[back] Paracetamol Fever
Why anyone, with any flu, would be an idiot to take Paracetamol
First of all, look at this:
Now why might this be?
Well, it's pretty simple, but the problem is that the only two studies which point to the why, were done in Saudi Arabia in the 1990's. And no, no-one's done anything after that to confirm this, as per their usual "You cannot say anything until we've spent 80 years, doing 200 studies,..." :blah: :blah:
So having not bothered to do ANY studies at all... ( at least, I can't find any) paracetamol continues to be recommended on a totally unscientific basis.
And really, why would we be surprised?
The reasons why paracetamol is dangerous in infections are in these two studies attached.
To try to explain to you in simple terms here is why.
acetaminophen/paracetamol/tylenol paralyses polymorphonuclear leukocytes.
Polymorphonuclear leukocytes are the first cells to arrive at sites of infection and play a crucial role against bacterial, viral, fungal and parasitic infections. They increase oxidative strategies by the body to kill pathogens by using the ability to make hydrogen peroxide in the body and hydroxyl radicals. These metabolites have a very powerful bactericidal effect. BUT not only does paracetamol inhibit the formation of these metabolites, paracetamol scavenges HOCL and thus paralyses the MPO-H202-Cl- antimicrobial system of the front line neutrophils.
So when you take paracetamol, the paracetamol opens the door and says to influenza, meningitis, whatever... "Welcome, enter, do your flipping worst, for the paracetamol will now prevent the body's natural protection system from working properly."
What's the bet that most of the swineflu, any flu deaths, have taken paracetamol? Of course, because that's what the doctor, the health department tells you to do. And the father of the med student who died of meningitis said just that too didn't he? "Take paracetamol and see a doctor... " and that paracetamol might just have been the difference between surviving and dying... who knows? Scientists sure don't, because they continue to refuse to look at the very evidence in front of their eyes.
That's the first article.
The second article attached shows that the HIGHER the temperature you have the MORE paracetamol INHIBITS neutrophils and prevents phagocytes from engulfing and dealing with the pathogen.
So why would any doctor, in their right mind prescribe paracetamol?
You tell me, and then we'll both know.
NOTE WHO's first reference, which is this:
Paracetamol: use in children
Frank Shann, Intensive Care Unit, Royal Children's Hospital, Melbourne
It is sensible to use paracetamol to reduce the discomfort caused by minor acute infections, surgical procedures and triple antigen. It is also sensible to use paracetamol to reduce fever in patients with cardiac or respiratory failure. However, there is little evidence to support the use of paracetamol to treat fever in patients without heart or lung disease, or to prevent febrile convulsions. Paracetamol may prolong infection and reduce the antibody response in mild disease, and increase morbidity and mortality in severe infection. The dose in children is 10-15 mg/kg 4 hourly, to a maximum of 100mg/kg/day, and no patient should receive more than 4 g/day.
Key words: fever, pain, analgesia, antipyretic
(Aust Prescr 1995;18:33-5)
Despite the widespread use of paracetamol, there is still confusion about when it should be used and the correct dose.1
Indications for paracetamol
In patients with cardiac or respiratory failure who are febrile, it can be helpful to give paracetamol to reduce oxygen consumption, carbon dioxide production and cardiac output. However, in patients without heart or lung disease, fever is harmful only at temperatures over 41oC. Such high temperatures are usually caused by heat stroke or brain injury2, and, if so, they do not respond to paracetamol or aspirin.
There is no evidence that antipyretics prevent febrile convulsions; this is probably because the convulsion is caused by the rapid rise in temperature that usually occurs at the beginning of an illness.2
There are no controlled trials comparing an antipyretic to placebo for febrile convulsions, but one study comparing phenobarbitone plus antipyretic to placebo plus antipyretic found a high risk of febrile convulsions in the placebo plus antipyretic group, suggesting that antipyretic therapy did not protect against convulsions.3
In a recent controlled trial in children who had had a febrile convulsion4, children given paracetamol 15-20 mg/kg every 4 hours were just as likely to have another convulsion as children given paracetamol only when their rectal temperature exceeded 37.9oC.
It is sensible to give paracetamol to reduce the unpleasant symptoms caused by mild acute infections. However, paracetamol does not have a dramatic effect: a recent controlled trial5 found that paracetamol caused only a modest improvement in activity and alertness in children with acute infection, and that there was no significant improvement in mood, comfort, appet ite or fluid intake. Because many patients with infection have fever and discomfort, it is often assumed that fever causes discomfort but strenuous exercise causes temperatures up to 40oC without causing discomfort.
