GlobalRPh Pulmonary Medicine, Respiratory Pharmacotherapy and Gas Exchange Resources

Pulmonary Medicine Clinical Resource Center

Clinician-focused resources for asthma, COPD, gas exchange and arterial blood gases, pulmonary function testing, pulmonary embolism, pulmonary hypertension, interstitial lung disease and IPF, sleep-disordered breathing, respiratory infection, lung cancer screening, inhaled pharmacotherapy, laboratory support, and current GlobalRPh pulmonary reviews.

Primary audience: physicians, pharmacists, nurses, respiratory therapists, advanced practice clinicians, and other healthcare professionals involved in respiratory diagnosis, pharmacotherapy, monitoring, and acute or chronic pulmonary care.

Clinical framework

Respiratory symptoms require physiologic, structural, and disease-specific interpretation

Dyspnea, cough, wheeze, hypoxemia, hypercapnia, exercise intolerance, and abnormal imaging can result from airway disease, parenchymal disease, pulmonary vascular disease, infection, cardiac disease, neuromuscular dysfunction, obesity, anemia, deconditioning, medication effects, or combinations of these processes. Pulmonary assessment therefore requires integration of history, physical findings, oxygenation, ventilation, pulmonary function, imaging, laboratory data, and response to therapy.

We reorganize our Pulmonary resources by clinical problem rather than by isolated drug class. The portal retains our established respiratory medication tables and gas-exchange calculators while adding current guideline pathways, pulmonary vascular resources, interstitial lung disease, sleep medicine, pulmonary embolism, and lung cancer screening.

Ventilation Assess respiratory drive, mechanics, dead space, PaCO2, and the adequacy of alveolar ventilation.
Oxygenation Interpret PaO2, SaO2, FiO2, hemoglobin, A-a gradient, shunt, and V/Q relationships in context.
Airflow Use objective spirometry and clinical history to distinguish variable from persistent airflow limitation.
Structure / vasculature Integrate imaging, diffusion capacity, hemodynamics, thromboembolic disease, and interstitial abnormalities.
1. Define the syndrome Acute versus chronic, obstructive versus restrictive, hypoxemic versus hypercapnic, focal versus diffuse.
2. Confirm objective physiology Use pulse oximetry, ABG, spirometry, lung volumes, DLCO, exercise testing, or hemodynamics as appropriate.
3. Match treatment to phenotype Use disease-specific guidance rather than applying a generic inhaler or oxygen strategy.
4. Reassess response and risk Track exacerbations, symptoms, oxygenation, lung function, adverse effects, adherence, and inhaler technique.
Pulmonary Medicine Clinical Illustration

Pulmonary calculators and clinical decision support

Gas exchange, oxygen content, pulmonary embolism, and critical-care crossover tools

The legacy Pulmonary page exposed only two calculators. We retain those tools and add relevant GlobalRPh pulmonary embolism and critical-care calculations while distinguishing older disease pages from current clinical decision support.

Legacy COPD calculator: the GlobalRPh COPD calculator page currently states that it was being revised and that an updated version was expected in January 2019. We are not presenting that page as an active COPD decision-support tool. COPD diagnosis and treatment should be aligned with current GOLD guidance.

Gas exchange, oxygenation, ventilation, and acid-base assessment

ABG interpretation requires physiologic context rather than isolated threshold values

Arterial blood gases can define oxygenation, ventilation, and acid-base status, but results must be interpreted with FiO2, altitude/barometric pressure, hemoglobin, temperature when relevant, ventilatory support, clinical trajectory, and the mechanism of respiratory failure.

A-a gradient

The A-a gradient can help differentiate hypoventilation or low inspired oxygen from abnormalities involving V/Q mismatch, diffusion limitation, or shunt. Interpretation depends on age, FiO2, barometric pressure, and the assumptions used in the alveolar gas equation.

Arterial oxygen content

Oxygen content incorporates hemoglobin concentration and oxygen saturation in addition to dissolved PaO2. A satisfactory PaO2 does not guarantee adequate arterial oxygen content when hemoglobin concentration is substantially reduced.

