401 likes | 669 Views
Rare diseases in everyday practice « Google anaesthesia » ?. F Veyckemans Clin univ. St Luc Brussels, Belgium. Outline. definition & queries sources of information pitfalls to prepare anaesthesia conclusion. Conflict of interest. Responsible for the website
E N D
Rare diseases in everyday practice« Google anaesthesia » ? F Veyckemans Clin univ. St Luc Brussels, Belgium
Outline • definition & queries • sources of information • pitfalls • to prepare anaesthesia • conclusion
Conflict of interest Responsible for the website tyniurl.com/m-rares Syndromes & Maladies rares en pédiatrie: anesthésie with Prof J-L Scholtes (Brussels)
Outline definition & queries sources of information pitfalls to prepare anaesthesia conclusion
What is a rare disease? < 1/2000 in the general population but depends on country population clustering clinical recruitment e.g., Duchenne microdeletion ch 22
The anaesthesiologist’s perspective care for a « rare disease » patient during a brief but often critical period of time 2) consider a disease is rare at the first time we meet it !
The anaesthetist’s queries 1) what is it ? malformative syndrome metabolic disease muscle disease 2) any increased anaesthetic risk ? 3) any special issue(s) regarding perianaesthetic care ?
Outline • definition & queries • sources of information • pitfalls • to prepare anaesthesia • conclusion
Sources of information (1) On the disease : Books • Inborn metabolic diseases, 5thed, Saudubray & coll (Springer, 2012). • Smith’s recognizable patterns of human malformations 6thed, KL Jones (Elsevier Saunders, 2006) • Atlas of Metabolic Diseases 2nded WL Nyhan & coll (Hodder Arnold, 2005)
Sources of information (1) On the disease : Internet * Google * Orphanet name : expert summary + peer reviewed *OMIM: omim.orgonline Mendelian inheritance * GARD: Genetic & Rare Diseases information center * NORD * pubmed * disease-related website: parents’ groups
Sources of information (2) Anaesthetic management of the disease Books • Anesthesia for genetic, metabolic & dysmorphic syndromes of childhood Baum & O’Flaherty (Lippincott, Williams & Wilkins, 2007) • Genetic syndromes : recognition and perioperative aspects. B Bissonnette, B Dalens .. (McGraw-Hill, 2006) • most Textbooks on Paediatric Anaesthesia contain a chapter on the most common rare diseases or syndromes
Sources of information (2) Anaesthetic management of the disease Internet: « disease and anaesthesia » *Pubmed *Google * Orphanet name emergency care * VIRTANES maladies rares de l’enfant Or discussion lists : PAC
Outline • definition & queries • sources of information • pitfalls • to prepare anaesthesia • conclusion
Different names for the same disease Treacher-Collins = Franceschetti-Klein = mandibulofacial dysostosis
Different diseases with similar name e.g., Hecht-Beals syndrome = congenital arachnodactyly with contractures CCA syndrome marfanoid syndrome Hecht syndrome = Dutch-Kentucky syndrome = trimus pseudocamptodactyly syndrome = distal arthrogryposis type 7 difficult airway
Genetics are complex one gene one protein one function one phenotype
Genetics are complex one gene other controller/inhibitor genes inactivation of chromosome one protein RNAm one function environmental factors one phenotype
Genetics are complex • one phenotype can result from different mutations/genes • mutation(s) of one gene different phenotypes • variable penetrance of some mutations • many mutations are sporadic no familial history • results often not available in time
Validity of the information ? * Google ranking of links according to a complex algoritm not to quality of data check : source of data ? Wikipedia date of last update
Validity of the information? • Case reports - often isolated cases - relative scientific value • no problem : luck ? • complication : cause-effect vs association ? poor management ? • date : old drugs ? +description of the disease from the anaesthetist’s point of view (date ?)
Validity of the information ? Ideal: case series « data from case series for a rare condition may be the best evidence a clinician can rely on » The Oxford Levels of Evidence 2, 2013 Oxford Centre for Evidence-Based Medicine
Validity of the information ? Medical progress often results in • prolonged survival • modification of evolution (gene therapy, transplantation)
Validity of the information ! • child’s parents • child’s paediatrician: personal contact ! specific information on this child
Outline definition & queries sources of information pitfalls to prepare anaesthesia conclusion
My way To summarize informations evaluate anaesthetic risk plan anaesthesia
NARCO acronym Neuromuscular Airway Respiratory Cardiovascular Others Malviya S, Voepel-Lewis T, Chiravuri SD et al. Does an objective system-based approach improve assessment of perioperative risk in children? A preliminary evaluation of the NARCO. Br J Anaesth 2011; 106: 352-6
Basic questions Neuromuscular: developmental delay ? seizures : controlled or not ? spasticity, contractures, hypotonia ? medical treatment ? Airway : difficult intubation/ventilation ? risk for regurgitation/inhalation ? obstructive sleep apnoea ? Respiratory : reactive airway ? restrictive or obstructive syndrome ? chronic lung infection ?
Basic questions Cardiovascular : congenital heart disease ? dysrythmias ? cardiomyopathy ? Others : special diet ? tolerates fasting ? previous anaesthesia ? psychological issues ?
Example : Willi-Prader syndrome - 1/10,000 - deletion of 15q11-q13 of paternal origin - mental retardation - morbid obesity - behaviour problems - hypogenitalism - epilepsy - rumination, mericism
Example : Willi-Prader syndrome Nmental retardation, epilepsy, behavioural problems hyperphagia Asmall mouth, micrognathia Rcentral & obstructive sleep apnoea, gastrooesophageal reflux, scoliosis decreased response to hypoxaemia/hypercarbia C systemic hypertension, cor pulmonale Oobese, short stature pain threshold central adrenal insufficiency during stress (60 %) spontaneous annual death rate: 3%
Example : Willi-Prader syndrome Nmental retardation, epilepsy, behavioural problems hyperphagia Asmall mouth, micrognathia Rcentral & obstructive sleep apnoea, gastrooesophageal reflux, scoliosis decreased response to hypoxaemia/hypercarbia C systemic hypertension, cor pulmonale Oobese, short stature pain threshold central adrenal insufficiency during stress (60 %) annual death rate: 3% treatment Short fasting Mask fit, intubation Night oximetry recovery Cardiac echo Difficult veins IV hydrocortisone Postop monitoring
This patient is also a child ! Do not overlook the basics : • personal history • allergies ? • haemostasis ? • upper airway: infection ? difficult airway? • passive smoking ? • easy veins ? • BP, auscultation
Outline • definition & queries • sources of information • pitfalls • to prepare anaesthesia • conclusion
Conclusion (1) • check the name • seek information : disease / anaesthesia - textbooks - internet : time of update ? • Orphanet Orphanaesthesia ? • standard but focused preop examination • summarize with NARCO
Conclusion (2) • a few keys to help manage a child with a rare disease • increase interest in rare diseases • suggestion: creation of a national/APA registry of anaesthetics for patients with a rare disease source of information
APRICOT AnaesthesiaPractice In ChildrenObservationalTrial European prospective multicenterobservationalstudy: Epidemiology of severecriticalevents JOIN THE NETWORK research@esahq.org esa.apricot@gmail.com