Page 351 - Cardiac Nursing
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                                                                                C HAPTER 1 5 / Electrocardiography  327
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                                                                                               6 6 6
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                   B
                              ■ Figure 15-40 ECG effects of hypokalemia. (A) T waves are flattened in many leads; large U waves are best
                              seen in the V leads. (B) Large U waves of hypokalemia. This ECG also shows the typical pattern of acute cor
                              pulmonale with S wave in lead I, Q-wave and T-wave inversion in lead III (the S1, Q3, and T3 pattern of cor
                              pulmonale). (Courtesy of Dr. William Nelson, Denver, Colorado.)
                                                                       Drugs That Prolong the QT Interval
                      DRUG EFFECTS
                                                                       Many drugs can prolong the QT interval and lead to arrhythmias,
                   Many drugs can affect the ECG by altering ST segments, T waves,  specifically polymorphic ventricular tachycardia called torsades de
                   U waves, QT interval, and by causing various arrhythmias such as  pointes (see Chapter 16). It is beyond the scope of this chapter to
                   bradycardia, AV block, and torsades de pointes. The effects of  list all of these drugs, but among the more common drugs known
                   drugs on the ECG are not specific because similar changes can re-  to prolong the QT interval are: (1) class IA antiarrhythmics
                   sult from cardiac diseases or electrolyte imbalances. The presence  (quinidine, procainamide), (2) class III antiarrhythmics (amio-
                   of ECG changes does not necessarily indicate toxic levels of the  darone, ibutilide, dofetilide, sotalol), (3) many antipsychotic and
                   drug but rather represents the effects of the drug on myocardial de-  antidepressant drugs, (4) some antibiotics, (5) some sedatives and
                   polarization and repolarization. Some common drug effects are  anesthetic agents, and (6) some histamine blockers, and many
                                                                                         9
                   discussed here.                                     others. See Elizari et al. or go to www.torsades.org for a more
                                                                       complete list of these drugs. Figures 15-45 and 15-46 show ECG
                                                                       changes commonly due to drugs.
                   Digitalis
                   Therapeutic doses of digitalis cause several changes on the ECG  LONG QT SYNDROMES (LQTS)
                   including: (1) flattening of the T wave or T-wave inversion, (2)
                   concave depression of the ST segment, often described as “sag-  A long QT interval can be inherited or it can be acquired because
                   ging” or “scooped,” (3) shortening of the QT interval, (4) devel-  of drug therapy, hypokalemia, or hypomagnesemia. 20–22  Seven
                   opment or enlargement of U waves, and (5) PR interval prolon-  types of congenital LQTS have so far been identified involving
                   gation. 2,7,10  Figure 15-44 is an example of digitalis effect.  gene mutations that disrupt the function of various ion channels
                   Digitalis toxicity causes arrhythmias including sinus bradycardia  in the cardiac membrane, leading to repolarization abnormalities
                   or SA block, AV block, atrial tachycardia and atrial tachycardia  that manifest as a long QT interval on the ECG. 21–23  Patients
                   with block, junctional tachycardia, and several ventricular ar-  with LQTS have an increased risk of sudden cardiac death and are at
                   rhythmias. See Chapter 16 for discussion of arrhythmias.  risk for developing torsades de pointes, a polymorphic ventricular
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