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(C) Vancouver
General Hospital.
This monograph may not be reproduced without permission.
For further information, please contact a Pharmacist. |
NAME OF DRUG
aminophylline
CLASSIFICATION
Bronchodilator
ALTERNATE NAME
THEOPHYLLINE, ETHYLENEDIAMINE
INDICATIONS
- symptomatic treatment of reversible bronchoconstriction
RECONSTITUTION AND STABILITY
- stable at room temperature
- DO NOT use if crystals are present
COMPATIBILITY
- compatible with most commonly used IV solutions
- compatible via Y-site with
amikacin, calcium
gluconate, ceftazidime, dexamethasone, diphenhydramine, dopamine,
erythromycin, fluconazole, furosemide, heparin, hydrocortisone, labetalol,
levofloxacin, lidocaine, magnesium sulphate, methylprednisolone, metoclopramide,
metronidazole, morphine, MVI, nitroglycerin, piperacillin-tazobactam,
potassium chloride, potassium phosphate, propofol, ranitidine, sodium
bicarbonate
- incompatible with amiodarone, corticotropin, diltiazem,
dobutamine, epinephrine, hyaluronidase, hydralazine, hydroxyzine, insulin,
isoproterenol, levorphanol, meperidine, norepinephrine, ondansetron, prochlorperazine,
verapamil
ROUTES OF ADMINISTRATION
- IV intermittent - in 50-100 mL of compatible IV solution administered at a rate of 25
mg/minute
- IV infusion - in 500-1000 mL of compatible IV solution
- rate of administration depends on age and clinical condition (see dosage)
VH & HSC ADMINISTRATION POLICY
D - Direct IV route restricted to physicians. Nuclear medicine
technologists may administer direct IV under the supervision of a cardiologist
who must be immediately available but not necessarily in the same room at the
time the drug is being given.
Aminophylline may be administered by nuclear technologists provided that: 1) an
intravenous dose of 50-100mg aminophylline is employed to reverse the side effects of IV
persantine; 2) the patient is currently under ECG monitoring; 3) a physician is
immediately available; 4) a prescription is written and signed by the physician; and 5) full
resuscitative equipment is immediately available
H - The IV infusion administration rate must be controlled by an automated infusion
control device.
AMINOPHYLLINE INFUSION RATE CHART
Aminophylline 500 mg ( = 400 mg theophylline) in 500 mL D5W
Dose (mg/hr) |
Dose (mg/hr) |
Rate
(mL/hr) |
| Aminophylline |
Theophylline |
|
| 10 mg/hr |
8 mg/hr |
10 mL/hr |
|
15
|
12 |
15 |
| 20 |
16 |
20 |
| 25 |
20 |
25 |
| 30 |
24 |
30 |
| 35 |
28 |
35 |
| 40 |
32 |
40 |
| 45 |
36 |
45 |
| 50 |
40 |
50 |
| 55 |
44 |
55 |
| 60 |
48 |
60 |
| 65 |
52 |
65 |
| 70 |
56 |
70 |
| 75 |
60 |
75 |
| 80 |
64 |
80 |
DOSAGE
Loading Dose: Recommended rate 25 mg/minute
- Adults and children who have not received theophylline containing products within
previous 24 hours: 6 mg/kg aminophylline (4.7 mg/kg theophylline)
- Adults and children who have received theophylline containing products within 24
hours: reduce the loading dose by 50% (3mg/kg aminophylline)
Maintenance dose:
| Patient population |
Aminophylline infusion (mg/kg/hr) |
| Children 9 - 12 |
0.8 |
Adolescents 12 - 16
smokers
non-smokers |
0.8
0.6 |
Adults
smokers
non-smokers
Cardiac decompensation, cor pulmonale and/or liver dysfunction |
0.8
0.5
0.25 |
NOTE: dosage must be individualized by monitoring theophylline plasma concentration
POTENTIAL HAZARDS OF PARENTERAL ADMINISTRATION
- rapid IV administration may result in hypotension, syncope, cardiac arrest, and death
IMPORTANT IMPLICATIONS
- 400 mg theophylline is equivalent to 500 mg aminophylline
- therapeutic serum levels: 55-110 umol/L (10-20 mcg/mL)
- each 1.25 mg/kg aminophylline results in a plasma theophylline increase of approximately
11 umol/L (2 mcg/mL)
- adverse effects include anorexia, nausea, vomiting, restlessness, irritability,
insomnia, headache
- serious arrhythmias and convulsions may occur at levels greater than 193 umol/L (35
mcg/mL) and are often not preceded by less serious signs of toxicity
Rev. July 2006