The ‘‘single airway’’ concept  The upper respiratory tract -nose and paranasal sinuses- has the same mucosal lining as the lower airways  Both compartments.

Slides:



Advertisements
Similar presentations
Fig 1 Anatomy.
Advertisements

Nasal Polyps Dr. Vishal Sharma.
Perioperative Management of Endoscopic Sinus Surgery Chad McCormick, MD, FAAOA.
Chronic RhinoSinusitis- State of the Art
Rhinosinusitis Sinusitis Sinusitis affects 31 million Americans annually. Chronic sinusitis is defined as unrelenting symptoms >12 weeks in duration.
Nursing Care of Clients with Upper Respiratory Disorders.
ADVANCES IN TREATMENT OF SINUS DISEASE ADVANCES IN TREATMENT OF SINUS DISEASE James V. Zirul, D.O. Peninsula Ear, Nose & Throat Clinic, Inc. Kenai, Alaska.
C A SHINKWIN BON SECOURS GP STUDY DAY 28 JANUARY, 2012.
Sniffing out the problem Jonathan Hern. Commissioning Guide for Chronic Rhinosinusitis ENTUK and RCS Based on European position paper on sinusitis Guidance.
Bronchiectasis. DEFINITION OF BRONCHIECTASIS It is a chronic and necrotizing condition of bronchi and bronchioles leading to their abnormal dilatations.
PEDIATRIC RHINOSINUSITIS DANIEL W. TODD, MD, FACS MIDWEST ENT.
Cystic Fibrosis Gina Brandl, RN BSN Nursing Instructor, Pediatrics.
Nasal Polyposis.
Lesson 4 Care and Problems of the Respiratory System Respiratory system problems can affect the functioning of other body systems. Imagine not being able.
Tiffany Rimmer.  CF is the most common lethal autosomal recessive genetic disease in Caucasians.  It affects over 30,000 individuals in the United States.
Pathogenesis AND treatment of Chronic Rhinosinusitis 1.
Chronic Sinusitis.
1 RETROSPECTIVE EVALUATION OF THE PATIENTS WITH CYSTIC FIBROSIS DR.LALE PULAT SEREN ZEYNEP KAMİL MATERNITY AND CHILDREN’S TRAINING AND RESEARCH HOSPITAL.
Rhino-sinusitis Done By : Dina Shamaileh.
ACUTE & CHRONIC (RHINO-) “SINUSITIS”. Classification by duration of symptoms –ACUTE – lasting up to 4 weeks, with total resolution of symptoms –SUBACUTE.
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.
Prepared by Dr. Muaid I.Aziz FICMS.  It’s a group of disorders characterized by inflammation of the mucosa of the nose & pns.
Objectives Upon completion of the lecture, students should be able to:  Define middle ear infection  Know the classification of otitis media (OM). 
Dr Abdalla Elfateh Ibrahim Consultant and assistant Professor Of Pulmonary Medicine.
Bronchiectasis Sami ur Rahman Roll No: Overview Definition Etiology Pathology Clinical Presentation Diagnosis Treatment.
Bronchiectasis SS Visser, Pulmonology Internal Medicine UP.
Diseases of the paranasal sinuses Ehab ZAYYAN, MD, PhD
Nasal Polyps By Alex Pearce-Smith.
Clinical physiology—ENT: Prof James Ker MBChB, MMED, MRCP, FRCP, PhD, FESC, FACC, L.Akad.SA.
Respiratory Disorders. Asthma Condition where smooth muscle that lines the airways contracts, making it difficult to breathe. –Allergy-induced Asthma.
Approach to bronchiectasis
RHINOSINUSITIS DANIEL W. TODD, M.D. MIDWEST ENT FORM AND FUNCTION FORM (ANATOMY)FUNCTION (PHYSIOLOGY)
Cystic Fibrosis By: Morgan. Definition Cystic fibrosis is a thick mucus that clogs the air ways and tends to cause lung diseases. A diseases common among.
The Medical Management of Infective & Allergic Rhinitis Joe Marais FRCS(ORL) Hillingdon Hospital, Northwick Park Hospital, Bishops Wood.
Dr Jennifer Price VTS ST2 1 st May  Otitis media with effusion (OME), also known as 'glue ear', is a condition characterized by a collection of.
Primary Ciliary Dyskinesia Assoc. Prof. Bulent KARADAG Marmara Uni. Faculty of Medicine Div. of Pediatric Pulmonology ISTANBUL-TURKEY.
Chronic Sinusitis Robert Walsh. Sinus Anatomy  The Paranasal sinuses are paired hollow spaces surrounding the nasal cavity within the facial bones 
Lesson 4 Care and Problems of the Respiratory System Respiratory system problems can affect the functioning of other body systems. Imagine not being able.
Clinical manifestation and diagnosis of bronchiectasis Aleš Rozman University Clinic of Respiratory Diseases and Allergy, GOLNIK, Slovenia Portorož – 9th.
7.3 – Respiratory Health Respiratory health problems can be identified as conditions that affect either the upper respiratory tract, or the lower respiratory.
MARIAM MUKHTAR CASE PRESENTATION. CASE: 24 year old male patient k/C of asthma and bronchiectasis. c/o: worsening SOB and C/P x 1m.
Rhinosinusitis Dr. Abdullah S. Al Yousef. Allergic Rhinitis Definition : An inflammatory disorder of the nose which occurs when the membranes lining the.
The Role of Cilia in Development and Disease The Role of Cilia in Development and Disease Produced by Gui Ming jie & Li Jing Directed by Pro. Yin.
Objectives Review the causes of cystic fibrosis (CF) Describe the symptoms and laboratory findings in CF Review current and emerging CF treatments Review.
Linda S. Williams / Paula D. Hopper Copyright © F.A. Davis Company Understanding Medical Surgical Nursing, 4th Edition Chapter 30 Nursing Care of.
Schematic diagram of motion of a single cilium during the rapid forward beat and the slower recovery phase.
SINUSITIS & ITS COMPLICATIONS
Upper Respiratory Tract Disorder Lecture 2 12/14/20151.
Cystic Fibrosis.
Sinusitis. n Inflammation or infection of the mucous membranes of nose & sinuses n Rhinosinusitis –rhino refers to nose and nasal passages n Acute n Chronic.
COPD ) ) Chronic Obstructive Pulmonary Disease. Introduction n COPD is a preventable and treatable disease with some significant extrapulmonary effects.
Management of Patients With Chronic Pulmonary Disease
Sinusitis Dr.Emamzadegan Ped.Cardiologist. Sinusitis Sinusitis is a common illness of childhood and adolescence.
Epidemiology of nasal polyp Dr T Balasubramanian.
 Wheezing illnesses other than asthma in children.
PARANASAL MUCOCELE IN CYSTIC FIBROSIS CHILDREN °Di Cicco M. MD *Costantini D.MD. *Colombo C.MD °Otorhinolaryngology Dept., *Pediatrics Dept. CF Centre,
Depart. Of Pulmonology & Critical Care Medicine R4 백승숙 Barbara J. Turner, Sankey Williams, Darren Taichman.
J R Hurst Thorax : Depart. Of Pulmonology R3 백승숙.
Depart. Of pulmonology R4 백승숙
An Inflammatory condition involving the paranasal sinuses and linings of the nasal passages that lasts 12 week or longer This diagnosis requires objective.
Cystic fibrosis. Etiology and epidemiology Cystic fibrosis (CF) is an autosomal recessive disorder that is the most common life limiting genetic disease.
Evaluation of combined middle and inferior meatal antrostomies for endonasal eradication of severe maxillary sinusitis Adel Said El-Antably.
Conditions of the Respiratory System
DR . ABDUL HAMEED AL QASEER
Chronic sinusitis Prof. Ehab Taha Yaseen.
ENT & AUDIOLOGY REFERRALS
BENAZIR BHUTTO HOSPITAL
Chronic sinusitis Journal of Allergy and Clinical Immunology
Presentation transcript:

The ‘‘single airway’’ concept  The upper respiratory tract -nose and paranasal sinuses- has the same mucosal lining as the lower airways  Both compartments are involved together in health and disease  In asthma, allergic rhinitis and nasal polyposis  Similarly useful in chronic infective respiratory conditions

Mucociliary clearance - Important first-line defence of both upper & lower respiratory tracts - Trap inhaled matter and propel it to the nasopharynx  Impaired sinonasal clearance  Stasis of secretions  Prone to bacterial infection  Chronic rhinosinusitis  Other important host defences - Immunoglobulins, defensins - Aantibacterial components of the mucus such as lysozyme

 Same aetiology and pathophysiology  Sinonasal disease may directly influence the bronchial condition  Rarely considered together & Little literature on the treatment of sinonasal disease in bronchiectasis This article  Review sinonasal disease in bronchiectasis and cystic fibrosis  Addresses the possible interactions between the health and disease of the upper and lower airways Bronchiectasis and cystic fibrosis Sinonasal disease

 Rhinosinusitis - Inflammation of the nose and paranasal sinuses - Nasal obstruction/congestion or anterior/posterior rhinorrhoea - Anosmia and facial pain or pressure  Acute rhinosinusitis ; Sx. < 12 weeks Nasal polyposis  Chronic rhinosinusitis ; Nasal polyposis - Chronic inflammatory disease of the nose and sinus mucosa - Frequently associated with asthma, cystic fibrosis (CF), primary ciliary dyskinesia (PCD) and aspirin sensitivity

 2.7% 6.6%  2.7% and 6.6% of the population have chronic rhinosinusitis  Increased incidence in patients with chronic inflammatory lower respiratory disease  Chronic rhinosinusitis can impact heavily on quality of life with significant impairments on health status instruments  Patients with chronic rhinosinusitis had more general body pain and worse social functioning than those with COPD or heart failure -The health impact of chronic sinusitis in patients seeking otolaryngologic care -The health impact of chronic sinusitis in patients seeking otolaryngologic care Otolaryngol Head Neck Surg 1995 Otolaryngol Head Neck Surg 1995

