Pulmonary Adverse Effects of Streptokinase
When streptokinase is administered intravenously for systemic thrombolysis (e.g., pulmonary embolism), pulmonary hemorrhage is a rare but life-threatening complication that presents with massive hemoptysis, acute respiratory distress, and diffuse bilateral lung infiltrates; suspect this immediately in any patient developing sudden respiratory compromise after streptokinase administration. 1
Systemic (Intravenous) Administration for Pulmonary Embolism
Major Pulmonary Complications
Pulmonary hemorrhage is the most serious pulmonary-specific adverse effect, manifesting as:
Adult respiratory distress syndrome (ARDS) has been reported, though this occurred in a patient receiving both streptokinase and urokinase 2
Monitoring Strategy for Systemic Use
Monitor continuously for sudden respiratory compromise during and immediately after streptokinase infusion, as pulmonary hemorrhage can develop acutely 1
Obtain urgent chest imaging (chest X-ray or CT) if new dyspnea, hemoptysis, or oxygen desaturation occurs 1
Check serial hemoglobin levels to detect occult bleeding, particularly in patients with respiratory symptoms 1
Assess oxygenation status with pulse oximetry and arterial blood gases if respiratory distress develops 1
Management of Pulmonary Hemorrhage
Immediately discontinue streptokinase if pulmonary hemorrhage is suspected 1
Provide supportive care including oxygen supplementation, mechanical ventilation if needed, and blood transfusion for severe anemia 1
Conservative management with cessation of thrombolysis and supportive measures can lead to recovery in some patients 1
Recognize that mortality is significant when pulmonary hemorrhage occurs, with death from respiratory failure reported 1
Intrapleural (Local) Administration for Pleural Infections
Common Adverse Effects
Pleural pain (chest pain) occurs in approximately 7% of patients receiving intrapleural streptokinase versus 3% with placebo 2
Fever is commonly noted with streptokinase, though distinguishing drug-induced fever from infection-related fever can be challenging 3, 2
Immunological reactions occur most frequently with streptokinase due to its bacterial-derived antigenic properties 3, 2
Rare but Serious Complications
Local pleural hemorrhage has been reported, including one pediatric case of significant bleeding after traumatic drain insertion 3, 2
Systemic bleeding manifestations including epistaxis (nosebleeds) are rare 4, 2
Transient disorientation without evidence of intracerebral bleeding has been documented 4, 2
Critical Safety Considerations for Intrapleural Use
Streptokinase generates persistent neutralizing antibodies similar to systemic administration, even when given intrapleurally 3, 4
Re-administration within 6 months is contraindicated due to risk of severe allergic reactions and loss of efficacy 4
Provide patients with a streptokinase exposure card to document prior use 4, 2
For any subsequent thrombolytic indication (myocardial infarction, pulmonary embolism), use urokinase or tissue plasminogen activator instead of streptokinase 4, 2
No systemic fibrinolysis occurs at cumulative intrapleural doses up to 1.5 million IU, based on safety monitoring 4, 2
Common Pitfalls to Avoid
Do not dismiss new respiratory symptoms as anxiety or underlying disease progression—always consider pulmonary hemorrhage in patients receiving systemic streptokinase 1
Do not attribute all fever to the underlying infection when streptokinase is used intrapleurally; drug-induced fever is common 3, 2
Do not exceed cumulative intrapleural doses of 1.5 million IU to avoid potential systemic fibrinolytic effects 4
Do not use streptokinase for repeat thrombolysis within 6 months due to antibody formation 4
Avoid intrapleural fibrinolytics within 24 hours of traumatic chest tube insertion due to increased bleeding risk 3
Alternative Agents with Lower Pulmonary Risk
Urokinase is non-antigenic (derived from human urine) and carries lower immunological risk than streptokinase 3, 4, 2
For intrapleural use, urokinase 100,000 IU once daily for 3 days is equally effective to streptokinase with fewer immunological reactions 4, 2
For systemic pulmonary embolism, alteplase (rtPA) 100 mg over 2 hours provides similar efficacy to streptokinase with potentially lower antigenic risk 3, 5