Triple antigen reactions
Two studies6,7 have shown that paracetamol reduces fever and abnormal behaviour in children who have had triple antigen injection. A third study8 found that paracetamol had no significant effect, but only one dose of 10 mg/kg of paracetamol was given 4 hours after immunisation. A reduction in adverse reactions to triple antigen is likely to improve immunisation rates.
There has been little systematic study of the use of paracetamol for postoperative pain, but controlled trials of nonsteroidal antiinflammatory drugs9 and experience with paracetamol suggest that paracetamol provides adequate analgesia for minor surgery, and allows a reduced dose of opiates after major surgery. Paracetamol should probably be given before surgery, rather than waiting for pain to develop after surgery.9
The dose of paracetamol
While a single dose of 5 mg/kg of paracetamol results in some reduction in the temperature of febrile children, there is a much larger fall with 10 mg/kg and an even larger and more prolonged fall with 20 mg/kg.10
The maintenance dose of paracetamol in children is 10-15 mg/kg 4 hourly10, to a maximum of 100 mg/kg/day, and no patient should receive more than 4 g/day. An initial dose of 20 mg/kg can be given if it is felt that maximum effect is needed quickly. A dose of 30 mg/kg 8 hourly gives levels in the therapeutic range.10 A single dose of 30 mg/kg of paracetamol at bedtime can increase the amount of sleep for the whole family when a child has mild acute infection, but the danger of repeating this dose has to be emphasised.
In Australia, paracetamol is sold in preparations containing 60mg in 0.6 mL (or 100 mg/mL), 100 mg/mL, 50 mg/mL, 120 mg in 5 mL (or 24 mg/mL) and 240 mg in 5 mL (or 48 mg/mL). It is difficult to calculate a dose of 15 mg/kg from these formulations. Parents often give a very low dose of paracetamol because they use the infant dropper, designed for 100 mg/mL preparations, to measure a dose of the more dilute preparations designed for use in older children.10
Liquid preparations of paracetamol are expensive, with the MIMS price varying from $1.11 to $5.39 per g of paracetamol (mean $2.52 per g). In contrast, the MIMS price of 500 mg tablets of paracetamol is 10c to 45c per g. Tablets are a much cheaper form of paracetamol than liquid preparations, and some brands of paracetamol tablets are very much cheaper than others (the brands listed in the Schedule of Pharmaceutical Benefits tend to be less expensive).
Antipyretics may be harmful
Too many parents and health workers think that infection is bad, infection causes fever, and that therefore fever is bad. In fact, fever is often a beneficial host response to infection, and moderate fever improves immunity.11
Therefore, it may not be a good idea to give drugs that reduce temperature to patients with severe infection.
I have recently reviewed 1 the results of 9 controlled trials in mammals of the effect of paracetamol or aspirin on mortality or virus excretion.
Four trials found that aspirin increased mortality in bacterial or viral infection.
Viral shedding was increased by paracetamol or aspirin in 3 studies, possibly increased in one, and not affected in two (one used only pharyngeal washings, and one had only 9 subjects in the aspirin and placebo groups).
One study found that antibody production was impaired by both paracetamol and aspirin, but no effect on antibody production was detected in the study with only 9 subjects in the aspirin and placebo groups.
This evidence suggests that aspirin and paracetamol increase mortality in severe infection, and that they may prolong the infection and reduce the antibody response in mild disease.
Despite the millions of children treated with paracetamol, very little serious toxicity has been recognised (but note that the association between aspirin and Reye's syndrome was not recognised for many years). Penna and Buchanan 12 reviewed reports of 7 deaths and 11 cases of hepatotoxicity associated with paracetamol in children. The children who died had had more than 300 mg/kg/day of paracetamol for 1-6 days, except for one child where the plasma level suggested that the actual dose may have been much higher than the reported dose. The children who had hepatotoxicity but survived had all had 150 mg/kg/day for 2-8 days, except for two children where there was a discrepancy between the low reported doses and the high plasma levels of paracetamol (which was probably due to miscalculation of the dose or deliberate poisoning). Presumably, other cases of paracetamol toxicity in children have occurred and have gone unrecognised or unreported, but the evidence suggests that toxicity from paracetamol is rare with doses less than 150mg/kg/day. The dose of paracetamol should not exceed 100mg/kg/day in children, and no patient should receive more than 4 g/day.
