
Heterogeneous disorderGenetically transmitted with variable expression/penetrance
Can be triggered by volatile anesthetics and succinylcholine
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Hereditary - multiple genes
Several chromosomes: 19q11.2-13.2 Ryanodine (RyR1)
Release of Ca2+ stores from sarcoplasmic reticulum
17q11.2-q24 Altered sodium channel functioning
7q21.1 Dihydropyridine (DHP), voltage sensor for RyR1
1q32 CACNL1A3 gene encoding the alpha 1-subunit of the
voltage-gated DHP receptor that interacts with RyR1
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Non-specific clinical presentation
Hypercarbia Tachycardia Fever Hyperventilation Metabolic and Respiratory Acidoses Cardiovascular collapse Rhabdomyolysis
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Case One in PACU
A 13 year old boy underwent
2 hours of uncomplicated General Anesthesia.
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Case Two in OR
A 10 year-old male was given Propofol & Rocurronium to facilitate tracheal intubation. Anesthesia wascontinued with Isoflurane/N2O.
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Case Three Masseter Rigidity?
A 16 year-old male who refused spinal anesthesia for lower extremity surgery, was given Propofol and Succinylcholine (no Volatile Anesthetic gas).
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Case Four Outside
A 12 year old male collapsed after rigorous exercise.
Tobin JR, Jason DR, Nelson TE, Sambuughin. Malignant Hyperthermia and Apparent Heat Stroke N. JAMA 2001; 286(2):168-169 http://jama.ama-assn.org/issues/v286n2/ffull/jlt0711-4.html
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Process Indicator Points1. Rigidity Generalized muscular rigidity 15
Masseter spasm________________________________ 152. Muscle Breakdown Creatine Kinase >20,000 IU after succinylcholine 15
Creatine Kinase >10,000 IU with no succinylcholine 15Cola colored urine in perioperative period 10Myoglobin in urine > 60 mcg/L 5Myoglobin in serum > 170 mcg/L 5Blood/plasma/serum K> 6 mEq/L no renal ills _____ 3
3. Respiratory Acidosis PETCO2 > 55 mmHg with controlled ventilation
15 Arterial PaCO2 > 60 mmHg, controlled ventilation 15
PETCO2 > 60 mmHg with spontaneous ventilation 15
Arterial PaCO2 > 65 mmHg, spontaneous ventilation 15
Inappropriate hypercarbia, Anesthesiologist’s call 15Inappropriate tachypnea__________________________ 10
4. Temperature Increase Inappropriately rapid increase 15Inappropriately increased temperature > 38.8C_______ 10
5. Cardiac Involvement Inappropriate sinus tachycardia 3Ventricular tachycardia or fibrillation_________________ 3
6. Family History Positive family history in first degree relative 15 Positive family history, more distant relative ____ 5
7. Others Arterial base excess more negative than –8 mEq/L 10Arterial pH <7.25 10Rapid reversal of MH signs after iv dantrolene 5Positive MH family history with another indicator from the patient’s anesthetic experience other than increased CK 10Elevated CK and a family history of MH______________ 10
Larach MG, Et Al, MH Clinical Grading Scale, Anesthesiology 1994; 80:771-9
Click for larger picture
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CGS Sum and Probability of MH
Almost certine>50
Very likely35-49
Somewhat greater than
likely
20-34
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Clinical Grading Scores (CGS)
45303538 SUM
0 0 510Other
0 0 0 0Family History
15 0 0 3Cardiac
15 0 010Temperature
15 015 0Respiratory
0151515Muscle Injury
1515 0 0Rigidity
Case 4
Case 3
Case 2
Case 1
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MH-Like Anesthetic Events
< 14 years 0.000135 Myotonia Dystrophica
12 (4-19) 0.00036 Becker
5 (<16) yrs 0.0020 Duchenne
AGE at DxINCIDENCEMYOPATHY
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Differential Diagnosis
+-+++Acidosis
-+/-++Rigidity
++++++ BP
+++++++++ HR
+++++++ ETCO2
Pheochromocytoma
ThyrotoxicosisMH
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Some Mimics of MH
