RESPIRATORY PAEDIATRICS Dr Pamela Lewis. 6yr Male Emergency Department Sudden onset wheeze and DIB Preceding URTI Atopic Interval symptoms.

Slides:



Advertisements
Similar presentations
Chronic Productive Cough Dr. Miao Shang Su. Present History - A 5-year-old girl come to your clinic for the first time. Her mother reports that the child.
Advertisements

Cystic Fibrosis BY. MERCEDES.
EVIDENCE BASED GUIDELINE FOR MANAGEMENT OF CHILDREN PRESENTING WITH ACUTE BREATHING DIFFICULTY Produced by the Paediatric Accident and Emergency Research.
Respiratory Care in Children Better Care for Better Outcomes Dr Duncan Keeley GP Thame Thames Valley Strategic Clinical Network.
Respiratory illness in childhood
The patient with shortness of breath. Differential diagnosis Asthma Asthma COPD COPD Pneumonia Pneumonia Heart failure Heart failure PE PE Other Other.
Dr Angela Jenkins ST3 Anaesthetics 10 th September 2008.
Common Paediatric Emergency Referrals Mark Anderson Consultant Paediatrician Great North Children’s Hospital.
Acute Respiratory Diseases in the Tropics: diagnosis and treatment protocols for resource poor areas of sub-Saharan Africa Taste of Tropical Medicine Bill.
Bronchiolitis Dr M Tariq Consultant Paediatrician with Respiratory Interest.
TB Presentation for Healthcare Students
18/10/ Mostafavi SN. MD Pediatric infectious disease departement Isfahan University of Medical Science 18/10/13902.
RESPIRATORY PAEDIATRICS Dr Pamela Lewis. OBJECTIVES History – Key points Examination Common respiratory problems in children.
Respiratory approach.
Cystic fibrosis. Cystic fibrosis (CF) is an autosomal recessive genetic disorder that affects most critically the lungs, and also the pancreas, liver,
Dr. Simon Benson GP Specialist Trainee. Introduction Diagnosis of pneumonia in children with wheeze is difficult Limited data exists regarding predictors.
Tiffany Rimmer.  CF is the most common lethal autosomal recessive genetic disease in Caucasians.  It affects over 30,000 individuals in the United States.
1 RETROSPECTIVE EVALUATION OF THE PATIENTS WITH CYSTIC FIBROSIS DR.LALE PULAT SEREN ZEYNEP KAMİL MATERNITY AND CHILDREN’S TRAINING AND RESEARCH HOSPITAL.
Berkeley Fial Michaela McNiff.  Someone gets Cystic Fibrosis when they inherit two mutated genes – one from each parent.  The CF gene is on chromosome.
By: Ruth Maureen Riggie
Lower Respiratory Tract Infections in Children Abdelaziz Elamin Professor of Child Health University of Khartoum Sudan.
By Taliyah and Selina. Cystic Fibrosis CF Mucoviscidosis.
The Child with Cystic Fibrosis Lydia Burland. Learning Outcomes By the end of the session you should;  Know the basic physiology underlying CF  Recognise.
Symptoms In newborns: – Delayed growth – Failure to gain weight normally during childhood – No bowel movements in first 24 to 48 hours of life – Salty-tasting.
British Guideline on the Management of Asthma. Aims Review of current SIGN/BTS guidelines –Diagnosing Asthma –Stepwise management of Asthma –Managing.
Unit 5: IPT Isoniazid TB Preventive Therapy
Respiratory Disease In Childhood
Clinical Pathological Conference Kartikya Ahuja, M.D. Resident Physician Department of Medicine NYU School of Medicine July 20 th, 2007.
Dr A.J.France © A.J.France Objectives  Define the range of conditions  Recognise the common clinical presentations  Understand the significance.
Acute Respiratory Disorders in Children
THEME: PULMONARY TUBERCULOSIS ESSAY Kazakh National medical university named after S.D. Asfendiyarov Department of foreign languages Made by: Kalymzhan.
T. Cymes Stage 3 student doctor University of Cambridge.
Tuberculosis Egan’s Chapter 22. Mosby items and derived items © 2009 by Mosby, Inc., an affiliate of Elsevier Inc. 2 Tuberculosis (TB) The incidence of.
Cystic fibrosis is an inherited disease that causes thick, sticky mucus to build up in the lungs and digestive tract.
1 Respiratory Emergencies. 2 Objectives Differentiate between the categories of respiratory dysfunction Describe the assessment of a child with respiratory.
Chapter 4 Cough or difficult breathing Case III. Case study: Mary is an 8 year old girl with cough and weight loss for some weeks.
NYU Medical Grand Rounds Clinical Vignette Verity Schaye, MD PGY-3 September 15, 2010 U NITED S TATES D EPARTMENT OF V ETERANS A FFAIRS.
Pneumonia Name Dr J Mackintosh & Dr J Thurlow Date 18/11/2014
MAJOR EVENTS AND EVOLUTION IN CYSTIC FIBROSIS PATIENTS Author: Alexandra Martin Coordinator: Dr. Reka Borka Balas University of Medicine and Pharmacy Târgu-
Cystic Fibrosis.
Childhood Respiratory Conditions
Exacerbations. Exacerbations An exacerbation of COPD is an acute event characterized by a worsening of the patient’s respiratory symptoms that is beyond.
The Child with Stridor 1: Acute Stridor
Phase 3a Rupy Chana and Alex Cross The Peer Teaching Society is not liable for false or misleading information…
Bronchiolitis Abdullah M. Al-Olayan MBBS, SBP, ABP. Assistant Professor of Pediatrics. Pediatric Pulmonologist.
Management of Patients With Chronic Pulmonary Disease
Cystic Fibrosis and Termination of Pregnancy Jalandria Gurley, MS, FNP-BC Texas Woman’s University.
CHILDHOOD ASTHMA IN PRIMARY CARE Dr Naushin Hossain GPST1.
The Respiratory System Paediatrics OSCE Revision Elizabeth Evans.
BY: TERESA KRASZEWSKI CYSTIC FIBROSIS. BACKGROUND AND HISTORY Late 16th century babies who had “salty skin” when kissed were likely to die 1938 Dr. Dorothy.
Assessment in a systematic way
Case Discussion 2 - TB IN CHILDREN by Dr. Jeyaseelan P. Nachiappan & Dr. Suryati Adnan 1 Picture of CPG Cover.
BRONCHIOLITIS Dr Jonny Taitz, FRACP Geschn Paediatrician Sept 2003.
Cystic Fibrosis By:YaYPhineas(Edward). What is Cystic Fibrosis? A genetic disorder that affects your digestive and respiratory system You inherit a defective.
Pneumonia Infection and inflammation of the lungs Alveoli fill with fluids and mucus resulting in coughing and difficulty breathing Treatment: medication.
Chapter 4 Cough or difficult breathing Case III
Tuberculosis for Addiction Counselors
Respiratory disorders
Evaluation and Treatment of Children with Bronchiolitis in the Emergency Department Suspected bronchiolitis: Otherwise healthy child < 24 months of age.
Cystic Fibrosis By: Tamaryn Cortes.
Cystic fibrosis BY: NATALIE ALZAGA STEPHANY GODINEZ STEPHANY TORO
Asthma/ Wheeze and children
Evaluation and Treatment of Children with Bronchiolitis in the Emergency Department Suspected bronchiolitis: Otherwise healthy child < 24 months of age.
Paula Chilvers GPST2 November 2017
CASE HISTORY Dr. Zahoor.
Disorders of the Respiratory System
Unit 3 Notes: Respiratory Disorders
Respiratory disorders
Respiratory illness in children Assessment and management of acute episodes Jeremy Hull, CHOX Oxford Children’s Hospital.
Chapter 4 Cough or difficult breathing Case III
Presentation transcript:

