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Update on the right to refuse antipsychotic medication.

The legal history and current developments in the right to refuse antipsychotic medication are reviewed. In Washington v. Harper the US Supreme Court analyzed the right to refuse antipsychotic medication under the due process clause of the Fourteenth Amendment to the US Constitution. A narrow issue was clarified but substantial uncertainty remains. As a result, law and policy problems at both state and institutional levels have become evident and may need to be addressed by drug policy decision makers.

Antipsychotic Agents↗

Heparin dosing and monitoring for cardiopulmonary bypass. A comparison of techniques with measurement of subclinical plasma coagulation.

Subclinical plasma coagulation during cardiopulmonary bypass has been associated with marked platelet and clotting factor consumption in monkeys. To better define subclinical coagulation in man, we measured plasma fibrinopeptide A concentrations before, during, and after cardiopulmonary bypass. Patients were assigned to one of three groups of heparin management: group 1 (n = 10)--initial heparin dose 300 IU/kg, with supplemental heparin if the activated coagulation time fell below 400 seconds; group 2 (n = 6)--initial heparin dose 250 IU/kg, with supplemental heparin if activated coagulation time was less than 400 seconds; and group 3 (n = 5)--initial heparin dose 350 to 400 IU/kg, with supplemental heparin if whole blood heparin concentration was less than or equal to 4.1 IU/ml. Activated coagulation time and heparin concentration were measured every 30 minutes during cardiopulmonary bypass, and fibrinopeptide A was measured at hypothermia, normothermia, and whenever activated coagulation time was less than 400 seconds. Quantitative and qualitative blood clotting competence was assessed after cardiopulmonary bypass, including mediastinal drainage for the first 24 hours. Fibrinopeptide A values were markedly elevated during cardiopulmonary bypass but were well below the levels present before and after cardiopulmonary bypass. Fibrinopeptide A correlated inversely with heparin concentration during cardiopulmonary bypass (r = -0.46, p = 0.03), but higher fibrinopeptide A levels during cardiopulmonary bypass did not correlate with post-cardiopulmonary bypass coagulopathy. Group 3 patients received the highest heparin doses (p less than 0.05) and had the greatest postoperative blood loss (p less than 0.05). Protamine dose and heparin concentration during cardiopulmonary bypass correlated best with postoperative mediastinal drainage. Our findings support the following conclusions: (1) compensated subclinical plasma coagulation activity occurs during cardiopulmonary bypass despite activated coagulation time greater than 400 seconds or heparin concentration greater than or equal to 4.1 IU/ml; (2) post-cardiopulmonary bypass mediastinal drainage correlates strongly with increased heparin concentration during cardiopulmonary bypass (p less than 0.05) and protamine dose (p less than 0.05); and (3) during cardiopulmonary bypass at both normothermia and hypothermia, activated coagulation times greater than 350 seconds result in acceptable fibrinopeptide A levels and post-cardiopulmonary bypass blood clotting.

Blood Coagulation↗

Impact of atropine injection on heart rate response during treadmill exercise echocardiography: a double-blind randomized pilot study.

We evaluated the effect of atropine on the heart rate (HR) response during treadmill exercise echocardiography. A potential limitation of treadmill exercise echocardiography is the requirement for postexercise imaging. Rapid recovery of HR and wall motion abnormalities may decrease test sensitivity. A double-blind randomized study was performed at a tertiary care center. Fifty-two patients (age, 63 +/- 9 years) with known or suspected coronary artery disease were injected with either 0.5 mg of atropine or saline before treadmill exercise echocardiography. HR response during and after exercise was recorded. Atropine resulted in a greater increase in HR before exercise (increase of 15 +/- 9 vs 5 +/- 7 beats per minute, P < 0.0001) and a higher HR rate during the first 5 minutes of exercise (P < 0.05). In recovery, there was an exponential decrease in HR in both atropine and control groups. However, at the end of image acquisition (66 +/- 15 seconds), the HR was higher in the atropine group (128 +/- 21 vs 115 +/- 19 beats per minute, P = 0.02) and remained higher throughout the 10-minute recovery period (P = 0.0015). Dry mouth was more common after atropine injection (P = 0.005); other side effects were similar. The extent and resolution of myocardial ischemia were comparable in both groups. Atropine injection before treadmill exercise echocardiography results in a higher HR during the acquisition of echocardiographic images; whether atropine could affect the diagnostic accuracy of tread mill exercise echocardiography requires further study.

Acetylcholine↗