Our older pulmonary physiology and ABG pages contain historical teaching thresholds, compensation rules, terminology, and ventilatory-support statements that should be reviewed against contemporary pulmonary and critical-care practice. We retain these pages for educational continuity while prioritizing formal modernization.

Pulmonary function testing

Spirometry, lung volumes, diffusion capacity, and physiologic pattern recognition

Pulmonary function tests classify physiologic impairment and support diagnosis when integrated with clinical findings. Contemporary ATS/ERS interpretation emphasizes appropriate reference equations, lower limits of normal and z-scores, quality criteria, and careful distinction between obstructive, restrictive, mixed, and diffusion abnormalities.

Interpretive framework

  • Verify acceptability and repeatability before interpretation
  • Use appropriate reference equations and lower limits of normal
  • Confirm restriction with lung-volume measurement when indicated
  • Interpret DLCO with hemoglobin and relevant clinical variables
  • Use PFT patterns to classify physiology, not as a stand-alone disease diagnosis

GlobalRPh modernization opportunity

The current Pulmonary portal has no dedicated PFT section. We plan to develop a structured PFT interpretation resource using contemporary ATS/ERS standards, z-score based interpretation, bronchodilator response, lung volumes, and diffusion capacity.

Asthma

Diagnosis, anti-inflammatory treatment, exacerbation prevention, and severe-asthma phenotype assessment

Asthma management requires confirmation of variable expiratory airflow limitation when possible, assessment of symptom control and exacerbation risk, inhaler technique, adherence, comorbidities, environmental exposures, and selection of anti-inflammatory therapy appropriate to the patient.

Several GlobalRPh asthma medication tables include discontinued products, older devices, older approval language, and historical controller strategies. We retain them for drug-reference continuity while we reconcile current marketed products, current labeling, GINA 2026 treatment positioning, biologic options, device selection, and inhaler-technique guidance.

Chronic obstructive pulmonary disease

Objective airflow obstruction, symptom burden, exacerbation risk, inhaled therapy, and comorbidity management

COPD diagnosis requires appropriate clinical context and objective confirmation of persistent airflow obstruction. Management extends beyond bronchodilator selection to smoking cessation, vaccination, pulmonary rehabilitation, exacerbation prevention, oxygen assessment, inhaler technique, comorbidity management, and individualized follow-up.

Historical GlobalRPh COPD calculator

This page states that a revision was expected in January 2019 and should not be interpreted as a current COPD staging or treatment algorithm.

The 2025 GlobalRPh review on asthma-COPD overlap is retained as a diagnostic discussion, but current therapy should be anchored to the patients confirmed disease characteristics and current GINA/GOLD guidance rather than to an undifferentiated overlap label.

Pulmonary embolism and venous thromboembolism

Pretest probability, diagnostic testing, acute risk classification, anticoagulation, and follow-up

In 2026, a multisociety AHA/ACC guideline introduced a new acute PE clinical classification framework and comprehensive recommendations spanning diagnosis, treatment, disposition, and post-PE follow-up. We place this current guidance beside our longstanding Wells and thrombolytic resources.

Modernization priority

Our Wells PE calculator cites older diagnostic reviews. The score itself remains established, but we plan to place it within a current diagnostic pathway incorporating validated pretest probability, D-dimer strategy, imaging selection, the 2026 acute PE categories, and post-PE assessment.

Pulmonary hypertension

Classification, hemodynamic confirmation, risk assessment, and disease-specific therapy

Pulmonary hypertension is not a single disease and should not be treated as one. Classification, underlying mechanism, echocardiographic probability, right-heart catheterization when indicated, comorbid lung or left-heart disease, chronic thromboembolic disease, and referral to an experienced pulmonary hypertension center are central to appropriate management.

