Prevalence of Cystic Fibrosis (CF) carriers given CF-related conditions
What CF-related conditions do the patients have?
All CF-related conditions
Abdominal pain
Abnormal liver serum enzyme levels
Acute Bronchitis
Acute Pancreatitis
Acute Sinusitis
Ascites
Aspergillosis associated disease
Asthma
Bronchiectasis
Cachexia and Adult Failure to thrive
Cancer of other GI organs; peritoneum
Cholelithiasis
Chronic Bronchitis
Chronic Hepatitis
Chronic Pancreatitis
Chronic Sinusitis
Cirrhosis
Colon Cancer
Congenital cystic lung
Congenital pneumonia
Constipation
Cyst/pseudocyst of pancreas
Dehydration
Diarrhea
Eosinophilic Esophagitis
Failure to thrive (child)
Fecal impaction
Feeding difficulties and mismanagement
Fluid and electrolyte disorders
Gastroesophageal reflux disease (GERD)
Hemoptysis
Hypertrophic osteoarthropathy/clubbing
Intestinal atresia
Intestinal Malabsorption
Intestinal obstruction
Jaundice (not of newborn)
Lack of Expected Normal Development
Male infertility
Meconium obstruction in fetus or newborn
Meconium peritonitis
Nasal Polyposis
Nausea or Vomiting
Neonatal jaundice
Nephrolithiasis
Nontuberculous Mycobacterial Infection
Osteopenia
Osteoporosis
Other Pancreatic Disorders
Pancreatic Cancer
Pancreatic Steatorrhea
Personal history of recurrent pneumonia
Pneumonia
Pseudomonas Infections
Respiratory Failure
Respiratory Failure of Newborn
Scoliosis
Secondary Diabetes
Short stature
Stomach Cancer
Type I Diabetes
Upper Respiratory Infection-Unspecified
Venous thromboembolism
How should the prevalence be calculated?
Individual: Patients have each of the diagnoses
Intersection: Patients must have all the diagnoses
Union: Patients must have at least one of the diagnoses
What is the sex of the possible carriers?
Sex not specified
Male
Female
What is the age of the possible carriers?
Age not specified
[0,18)
[18,40)
40+
Which CF–related condition has prompted multiple clinical visits for this patient?
Do not consider multiple visits for a given condition
Abdominal pain
Abnormal liver serum enzyme levels
Acute Bronchitis
Acute Pancreatitis
Acute Sinusitis
Ascites
Aspergillosis associated disease
Asthma
Bronchiectasis
Cachexia and Adult Failure to thrive
Cancer of other GI organs; peritoneum
Cholelithiasis
Chronic Bronchitis
Chronic Hepatitis
Chronic Pancreatitis
Chronic Sinusitis
Constipation
Dehydration
Diarrhea
Eosinophilic Esophagitis
Failure to thrive (child)
Fecal impaction
Feeding difficulties and mismanagement
Fluid and electrolyte disorders
Gastroesophageal reflux disease (GERD)
Hemoptysis
Intestinal Malabsorption
Intestinal obstruction
Jaundice (not of newborn)
Lack of Expected Normal Development
Nasal Polyposis
Nausea or Vomiting
Neonatal jaundice
Nephrolithiasis
Nontuberculous Mycobacterial Infection
Other Pancreatic Disorders
Pancreatic Steatorrhea
Pneumonia
Pseudomonas Infections
Respiratory Failure
Upper Respiratory Infection-Unspecified
Venous thromboembolism
How many clinical visits has the patient had for the specifiedCF–related condition?
At least 1 visit
At least 2 visits
At least 3 visits
What is the population prevalence of being a CF carrier?