 Abnormal dilation of the bronchi due to the loss of elastic and muscular components of the wall due to destruction by enzymes such as collagenase and elastase from neutrophils - Excess mucus production - Recurrent lower respiratory tract infections  End result of several different aetiologies  It is almost universal, and often more severe, when the sinusitis and bronchiectasis share a common aetiology

 Autosomal recessive condition whereby ciliary motility is absent or severely impaired leading to sinusitis, otitis media, glue ear, chronic bronchitis, bronchiectasis and male infertility  Kartagener’s syndrome ; association of situs inversus characterises  Patients have congested noses from birth and often have difficulty breast feeding due to the inability to nose breathe  Need for cilia investigation

 Characterised by bronchiectasis, chronic rhinosinusistis and male infertility  Ciliary function is found to be normal and clearance is impaired because the mucus is viscous  Association with mercury poisoning in childhood from teething powders and treatment of worm infections  Diagnosis is made on exclusion of CF and PCD

 Autosomal recessive condition characterised by a defect in the CF transmembrane conductance regulator gene product that leads to abnormalities of ion flux at the epithelial surface  The increased sodium absorption leads to periciliary liquid depletion and abnormal mucus movement  Clinically, patients progress to chronic respiratory failure caused by bacterial infections and have pancreatic insufficiency

 Nasal mucociliary clearance ; small saccharin particle is placed on the medial side of the inferior turbinate and the time taken to experience the taste recorded, with abnormal values typically > 20 min - Use of colloid particles labelled with technetium-99  Nasal brush biopsy - Structure and function of the cilia is assessed following a - Cyto logy brush; scrape epithelial cells from the inferior turbinate  Expired nitric oxide levels - Useful in the assessment of a patient with bronchiectasis - Screening tool for PCD Assessment of mucociliary clearance

 Review of the symptoms an assessment of their severity  Review of the symptoms & an assessment of their severity - The amount and type of discharge - Any facial pain or smell disturbance - The degree of nasal obstruction  Rhinomanometry  Anterior rhinoscopy & Endoscopy  Radiography of the sinuses  CT Assessment of upper airway Failure of treatment Failure of treatment Preoperatively Preoperatively For complications For complications

 Japanese study  Japanese study ; 45% of patients with idiopathic bronchiectasis  UK study  UK study ; 84% of patients with idiopathic bronchiectasis 50% of those with postinfective bronchiectasis  Anterior and posterior rhinorrhoea, anosmia and nasal obstruction  Nasal polyps occur in up to 40%  S. aureus, CNS, GNB & Anaerobic  Universal in PCD and Young’s syndrome

 Almost patient with CF has nasal and paranasal sinus disease  < 10% of patients with CF typically report significant symptoms  S. aureus, H. influenzae prevalent in the younger age group  P. aeruginosa important in older patients  Anaerobes and fungi (1/3 of CF patients)  The different sinonasal manifestations and severity of CF  No associations  Complications of sinonasal disease (eg, mucoceles) in CF  Much rarer than in the general population

 Initial therapy should be medical with the aim to relieve symptoms, improve quality of life and avoid disease complications  Chronic rhinosinusitis often responds incompletely to treatment, which is usually continued long term

 Improved drainage › Saline irrigation ; clear secretions and nasal crustings › Saline nasal spray (eg, Sterimar) or Douching (eg, Sinu-rinse) › Topical decongestants  Steroids Topical nasal steroids › Improvements in both symptoms and objective measures › Reduce nasal polyp size and symptoms Medical treatment

 Antibiotics  Topical ointments (eg, Bactroban, Naseptin)Macrolides › Reduce inflammatory cytokines(eg, IL-8, TNF-α), inflammatory cell recruitment and free radical production › Improve ciliary motility and reduce biofilm production › Not studied in patients with CF or bronchiectasis  Other agents › Topical mucolytic, N-acetylcysteine › Antileukotrienes, antihistamines

 Surgery › Performed endoscopically with the aim of improving drainage Endoscopic sinus surgery Endoscopic sinus surgery - Reserved for patients who do not respond to medical treatment - Well tolerated in patients with CF Surgical treatment

 Sinonasal disease › Significant morbidity in patients with chronic respiratory disease › It can also significantly impact on lower respiratory health › It should not be considered in isolation  Asthma, Children with CF  Bronchiectasis › Migration of organisms from the upper respiratory tract › Acting as a ‘‘sump’’ for reinfection › Early detection of colonization and aggressive management › P. aeruginosa eradication protocols

“Single airway” model Common aetiology and pathophysiology of sinonasal and respiratory disease Improve lower respiratory health Improve lower respiratory health Reduce infection & inflammation Reduce infection & inflammation in the bronchiectatic airway in the bronchiectatic airway Appreciation & treatment of of Concomitant sinonasal dis.