In acute poisoning from paracetamol, treatment with acetylcysteine should be started within 10 hours if possible. If the delay in starting acetylcysteine is more than 10 hours or if there is established liver failure, a longer course of acetylcysteine should be given.13,14 The best regimen has not been determined; I suggest giving 150 mg/kg of acetylcysteine in 5% dextrose intravenously over 15 minutes; then 12mg/kg/hour (200 microgram/kg/minute) for 4 hours; then 6mg/kg/hour (100 microgram/kg/minute) for at least 16 hours if the delay in starting was less than 10 hours, for at least 28 hours if the delay was 10-16 hours and at least 68 hours if the delay was more than 16 hours. Acetylcysteine should be continued as long as the patient has encephalopathy, abnormal liver function tests or paracetamol detected in the serum.
The antipyretic action of paracetamol is useful in febrile patients with cardiac or respiratory failure. The analgesic action is useful in minor acute infection, for postoperative pain and after vaccination with triple antigen.
There is little evidence to support the use of paracetamol to treat fever in patients without heart or lung disease, or to prevent febrile convulsions. Indeed, paracetamol may decrease the antibody response to infection, and increase morbidity and mortality in severe infection. It should be explained to parents that fever is usually a helpful response to infection, and that paracetamol should be used to reduce discomfort, but not to treat fever.
Although an initial dose of 20 mg/kg of paracetamol can be given, this is rarely necessary. The maintenance dose in children is 10-15 mg/kg 4 hourly. Hepatotoxicity has been reported with doses of 150 mg/kg/day, and no patient should be given more than 100 mg/kg/day (up to a maximum of 4 g/day).
1. Shann F. Paracetamol: when, why and how much [editorial; comment]. J Paediatr Child Health 1993;29:84-5.
2. Schmitt BD. Fever in childhood. Pediatrics 1984;74:929-36.
3. Camfield PR, Camfield CS, Shapiro SH, Cummings C. The first febrile seizureantipyretic instruction plus either phenobarbital or placebo to prevent recurrence. J Pediatr 1980;97:16-21.
4. Schnaiderman D, Lahat E, Sheefer T, Aladjem M. Antipyretic effectiveness of acetaminophen in febrile seizures: ongoing prophylaxis versus sporadic usage. Eur J Pediatr 1993;152:747-9.
5. Kramer MS, Naimark LE, RobertsBrauer R, McDougall A, Leduc DG. Risks and benefits of paracetamol antipyresis in young children with fever of presumed viral origin [see comments]. Lancet 1991;337:591-4. Comments in: Lancet 1991;337:1045,1347-8.
6. Ipp MM, Gold R, Greenberg S, Goldbach M, Kupfert BB, Lloyd DD, et al. Acetaminophen prophylaxis of adverse reactions following vaccination of infants with diphtheriapertussistetanus toxoidspolio vaccine. Pediatr Infect Dis J 1987;6:721-5.
7. Lewis K, Cherry JD, Sachs MH, Woo DB, Hamilton RC, Tarle JM, et al. The effect of prophylactic acetaminophen administration on reactions to DTP vaccination. Am J Dis Child 1988;142:62-5.
8. Uhari M, Hietala J, Viljanen MK. Effect of prophylactic acetaminophen administration on reaction to DTP vaccination. Acta Paediatr Scand 1988;77:747-51.
9. Dahl JB, Kehlet H. Nonsteroidal antiinflammatory drugs: rationale for use in severe postoperative pain [see comments]. Br J Anaesth 1991;66:703-12. Comment in: Br J Anaesth 1992;68:118.
10. Shann F. Paracetamol and fever. Aust Pharm 1991;10:217-20.
11. Roberts NJ Jr. Impact of temperature elevation on immunologic defenses. Rev Infect Dis 1991;13:462-72.
12. Penna A, Buchanan N. Paracetamol poisoning in children and hepatotoxicity. Br J Clin Pharmacol 1991;32:143-9.
13. Smilkstein MJ, Knapp GL, Kulig KW, Rumack BH. Efficacy of oral Nacetylcysteine in the treatment of acetaminophen overdose. Analysis of the national multicenter study (1976 to 1985) [see comments]. N Engl J Med 1988;319:1557-62. Comment in: N Engl J Med 1989;320:1417-8.
14. Keays R, Harrison PM, Wendon JA, Forbes A, Gove C, Alexander GJ, et al. Intravenous acetylcysteine in paracetamol induced fulminant hepatic failure: a prospective controlled trial. Br Med J 1991;303:1026-9.
This article has been reprinted (with minor modifications) from the Journal of Paediatrics and Child Health 1993;29:84-5.