Adverse drug reactions Arthrogryposis Carnitine palmitoyl
transferase deficiency CNS diseases Contrast media in CSF Elevated ETCO2 with
laparoscopic cases
Cystinosis Glycogen storage
disease Lymphoma Mitochondrial disease Neuroleptic
malignant syndrome Viral myopathy William’s syndrome
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Diseases Associated with MHS
Central core disease Isolated elevation of creatine kinase King Denborough syndrome
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Possibly MH Related
Dystrophinopathy Emery Dreifuss MD Fascio-Scapulo-Humeral MD Abnormal Muscle Enzymes Ion Channel Mutations
Na, K, Cl
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Rhabdomyolysis, but NOT MH
Brody’s disease Deficient calcium adenosine triphosphatase
Mc-Ardle’s disease Myophosphorylase B deficiency
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Muscle Biopsy and IVCT
Nearly 100% sensitive
85% specific
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Anesthesia for MH Susceptible Patients
If your patient has had a muscle biopsy for MH contracture testing or is registered through the North American Malignant Hyperthermia Registry (NAMHR): Call # 888-274-7899 Complete & return report of anesthetic
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Bibliography1. Larach, MG for the North American Malignant
Hyperthermia Group. Standardization of the caffeine-halothane muscle contracture test. Anesth Analg 1989; 69:511-515
2. Laboratory diagnosis of malignant hyperpyrexia susceptibility (MHS). European MH Group. Br J Anaesth. 1985; 57(10):1038.
3. European Malignant Hyperpyrexia Group. A protocol for the investigation of malignant hyperpyrexia (MH) susceptibility. Br J Anaesth, 1984; 56: 1267-1269.
4. Allen, G, et al. The sensitivity and specificity of the caffeine-halothane contracture test. Anesthesiology 1998; 88:579-88.
5. Ording, H., et al. In-vitro contracture test for diagnosis of malignant hyperthermia following the protocol of the European MH Group: results of testing patients surviving fulminant MH and unrelated low-risk subjects. The European Malignant Hyperthermia Group. Acta Anesthesiol. Scand., 1997; 41: 955-966.
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Bibliography, cont.6. Urwyler A., et.al. Guidelines for molecular genetic
dectection of susceptibility to malignant hyperthermia. And editorial III. Br J Anaesth. 2001; 86(2): 283-7.
7. Brandt, A., et al. Screening of the ryanodine receptor gene in 105 malignant hyperthermia families: novel mutations and concordance with the in-vitro contracture test. Hum. Mol. Genet. 1999; 8: 2055-2062.
8. Brown, R., et al. A novel ryanodine receptor and genotype-phenotype correlation in a large malignant hyperthermia New Zealand Maori pedigree. Hum. Mol. Genet. 2000; 9: 1515-1524.
10. Larach, MG, et al. MH Clinical Grading Scale. Anesthesiology 1994; 80:771-9.11. Ording, H. Incidence of Malignant Hyperthermia in
Denmark. Anesth Analg 1985; 64:700-4.12. Benumof, Jonathan. Muscle Diseases. Anesthesia & Uncommon Diseases. (4/e), Philadelphia, 1998.
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Bibliography, cont..
13. Monnier N, et al. Malignant Hyperthermia susceptibility is associated with a mutation of the alpha 1 subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium channel receptor in skeletal muscle. Am J Hum Genet 1997;60(6):1316-25.
14. Tobin JR, Jason DR, Nelson TE, Sambuughin N. Malignant Hyperthermia and Apparent Heat Stroke, JAMA 2001; 286(2):168-169.
16. Larach, MG, et al. MH Clinical Grading Scale. Anesthesiology 1994; 80:771-9.
17. Dierdorf, Stephen. Anesthesia for Patients with Rare and Coexisting Diseases. Clinical Anesthesia (3/e), Philadelphia, 1996. p 461.
18. McPherson EW, Taylor CA Jr. The King Syndrome: MH, myopathy, and multiple anomalies. Am J Med Genet 8:159, 1981.
19. Loke JC, MacLennan DH. Bayesian modeling of muscle biopsy contracture testing for malignant hyperthermia susceptibility. Anesthesiology 1998;88(3):589-600.