Thinking lean: implementing DMAIC methods to improve efficiency within a cystic fibrosis clinic.
Chad Smith1, Suzanne Wood, Bradley Beauvais
1Army-Baylor University, Bethesda, Maryland, USA.
Lean methods significantly reduced patient visit times in cystic fibrosis (CF) clinics. This optimization improved efficiency, increasing clinic capacity and annual revenue without additional costs.
Area of Science:
- Healthcare Management
- Clinical Operations
- Process Improvement
Background:
- Coordinating care for cystic fibrosis (CF) patients with multiple specialists is complex.
- Inefficiencies in CF clinic structures hinder optimal resource utilization.
- Frequent clinical encounters are crucial for superior CF outcomes but can be time-consuming.
Purpose of the Study:
- To apply Lean methods to reduce patient visit lead time in a CF clinic.
- To decrease non-value-added patient time without altering provider care duration.
- To assess if reducing process variation can improve clinic efficiency.
Main Methods:
- Implementation of Lean methodologies within a CF clinic setting.
- Analysis of patient visit durations before and after process changes.
- Measurement of non-value-added time and overall lead time.
Main Results:
- Patient visit completion within 60 minutes increased from 19.3% to 41.5%.
- Mean and median patient visit times decreased by 10 minutes.
- Clinic capacity increased by 500 patient visits annually, generating over $165,000 in revenue.
Conclusions:
- Lean methods effectively reduce lead time and non-value-added time in CF clinics.
- Process optimization can significantly improve clinic efficiency and financial performance.
- Reducing variation in clinical practice enhances patient flow and resource utilization.
More Related Videos
06:14Optimized LC-MS/MS Method for the High-throughput Analysis of Clinical Samples of Ivacaftor, Its Major Metabolites, and Lumacaftor in Biological Fluids of Cystic Fibrosis Patients
Published on: October 15, 2017
06:57The WinCF Model - An Inexpensive and Tractable Microcosm of a Mucus Plugged Bronchiole to Study the Microbiology of Lung Infections
Published on: May 8, 2017
Related Concept Videos
Cystic Fibrosis: Management
Sinus disease and chronic sinusitis...
Methods of Documentation VI: Case Management Model
For example, a patient with a chronic illness...
Chronic Obstructive Pulmonary Disease-V: Nursing Management
Assessment
Chronic Obstructive Pulmonary Disease-V: Management
Smoking Cessation
Chronic Pancreatitis II: Collaborative Care
Assessment:
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
