Monday, November 20, 2017
Sunday, November 19, 2017
Saturday, November 18, 2017
Appropriate and inappropriate use of troponin assays
The article offers a
useful perspective on troponin testing but, if I’m not mistaken
(correct me if I’m wrong) starts out with an error:
Troponin is a protein in striated muscle that regulates excitation and contraction, and consists of 3 molecules: C, I, and T. Troponin I and T are specific to cardiac tissue…
I’m pretty sure
skeletal muscle has troponin I and T.
At any rate, the key
point of the article is that in the old days of the early generation
troponins, any elevation meant the patient was having an acute MI,
usually due to acute coronary syndrome. Several generations (and
sensitivity improvements) later that is no longer the case. The
problem is, too many of us apparently interpret troponins the way we
did in those good old days. This, as the author points out, can lead
to problems such as knee jerk anticoagulation.
The remedy for this,
according to the author, is to do a history and physical before
ordering a troponin. That’s easier said than done in the crazy
environment of hospital medicine where time is of the essence and we
often have to utilize a shotgun approach to very sick patients. The
reality is that troponin positivity has now become much more complex
and requires considerable skill in applying the result to the
prevailing clinical context.
Friday, November 17, 2017
Thursday, November 16, 2017
Your critically ill patient went into atrial fibrillation. Amiodarone was started. Now what?
Sound familiar?
This paper makes the case for cardiology consultation, at
least if the drug is going to be continued at discharge.
Wednesday, November 15, 2017
Tuesday, November 14, 2017
Monday, November 13, 2017
Sunday, November 12, 2017
Fluid overload and sepsis and using bioimpedence to monitor it
Guideline-directed therapy for sepsis calls for early fluid resuscitation. Often patients receive large volumes of intravenous fluids. Bioimpedance vector analysis (BIVA) is a noninvasive technique useful for measuring total body water. In this prospective observational study, we enrolled 18 patients admitted to the intensive care unit for the treatment of sepsis syndromes. Laboratory data, clinical parameters, and BIVA were recorded daily. All but one patient experienced volume overload during the course of treatment. Two patients had greater than 20 L of excess volume. Volume overload is clinically represented by tissue edema. Edema is not a benign condition, as it impairs tissue oxygenation, obstructs capillary blood flow, disrupts metabolite clearance, and alters cell-to-cell interactions. Specifically, volume overload has been shown to impair pulmonary, cardiac, and renal function. A positive fluid balance is a predictor of hospital mortality. As septic patients recover, volume excess should be aggressively treated with the use of targeted diuretics and renal replacement therapies if necessary.
Saturday, November 11, 2017
EP testing in bradyarrhythmias
This free full text
review deals mainly with the various mechanisms of AV block,
clues on the surface ECG and when EP testing is needed.
Friday, November 10, 2017
Arrhythmogenic cardiomyopathy (aka arrhythmogenic right ventricular cardiomyopathy/dysplasia)
The new terminology
relates to the increasing recognition of left ventricular
involvement. Free full text review.
Thursday, November 09, 2017
Wednesday, November 08, 2017
Tuesday, November 07, 2017
Monday, November 06, 2017
Liberal versus restrictive transfusion strategy: the debate is not quite over
Although a
hemoglobin of 7 has become a widely accepted threshold for
transfusion in a variety of situations there remain areas of
uncertainty. One of these areas is ischemic heart disease. The NIH
sponsored MINT is being organized to address this question.
(Public Citizen thinks it should not be carried out). One of
the questions here is whether there is equipoise for such a trial.
Public Citizen, while leveling their principal objections toward
trial ethics and the informed consent process, implies that there is
no equipoise and a higher hemoglobin threshold should be accepted.
The argument that equipoise exists is based on the fact that for
ischemic heart disease there are only low level data to guide
transfusion practices. High level trials lumped patients together
having many different underlying diseases. How might transfusion
thresholds apply to various subgroups? That raises nearly endless
questions.
What about, for
example, oncology patients with septic shock? Check out the results of this single center RCT:
Objective: To assess whether a restrictive strategy of RBC transfusion reduces 28-day mortality when compared with a liberal strategy in cancer patients with septic shock.
Design: Single center, randomized, double-blind controlled trial.
Setting: Teaching hospital.
Patients: Adult cancer patients with septic shock in the first 6 hours of ICU admission.
Interventions: Patients were randomized to the liberal (hemoglobin threshold, less than 9 g/dL) or to the restrictive strategy (hemoglobin threshold, less than 7 g/dL) of RBC transfusion during ICU stay.
Measurements and Main Results: Patients were randomized to the liberal (n = 149) or to the restrictive transfusion strategy (n = 151) group. Patients in the liberal group received more RBC units than patients in the restrictive group (1 [0–3] vs 0 [0–2] unit; p less than 0.001). At 28 days after randomization, mortality rate in the liberal group (primary endpoint of the study) was 45% (67 patients) versus 56% (84 patients) in the restrictive group (hazard ratio, 0.74; 95% CI, 0.53–1.04; p = 0.08) with no differences in ICU and hospital length of stay. At 90 days after randomization, mortality rate in the liberal group was lower (59% vs 70%) than in the restrictive group (hazard ratio, 0.72; 95% CI, 0.53–0.97; p = 0.03).
Conclusions: We observed a survival trend favoring a liberal transfusion strategy in patients with septic shock when compared with the restrictive strategy. These results went in the opposite direction of the a priori hypothesis and of other trials in the field and need to be confirmed.
This contributes to
the evidence we have to guide transfusion practices but also serves
as a reminder that there is no pat answer. Clinical judgment must
surpass slavish adherence to pathways and guidelines, which is what
evidence based medicine is all about.
Sunday, November 05, 2017
Saturday, November 04, 2017
Friday, November 03, 2017
Thursday, November 02, 2017
Assessment of fluid responsiveness is associated with improvement in robust outcomes
The big question is
how invasive you need to be to accomplish this.
Wednesday, November 01, 2017
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