Index
Module 12 • Cardiology
Cardiovascular Critical Care II
31%
Data Tables
Cardiovascular Critical Care II
Patrick M. Wieruszewski ~3 min read Module 12 of 20
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Cardiovascular Critical Care II

Medication background (rhythm independent considerations)

Goal: Increase myocardial blood flow during CPR and help achieve ROSC

ii.

Drug delivery

(a)Central intravenous administration is recommended, if available. Central line placement

should not interrupt CPR. The advantage of central administration is higher peak

concentration and shorter drug circulation times than with peripheral routes (Crit Care
Med 1988;16:1138-41; Ann Emerg Med 1981;10:73-8; Ann Emerg Med 1981;10:417-9).
(b)If peripheral administration of medications is necessitated, a bolus injection should be

followed by a 20-mL bolus of an intravenous fluid (e.g., 0.9% sodium chloride) to facilitate

drug flow from the extremity to the central circulation (Am J Emerg Med 1990;8:190-3).
(c)If proximal humerus intraosseous (IO) access is used, administration and drug delivery

are similar to central venous access. If proximal or distal tibial intraosseous access is

used, administration and drug delivery are similar to peripheral venous access and would

necessitate a 20-mL bolus or pressure bag to facilitate drug administration. In a randomized

cadaver study, tibial IO access has been shown to be easier to obtain, which allows for

faster medication administration (Medicine 2016; 95: e3724). Data analyses suggest that

intraosseous access is associated with poorer OHCA survival and fewer favorable neurologic

outcomes, even after controlling for many other variables (Ann Emerg Med 2018;71:588-

96). Intraosseous access may have initially been selected by first responders because of

perceived complexity and influential patient characteristics. However, additional analysis

has found that tibial intraosseous access compared with intravenous access is associated

with a lower likelihood of ROSC and survival to hospitalization (Resuscitation 2017;117:91-

6). The most recent guidelines now support the use of intravenous access preferentially

unless it cannot be obtained (Circulation 2020;142:S366-S468). In these circumstances,

intraosseous access is reasonable.

(d)Endotracheal (ET) delivery
(1)NAVEL acronym summarizes medications that have been studied and shown to have

tracheal absorption by ET tube delivery. N – naloxone, A – atropine, V – vasopressin,

E – epinephrine, L – lidocaine.

(2)Serum concentrations of medications are lower when given by ET delivery.
(3)Optimal ET doses unknown; typically, they are 2–2.5 times intravenous doses but may
be higher (e.g., up to 3–10 times higher for epinephrine) (Crit Care Med 1987;15:1037-9).
(4)Should be diluted with either 5–10 mL of 0.9% sodium chloride or sterile water and

injected directly into the ET tube, ideally during pulse check to avoid medication

expulsion back out the ET (Crit Care Med 1994;22:1174-80)
(e)Peak effect of intravenous or intraosseous medication delayed 1–2 minutes during CPR.
(f)Theoretical concern that giving high-dose bolus vasopressors after ROSC following

defibrillation may precipitate cardiac instability and re-arrest. May be avoided by using

physiological monitoring such as quantitative waveform capnography, intra-arterial

pressure monitoring, or continuous central venous oxygen saturation monitoring and

avoiding administration of vasopressors if ROSC occurs (J Emerg Med 2009;38:614-21;

Ann Emerg Med 1992;21:1094-101; Ann Emerg Med 1990;19:1104-6).
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