Key clinical distinctions

  • Pulmonary arterial hypertension
  • PH due to left-heart disease
  • PH due to lung disease / hypoxia
  • Chronic thromboembolic pulmonary hypertension
  • PH with unclear or multifactorial mechanisms
Our pulmonary hypertension drug table should not be used as a stand-alone treatment algorithm. PAH-specific therapies can be inappropriate or harmful in other forms of pulmonary hypertension. We plan to reorganize the table by current disease classification, risk pathway, drug class, combination strategy, and monitoring.

Interstitial lung disease and pulmonary fibrosis

IPF, progressive pulmonary fibrosis, connective-tissue-disease ILD, and multidisciplinary diagnosis

Interstitial lung disease requires integration of exposure history, autoimmune features, high-resolution CT pattern, pulmonary function, serology when indicated, and multidisciplinary discussion. Idiopathic pulmonary fibrosis and progressive pulmonary fibrosis have disease-specific diagnostic and therapeutic pathways.

Modernization priority

Our current IPF table is centered on pirfenidone and nintedanib-era monographs and should be updated for current labeling, progressive pulmonary fibrosis, monitoring, adverse-effect management, transplant referral, oxygen, rehabilitation, and multidisciplinary diagnostic standards.

Sleep-disordered breathing

Obstructive sleep apnea, cardiometabolic risk, PAP therapy, and perioperative implications

Obstructive sleep apnea is relevant to pulmonary medicine, cardiovascular risk, perioperative safety, resistant hypertension, obesity, arrhythmia, and daytime neurocognitive function. Screening instruments can identify risk but do not replace objective sleep testing when a diagnosis is required.

Clinical interpretation

  • Distinguish screening risk from diagnostic confirmation
  • Assess symptom burden and hypoxemic burden in context
  • Address PAP adherence and interface tolerance
  • Consider obesity, cardiometabolic disease, and sedating medications
  • Coordinate perioperative planning when clinically relevant

Respiratory infection

Pneumonia, RSV, influenza, tuberculosis, post-viral lung disease, and antimicrobial support

Pulmonary infection intersects with Infectious Disease, Critical Care, Pediatrics, and antimicrobial stewardship. We centralize pulmonary cross-links without duplicating antimicrobial treatment tables that are maintained in the Infectious Disease section.

Lung cancer screening and pulmonary oncology crossover

Risk-based low-dose CT screening, pulmonary nodules, and multidisciplinary referral

Lung cancer screening can reduce lung-cancer mortality in appropriately selected high-risk adults, but implementation requires eligibility assessment, shared decision-making, smoking-cessation support, standardized imaging pathways, and management of incidental or indeterminate findings.

Current USPSTF screening recommendation

The current USPSTF recommendation is annual low-dose CT for adults aged 50 to 80 years with a 20 pack-year smoking history who currently smoke or quit within the past 15 years, with defined criteria for discontinuation.

Clinical considerations

  • Smoking exposure and eligibility verification
  • Ability and willingness to pursue diagnostic evaluation and treatment
  • Shared decision-making and smoking cessation
  • Nodule follow-up and multidisciplinary pathways
  • Comorbidity, frailty, and competing mortality risk

Respiratory pharmacotherapy

GlobalRPh inhaled, systemic, biologic, pulmonary vascular, and antifibrotic drug references

We retain the medication categories from the existing Pulmonary portal but reorganize them by clinical role. Many individual tables were developed over multiple years and require ongoing reconciliation with current marketed products, device availability, FDA labeling, and disease-specific guidance.

Medication-table review status

Some GlobalRPh pulmonary tables still contain discontinued products, historical brand/device information, older warnings, and older guideline-era positioning. We preserve the references while updating product status, labeling, monitoring, and current therapeutic roles.

Alphabetical GlobalRPh drug index

GlobalRPh Pulmonology article library

Current and established pulmonary reviews

The legacy Pulmonary portal did not surface a functional article library. We now include current and established GlobalRPh reviews relevant to respiratory diagnosis, chronic airway disease, pulmonary vascular disease, sleep apnea, post-viral lung disease, infection, and lung cancer screening.

2026

GlobalRPh pulmonary video development

Respiratory topics for structured clinician education

The current GlobalRPh master video library does not contain a dedicated Pulmonary category. We retain respiratory videos located in Pediatrics or other sections and identify priority topics for a dedicated pulmonary video library.

