Chronic neuropathic cough represents a distinct pathophysiological entity separate from common causes of chronic cough. Understanding its unique mechanisms is crucial for proper diagnosis and treatment, particularly as novel therapeutic options emerge.
○ Inflammatory-mediated bronchial hyperresponsiveness
○ Reversible airway obstruction
○ Type 2 inflammation
○ Responds to bronchodilators and anti-inflammatory therapy
○ Upper airway inflammation
○ Post-nasal drip
○ Mechanical stimulation of cough receptors
○ Responds to antihistamines and nasal steroids
○ Direct acid irritation
○ Microaspiration
○ Vagal reflex mechanisms
○ Responds to acid suppression
○ Mechanical irritation
○ Inflammatory response
○ Mucus hypersecretion
○ Anatomical abnormalities
○ Hypersensitivity of neural pathways
○ Absence of significant inflammation
○ Normal imaging studies
○ Poor response to conventional treatments
○ Central sensitization
○ Peripheral nerve dysfunction
○ Altered sensory processing
○ Neural plasticity
○ ATP-gated ion channel
○ Expression on sensory neurons
○ Role in mechanosensation
○ Pain and cough signal transmission
○ ATP release from tissue damage
○ Mechanical stress
○ Inflammatory mediators
○ Cellular distortion
○ Calcium influx
○ Membrane depolarization
○ Action potential generation
○ Afferent signal transmission
○ Upregulation of receptor expression
○ Enhanced ATP sensitivity
○ Reduced desensitization
○ Amplified response
○ Substance P
○ Neurokinin A
○ Neurokinin B
○ Calcitonin gene-related peptide (CGRP)
○ NK1 receptors
○ NK2 receptors
○ NK3 receptors
○ Distribution patterns
○ Neurogenic inflammation
○ Smooth muscle contraction
○ Vascular permeability
○ Sensory nerve activation
○ Enhanced release
○ Receptor upregulation
○ Altered neural processing
○ Chronic sensitization
○ Randomized, double-blind, placebo-controlled
○ 2:1 active drug to placebo ratio
○ Multiple study sites
○ Assessment of safety and efficacy
○ Chronic cough ≥ 1 year
○ Failed conventional treatments
○ Normal chest imaging
○ Specific cough frequency threshold >20 per hour
○ Uncontrolled comorbidities
○ Recent medication changes
○ Specific contraindications
○ Primary: Cough frequency reduction
○ Secondary: Quality of life measures
○ Safety assessments
○ Biomarker analysis
○ 2:1 randomization ratio
○ 66.7% chance of active drug
○ 33.3% chance of placebo
○ Double-blind maintenance
○ Regular site visits
○ Cough monitoring
○ Safety assessments
○ Compliance measures
○ Adverse event reporting
○ Regular safety assessments
○ Laboratory monitoring
○ Independent safety review
○ Trigger patterns
○ Associated symptoms
○ Treatment response
○ Impact on quality of life
○ Upper airway evaluation
○ Chest examination
○ Neurological assessment
○ Trigger point identification
○ Chest imaging
○ Pulmonary function tests
○ ENT examination
○ pH monitoring when indicated
○ Methacholine challenge
○ Induced sputum analysis
○ Allergy testing
○ Bronchoscopy when indicated
○ Gabapentin
○ Pregabalin
○ Amitriptyline
○ Low-dose morphine
○ Cough suppression techniques
○ Breathing exercises
○ Vocal hygiene
○ Behavioral modification
○ Mechanism of action
○ Expected benefits
○ Safety profile
○ Patient selection
○ Neurokinin antagonists
○ Combined approaches
○ Targeted therapies
○ Personalized medicine
○ Clinical features
○ Failed treatments
○ Risk assessment
○ Benefit potential
○ Objective measures
○ Patient-reported outcomes
○ Quality of life assessment
○ Safety parameters
○ Multiple modalities
○ Sequential approach
○ Risk-benefit assessment
○ Cost considerations
○ Duration of therapy
○ Monitoring requirements
○ Outcome assessment
○ Follow-up planning
○ Neural pathway characterization
○ Biomarker development
○ Phenotype identification
○ Treatment response prediction
○ Novel therapeutic targets
○ Combination approaches
○ Treatment algorithms
○ Cost-effectiveness studies