Shock Syndromes II
Impaired systolic function (massive PE): Embolism dissolution (thrombolytic therapy) or removal
(surgical or catheter thrombectomy)
Thrombolytic agents (Table 9) bind to the plasminogen/plasmin complex, which may be either
circulating or bound to the clot surface.
ii.
This binding hydrolyzes a peptide bond to form free plasmin. Circulating plasmin is quickly
neutralized by Ξ±-antiplasmin, but fibrin-bound plasmin subsequently hydrolyzes bonds within
the clot matrix, leading to clot lysis.
iii.
As such, thrombolytic agents can lead to rapid PE dissolution and a subsequent decrease in RV
afterload (pulmonary vascular resistance), but they may also cause bleeding.
Drug
Dose
Pearl
Initial
Infusion
Alteplasea
Total dose: 100 mg infused over 2 hr
Fibrin selective half-life: 5 min
Dose in cardiac arrest may be
50 mg
Reteplaseb
Two doses of 10 units IV push over 2 min,
given 30 min apart
Fibrin selective half-life: 13β16
min
Tenecteplaseb
< 60 kg: 30-mg push over
5β10 s
61β70 kg: 35-mg push
71β80 kg: 40-mg push
81β90 kg: 45-mg push
> 91 kg: 50-mg push
N/A
Fibrin selective (14-fold com-
pared with alteplase) half-life:
90β130 min; only need bolus
dose
Less expensive than alteplase
Streptokinaseb
250,000 units over 30 min
100,000 units/hr over 24 hr
Nonselective
Antigenic
Urokinasea
4400 units/kg over 10 min
4400 units/kg/hr over 12 hr
Nonselective
aIndicates FDA approved for the treatment of PE.
bIndicates drug is not FDA approved for the treatment of PE.
PE = pulmonary embolism.
2012;32:158-72.
iv.
In a 2004 meta-analysis, thrombolytic agents were not shown to decrease mortality when
evaluated among all patients with a PE compared with heparin alone (6.7% vs. 9.6%; OR 0.67
[95% CI, 0.40β1.12]), but they may improve outcomes in patients with an increased risk of
death. As such, early PE-related mortality risk stratification is necessary to guide thrombolytic
therapy administration.
| (a) | High-risk or massive PE. Defined by the 2011 American Heart Association (AHA) |
|---|
guidelines not by clot burden, but by acute PE causing hemodynamic changes: Hypotension
(SBP less than 90 mm Hg for at least 15 minutes or requiring vasoactive support not
from another cause), pulselessness, or bradycardia (heart rate less than 40 beats/minute
with signs of shock). The 2019 European Society of Cardiology (ESC) and European
Respiratory Society (ERS) guidelines for acute PE define hemodynamic instability as
including one of the following presentations:
| (1) | Cardiac arrest, |
|---|---|
| (2) | Obstructive shock (SBP less than 90 mm Hg or vasopressors required to achieve SBP |
of 90 mm Hg or greater despite adequate filling status AND end-organ hypoperfusion),
or