RESPIRATORY PAEDIATRICS Dr Pamela Lewis

6yr Male Emergency Department Sudden onset wheeze and DIB Preceding URTI Atopic Interval symptoms

Acute Asthma Assessment of severity Talking Respiratory rate Accessory muscle use Heart rate Oxygen saturations Peak Flow

Acute Asthma Management ABC and Oxygen B2 Agonist (LVS or Neb) Steroids (oral prednisolone/iv hydrocortisone) Ipratropium bromide neb Aminphyline/iv salbutamol Magnesium sulphate

Asthma- Chronic Management Interval symptoms and exacerbations Adherence Inhaler and spacer technique Growth Examination PF FEV1/FVC Medication BTS stepwise approach

3 month Female Emergency Department Cough, coryza, fever and poor feeding Preterm 25/40, oxygen until 6 wks of age Parental smoking Respiratory distress with bilateral crackles and wheeze

Bronchiolitis assessment Feeding (<50%) RR (>70) Nasal flare, grunting,recession Oxygen sats <92% History of apnoeas

Bronchiolitis Management Oxygen Fluids Consider blood investigations if diagnosis in doubt or severe CXR not routine In deterioration CPAP/IPPV Palivixumab prophylaxis for risk groups

10 Yr Male Emergency Department 2 days cough, fever> 39, abdominal pain and rigors No prior respiratory history HR 130 Refill 3 seconds BP 100/60 RR 36 dull to PN right base with crackles

Pneumonia Management ABC and Oxygen Fluids Antibiotics CXR BC FBC Electrolytes Sputum culture Complications Empyema, SIADH

4 yr Female Emergency Department Temperature 40, marked respiratory distress, soft stridor, drooling Unvaccinated

Epiglotitis SHOUT FOR HELP Senior anaesthetist, paediatrician, ENT Rapid sequence induction of anaesthesia Antibiotics ceftriaxone (Hib)

Childrens Outpatients 6 month Male Recent arrival in UK ( Europe) FTT Recent right upper lobe pneumonia Loose stools, good appetite Examination, weight < 0.4 th (BW 50 th ) cough and mild i.c recession

Cystic Fibrosis AR chromosome 7, CFTR defect,DF508 UK 1:2500, gene carrier 1:25 Multi organ involvement Respiratory: decreased mucocilliary clearance, diminished local defences and increased bacterial adherence, progressive loss of respiratory function

CF Diagnosis UK screening programme Heel Test at 6 days IRT Genetic testing CF mutations Sweat test Chloride > 60 (sodium < Chloride)

CF Management Multi disciplinary Infections prophylactic and treatment Nutrition Physiotherapy Psychology Screening for complications: liver, diabetes

Childrens Outpatients 3yr Female Refugee from Somalia Protracted cough, fevers, FTT Limited Family history no vaccination history CXR hilar lymphadenopathy and RUL collapse

TB Diagnosis Latent v Active TB Mantoux 6mm positive in those without prior BCG, >15mm positive in those with BCG Consider Gamma Interferon testing Sputum DON’T FORGET HIV

Treatment TB 6 month regime 2 months Rifampicin, isoniazid, pyrayinamide and ethambutol then 4 months rifampicin and isoniazid DOTS Public health and contact tracing