Priority pulmonary video topics

  • GINA 2026 asthma treatment framework
  • GOLD 2026 COPD diagnosis and pharmacotherapy
  • ABG and A-a gradient interpretation
  • PFT interpretation using ATS/ERS standards
  • 2026 acute pulmonary embolism guideline
  • Pulmonary hypertension classification and referral
  • IPF and progressive pulmonary fibrosis
  • Inhaler device selection and technique
  • OSA screening versus diagnostic testing
  • Lung cancer screening eligibility and follow-up

Clinical content modernization

Priority updates within the GlobalRPh Pulmonary library

The Pulmonary section contains useful drug tables and physiologic calculators, but many pages were developed under older product, device, guideline, and disease-classification frameworks. We plan to preserve useful clinical content while modernizing product status, disease pathways, references, and decision-support language.

Priority resource reviews

  • COPD Calculator: retire or fully rebuild the incomplete page that still states an update was expected in January 2019. A replacement should incorporate current GOLD diagnosis, symptom/exacerbation assessment, eosinophil-informed ICS considerations, smoking cessation, vaccination, rehabilitation, oxygen, and follow-up.
  • Asthma Clinical Tool: develop a dedicated GlobalRPh asthma decision-support page anchored to GINA 2026, including confirmation of variable airflow limitation, symptom and exacerbation assessment, ICS-containing therapy, MART/SMART concepts where appropriate, inhaler technique, adherence, biologic phenotype, and referral criteria.
  • Inhaled Corticosteroids: update marketed products, age indications, device formulations, dose comparisons, local/systemic adverse effects, oral-rinse counseling, adrenal effects, and current GINA positioning.
  • Beta2 Agonists: remove obsolete products and historical oral beta-agonist emphasis, update SABA/LABA formulations, device information, rescue-versus-maintenance roles, cardiovascular effects, hypokalemia risk, and current asthma/COPD positioning.
  • Inhaled Anticholinergics: verify current marketed LAMA/SAMA products, COPD versus asthma indications, renal considerations, glaucoma/urinary-retention precautions, device technique, and combination-product availability.
  • Combination Inhalers: rebuild the table around current ICS/LABA, LAMA/LABA, and ICS/LABA/LAMA products, approved indications, device-specific dosing, asthma-versus-COPD roles, and current labeling.
  • Severe Asthma Biologics: expand beyond the existing IL-5 table to a phenotype-oriented biologic section including eosinophilic, allergic, and other supported pathways with current eligibility and monitoring considerations.
  • Mast Cell Stabilizers: distinguish historical respiratory products from currently available therapies and remove obsolete product/device references.
  • Theophylline / Aminophylline: clarify the limited contemporary role, therapeutic drug monitoring, narrow therapeutic index, interaction burden, age and disease effects on clearance, toxicity management, and current asthma/COPD positioning.
  • A-a Gradient Calculator: preserve the alveolar gas equation while updating assumptions, FiO2 limitations, age-adjusted interpretation, altitude/barometric-pressure considerations, and the distinction between A-a gradient and other oxygenation indices.
  • ABG Analysis: modernize terminology, compensation rules, mixed-disorder assessment, oxygenation interpretation, lactate/anion-gap crossover, and remove historical threshold statements that could be interpreted as protocol-level ventilator criteria.
  • Pulmonary Function Testing: build a new structured PFT interpretation resource based on contemporary ATS/ERS standards, z-scores, LLN, bronchodilator response, lung volumes, DLCO, quality assessment, and physiologic pattern recognition.
  • Pulmonary Embolism: integrate the Wells score into a current 2026 diagnostic and treatment pathway, including pretest probability, D-dimer strategy, imaging, acute PE clinical categories, anticoagulation, disposition, advanced therapy, and post-PE follow-up.
  • Pulmonary Hypertension: reorganize the drug table by current PH classification, hemodynamics, referral, PAH risk assessment, combination therapy, CTEPH, monitoring, and disease-specific contraindications.
  • IPF / Progressive Pulmonary Fibrosis: update the existing antifibrotic table with current ATS/ERS/JRS/ALAT guidance, progressive pulmonary fibrosis, monitoring, adverse-effect management, rehabilitation, oxygen, transplantation, and multidisciplinary diagnosis.
  • Sleep-Disordered Breathing: develop a dedicated clinician page covering screening, diagnostic testing, PAP therapy, adherence, cardiometabolic comorbidity, perioperative implications, and referral pathways.
  • Lung Cancer Screening: add a structured eligibility and follow-up resource incorporating current USPSTF criteria, shared decision-making, smoking cessation, LDCT implementation, nodule pathways, and oncology/thoracic-surgery referral.
Asthma 2026 clinical tool GINA-aligned confirmation, treatment tracks, exacerbation risk, biologic phenotype, and follow-up.
COPD 2026 decision support GOLD-aligned diagnosis, treatment grouping, eosinophils, exacerbations, rehabilitation, and oxygen assessment.
PFT interpretation tool ATS/ERS z-score and LLN framework with spirometry, lung volumes, DLCO, and pattern classification.
ABG / gas exchange 2.0 Integrated pH, PaCO2, bicarbonate, compensation, A-a gradient, oxygen content, and mixed-disorder analysis.
Acute PE 2026 pathway Pretest probability through diagnosis, risk category, treatment, disposition, and follow-up.
Inhaler comparison platform Current devices, drug classes, indications, technique, dose frequency, and disease-specific role.

