How do you interpret and manage abnormal arterial blood gas (ABG) results?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: November 7, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

ABG Interpretation and Management

Systematic Approach to Interpretation

Interpret ABG results using a three-step systematic approach: first evaluate pH to determine acidemia or alkalemia, then examine PaCO2 to identify the respiratory component, and finally evaluate base excess/bicarbonate to identify the metabolic component. 1, 2

Step 1: Assess pH

  • pH < 7.35: Acidemia present 1
  • pH > 7.45: Alkalemia present 1
  • pH 7.35-7.45: May still represent compensated disorder or mixed disorder—do not stop here 3, 4

Step 2: Evaluate PaCO2 (Respiratory Component)

  • PaCO2 > 45 mmHg with low pH: Respiratory acidosis 5, 1
  • PaCO2 < 35 mmHg with high pH: Respiratory alkalosis 1
  • Critical caveat: A "normal" PaCO2 in the setting of hypoxemia indicates severe ventilatory failure—the patient should be hypocapnic if truly compensating 3

Step 3: Evaluate Base Excess/Bicarbonate (Metabolic Component)

  • Base excess < -2 or HCO3 < 22: Metabolic acidosis 6, 2
  • Base excess > +2 or HCO3 > 26: Metabolic alkalosis 6, 2
  • In primary respiratory disorders, base excess should remain normal initially; in chronic respiratory disorders, base excess changes to compensate 6

Step 4: Determine Compensation vs. Mixed Disorder

  • Acute disorders: Minimal compensation present 6, 2
  • Chronic disorders: Significant compensation with base excess changes 6
  • Mixed disorders: pH, PaCO2, and base excess all point in different directions 4, 7

Primary Indications for ABG Testing

Critical Situations Requiring Immediate ABG

  • All critically ill patients to assess oxygenation, ventilation, and acid-base status 1, 2
  • Patients with shock or hypotension—obtain arterial sample initially 1, 2
  • Oxygen saturation fall below 94% on room air or supplemental oxygen 1, 2
  • Deteriorating oxygen saturation (≥3% fall) or increasing breathlessness in patients with previously stable chronic hypoxemia 1, 2

Metabolic Indications

  • Suspected diabetic ketoacidosis 1, 2
  • Metabolic acidosis from renal failure 1, 2
  • Trauma, shock, and sepsis—base excess guides resuscitation effectiveness 6, 2
  • Suspected toxic ingestions 6

Monitoring Requirements

  • Within 60 minutes of starting oxygen therapy in COPD patients 1, 2
  • Within 60 minutes of any change in inspired oxygen concentration 1, 2
  • After each oxygen titration in patients with baseline hypercapnia 1, 2
  • Every 6 months in hepatopulmonary syndrome to monitor for worsening hypoxemia 5, 2

Management of Abnormal ABG Results

Respiratory Acidosis (High PaCO2, Low pH)

For acute hypercapnic respiratory failure with pH < 7.35 and PaCO2 > 6.5 kPa (49 mmHg) despite optimal medical therapy, initiate non-invasive ventilation (NIV). 5

Oxygen Therapy in At-Risk Patients

  • Start with controlled oxygen therapy targeting SpO2 88-92% in COPD and all causes of acute hypercapnic respiratory failure 5
  • Begin at 1 L/min via nasal cannula, titrate up in 1 L/min increments until SpO2 > 90% 1
  • Repeat ABG after each titration to monitor for worsening hypercapnia 1, 2
  • Patients who develop respiratory acidosis (PaCO2 rise > 1 kPa or 7.5 mmHg) during oxygen therapy require further medical optimization 1

NIV Initiation and Monitoring

  • Start NIV when pH < 7.35 and PaCO2 > 6.5 kPa persist despite optimal medical therapy 5
  • Severe acidosis alone does not preclude NIV trial if performed in appropriate setting with intubation capability 5
  • Obtain ABG prior to and following NIV initiation 5
  • Maximize NIV time in first 24 hours depending on tolerance 5
  • Worsening pH and respiratory rate indicate need to change strategy—adjust settings, change interface, or proceed to intubation 5

Discontinuation Criteria

  • Discontinue NIV when pH and PaCO2 normalize with general clinical improvement 5
  • Taper daytime NIV over 2-3 days depending on PaCO2 before discontinuing overnight 5

Metabolic Acidosis (Low HCO3/Base Excess, Low pH)

Treat the underlying cause first—bicarbonate therapy should be planned stepwise since response is not precisely predictable. 8

Bicarbonate Administration

  • Cardiac arrest: Initial rapid IV dose of 44.6-100 mEq (one to two 50 mL vials), continue 44.6-50 mEq every 5-10 minutes as indicated by arterial pH and blood gas monitoring 8
  • Less urgent metabolic acidosis: 2-5 mEq/kg body weight over 4-8 hours depending on severity 8
  • Monitor therapy by measuring blood gases, plasma osmolarity, arterial lactate, hemodynamics, and cardiac rhythm 8

Critical Management Principles

  • Do not attempt full correction of low total CO2 in first 24 hours—may cause unrecognized alkalosis due to delayed ventilatory readjustment 8
  • Target total CO2 of approximately 20 mEq/L at end of first day, which usually associates with normal blood pH 8
  • Values brought to normal or above normal within first day are very likely associated with grossly alkaline blood pH 8

Common Pitfalls to Avoid

Interpretation Errors

  • Normal oxygen saturation does not rule out significant acid-base disturbances or hypercapnia—pulse oximetry will be normal in patients with abnormal acid-base status or anemia 1, 2
  • Failing to recognize that normal PaCO2 with hypoxemia indicates severe ventilatory failure 3
  • Normal pH does not exclude acid-base disorders—must evaluate PaCO2 and bicarbonate 3, 4

Technical Errors

  • Air bubbles in sample alter results—ensure sample is free of air and rapidly processed 3
  • Must interpret results within clinical context—if absolutely incompatible with clinical situation, repeat probe 3
  • Body temperature and FiO2 are mandatory for adequate interpretation 3

Management Errors

  • Not repeating ABG after oxygen therapy changes, especially in CO2 retainers 1, 2
  • Failing to wait for steady state conditions after FiO2 changes, particularly in ventilation-perfusion mismatch (COPD, pneumonia, pulmonary embolism) 3
  • Overlooking need for ABG in metabolic conditions causing acid-base disturbances 1, 2
  • Delaying NIV initiation when indicated or conversely delaying intubation when NIV is inappropriate 5

Special Populations

  • COPD/fixed airflow obstruction: Check ABG when starting oxygen, especially with known CO2 retention 1, 2
  • Age ≥ 65 years: Use P(A-a)O2 ≥ 20 mmHg cutoff instead of ≥ 15 mmHg for hepatopulmonary syndrome diagnosis 5
  • Hepatopulmonary syndrome: PaO2 < 80 mmHg or P(A-a)O2 ≥ 15 mmHg (≥ 20 mmHg if age ≥ 65) warrants further investigation 5

References

Guideline

Arterial Blood Gas Analysis Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Arterial Blood Gas Analysis in Critical Care

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

[Fallacies in arterial blood gas interpretation].

Therapeutische Umschau. Revue therapeutique, 2013

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Base Excess in Critical Care

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Interpretation of arterial blood gas.

Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine, 2010

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.