Cardiovascular Critical Care I
Dobutamine and milrinone are most often used for suspected or confirmed low cardiac output
states. Milrinone may be preferred more than dobutamine in the presence of recent administration
of β-blockade or in the setting of concomitant pulmonary hypertension (because of its post-β
receptor effects and potent vasodilatory properties, respectively). In terms of pharmacokinetic
differences, dobutamine has a faster onset and shorter half-life (2 min) compared with milrinone
(half-life of 3 hrs with renal-dependent elimination). However, no differences in clinical efficacy
or safety have been observed between agents. Both agents should be closely monitored for the
development of proarrhythmias and worsening ischemia.
Evaluate for the appropriate initiation of GDMT
Current guidelines recommend initiation of a 4-drug regimen for most patients with HFrEF as soon
as possible, including in the inpatient setting. This 4-drug regimen is a combination of a RAAS
inhibitor (angiotensin receptor/neprilysin inhibitor preferred), beta blocker, MRA, and sodium
glucose co-transporter 2 inhibitor. For further guidance on GDMT indications, please consult
current HF guidelines (Circulation 2022;145:e895-1032).
Many providers discontinue β-blockers in acute decompensated HF, but this practice is generally
not recommended because research indicates it can significantly increase the risk of in-hospital and
short-term mortality, given the potential for increased sympathetic nervous system activation upon
abrupt discontinuation. β-Blockers should be continued in patients with acute decompensated HF
unless there are specific clinical reasons to discontinue them, like severe hemodynamic instability
or evidence of shock (Eur Heart J. 2009;30(18):2186-2192).
management of the critically ill patient. Valvular heart disease can also independently lead to the presenting
critical illness.
depth and breadth of these etiologies are beyond the scope of this chapter. Nevertheless, conditions that may
require repair/replacement include those listed in Table 12.
Stenosis
Narrowing at the opening of the valve(s)
Can lead to concurrent regurgitation
Regurgitation
“Leaky” valve(s) resulting in less blood pumping forward through the heart
Prolapse
“Floppy” valve(s) with part of valve not working
Endocarditis
Infection of one or more valves
Malformation
Often occurs at birth when the valve (or valves) is defective
aValvular disease secondary to rheumatic heart disease is a rare but possible contributor.