Current external clinical standards

Authoritative respiratory guidance integrated with GlobalRPh pulmonary resources

Respiratory guidelines and technical standards evolve faster than many historical drug tables. We therefore provide direct access to current professional guidance while progressively updating our individual Pulmonary resources.

GINA 2026 Asthma Strategy Report Current global strategy for asthma diagnosis, control assessment, pharmacotherapy, exacerbation prevention, and severe asthma. Open GINA 2026
GOLD 2026 COPD Report and Pocket Guide Current evidence-based strategy for COPD diagnosis, assessment, prevention, maintenance therapy, exacerbations, and comorbidity. Open GOLD 2026
2026 AHA/ACC Multisociety Acute Pulmonary Embolism Guideline Current comprehensive guideline for adult acute PE evaluation, clinical categories, treatment, disposition, and follow-up. Open Acute PE Guideline
ERS/ATS Pulmonary Function Test Interpretation Technical standards for interpretation of routine lung function testing, including reference limits and physiologic pattern classification. Open PFT Interpretation Tools
2022 ESC/ERS Pulmonary Hypertension Guideline Comprehensive guideline for PH classification, diagnosis, hemodynamic assessment, PAH therapy, CTEPH, and disease-specific management. Open PH Guideline
2022 ATS/ERS/JRS/ALAT IPF and Progressive Pulmonary Fibrosis Current formal guideline update for idiopathic pulmonary fibrosis and progressive pulmonary fibrosis in adults. Open ILD / IPF Guideline
USPSTF Lung Cancer Screening Current federal preventive recommendation for annual low-dose CT screening in eligible high-risk adults. Open Lung Cancer Screening Recommendation
ATS Clinical Practice Guidelines, Statements, and Technical Standards Central professional index for oxygen therapy, pulmonary function, ILD, infection, pleural disease, and other pulmonary clinical standards. Open ATS Guideline Index

Supporting GlobalRPh clinical resources

Critical care, infectious disease, cardiology, oncology, pharmacokinetics, laboratory, and renal support

High-acuity and infection crossover

Cardiovascular / renal / PK support

Rationale for retaining established pulmonary medication and physiology pages

Many GlobalRPh respiratory drug tables and gas-exchange pages remain useful as references and are linked throughout longstanding clinical workflows. We are retaining those resources while modernizing product status, device information, FDA labeling, guideline positioning, diagnostic frameworks, and clinical warnings so historical content does not appear equivalent to current guidance.

Alphabetical Listing of individual drugs

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