Cystic fibrosis

Description

Paediatrics (Respiratory) Mind Map on Cystic fibrosis, created by v.djabatey on 06/01/2014.
v.djabatey
Mind Map by v.djabatey, updated more than 1 year ago
v.djabatey
Created by v.djabatey almost 11 years ago
90
2

Resource summary

Cystic fibrosis
  1. clinical features
    1. newborn
      1. diagnosed through newborn screening
      2. infancy
        1. meconium ileus
          1. newborn period
          2. prolonged neonatal jaundice
            1. failure to thrive
              1. recurrent chest infections
                1. malabsorption, steatorrhoea
                2. young child
                  1. bronchiectasis
                    1. rectal prolapse
                      1. nasal polyp
                        1. sinusitis
                        2. older child and adolescent
                          1. allergic bronchopulmonary aspergillosis (ABPA)
                            1. diabetes mellitus
                              1. cirrhosis & portal hypertension
                                1. distal intestinal obstruction (DIOS, meconium ileus equivalent)
                                  1. pneumothorax or recurrent haemoptysis
                                    1. sterility in males
                                  2. Diagnosis
                                    1. sweat test
                                      1. essential diag procedure
                                        1. to sig elevation in [Cl-] in sweat
                                          1. normal kids= 10-40 mmol/L
                                            1. CF= 60-120 mmol/L
                                            2. stimulate sweating
                                              1. by pilocarpine iontophoresis
                                                1. collect sweat
                                                  1. into special capillary tube
                                                    1. absorb it onto weighed filter paper
                                                  2. diag error common if not enough sweat collected
                                                  3. gene abnormalities in CFTR protein
                                                    1. detect to confirm diag
                                                      1. if child homozygote for 2 IDed mutations, then has CF
                                                    2. management
                                                      1. MDT approach
                                                        1. paediatricians
                                                          1. physiotherapists
                                                            1. dieticians
                                                              1. specialist nurses
                                                                1. primary care team
                                                                  1. pt & fam, teachers
                                                                  2. at least annual review at CF centre
                                                                    1. aims of therapy
                                                                      1. prevent progression of lung disease
                                                                        1. maintain adequate nutrition & growth
                                                                        2. Respiratory management
                                                                        Show full summary Hide full summary

                                                                        Similar

                                                                        Upper respiratory tract infection (URTI)
                                                                        v.djabatey
                                                                        Bronchiolitis
                                                                        v.djabatey
                                                                        Pneumonia
                                                                        v.djabatey
                                                                        Laryngeal & tracheal infections
                                                                        v.djabatey
                                                                        Bronchitis
                                                                        v.djabatey
                                                                        Finger clubbing
                                                                        v.djabatey
                                                                        Cystic fibrosis- epidem, pathophysiology, clinical features
                                                                        v.djabatey
                                                                        Respiratory System
                                                                        Addeana
                                                                        Paediatrics Respiratory
                                                                        Liam Musselbrook
                                                                        Chronic Respiratory Conditions
                                                                        Kirsty Jayne Buckley
                                                                        Respiratory System 2nd Year PMU Anatomy
                                                                        Med Student