A Sticky (and Thick) Situation
Tiny lungs, Big Problems
CF Around the World
MUCUS MAYHEM
100

What are the "Gold-Standard" for diagnosing CF?

Sweat Chloride Test

100

Persistent coughing and this breathing sound are common in children with CF.

Wheezing

100

Approximately this fraction of Caucasians are carriers of CF.

What is 1 in 25?

200

The symptoms of CF (Name at LEAST 4)

Wheezing, coughing, chloride in sweat, frequent lung infections, digestive complications 

200

These frequent lung issues often require repeated antibiotic treatment.

What are recurrent respiratory infections?

200

Name two organ systems affected by cystic fibrosis.

What are....

300

Describe the difference between a normal and mutated CFTR protein.

What is normal salt/water regulation vs. irregular production of thick mucus?

300

This neonatal intestinal obstruction is often the first sign of CF.

What is meconium ileus?

300

Explain why CF is considered a multisystem disease.

What is CFTR is expressed in multiple organs?

300

Compare acute versus chronic treatment strategies for cystic fibrosis in pediatric patients.

What is acute treatment using IV antibiotics and oxygen to manage exacerbations, while chronic treatment involves lifelong airway clearance, inhaled medications, nutritional support, and CFTR modulators? 

400

Match mutation classes (no protein), (defective processing), (defective gating), (defective conduction), (accelerated turnover),  (reduced quantity).

Good Luck

What are: Class I (no protein), II (defective processing), III (defective gating), IV (defective conduction), V (reduced quantity), VI (accelerated turnover)?

400

Explain how CF leads to failure to thrive in pediatric patients.

What is pancreatic insufficiency causing malabsorption of nutrients? 

400

What has CF, being an autosomal recessive disease with a high carrier frequency resulted in?

What is newborn screening for early detection?

400

These resources help improve adherence to therapy, mental health, and overall outcomes in patients with cystic fibrosis.

What are support resources?