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Percutaneous tracheostomy may not be more effective than open technique
EDITOR We disagree with Stott's assertion that the incidence of
complications has been shown to be lower with percutaneous tracheostomy than with open surgical techniques. The paper quoted in support of this
statement Stott fails to mention Dulguerov et al's meta-analysis reported in
1999, which showed that percutaneous tracheostomy is associated with a
higher prevalence of certain complications.3 Their
comparison of recent surgical tracheostomy trials (n=21; 3512 patients)
and percutaneous tracheostomy trials (n=27; 1817 patients) shows that perioperative complications are more common with the percutaneous technique (10% v 3%), whereas postoperative complications
occur more often with the surgical technique (10% v 7%).
The bulk of the differences is in minor complications, except
perioperative death (0.44% v 0.03%) and serious
cardiorespiratory events (0.33% v 0.06%), which were much
higher with the percutaneous technique. These authors also noted
significantly fewer complications in recent studies compared with older ones.
In the present state of knowledge it would seem unethical to mount a
large double blind trial comparing the two techniques as this would
subject about a quarter of patients, who would usually be deemed
unsuitable for a percutaneous technique, to an increased risk of
complications. It is likely that such patients will continue to be
referred for open tracheostomy. While this selection bias continues, it
is misguided to state that percutaneous tracheostomy holds fewer risks
than the open technique.
In his review of recent advances in intensive care Stott
emphasised the efficacy of percutaneous tracheostomy over the
conventional open surgical approach.1 We agree that
percutaneous tracheostomy may indeed be the preferred method in
selected cases, but it is invariably not used in patients who present
anatomical challenges such as a short, thick neck; goitre; a history of
neck surgery; or a concurrent coagulopathy. Such difficult cases
probably represent about a quarter of an average population requiring tracheostomy.
by Hill et al
describes the results of 356 percutaneous procedures performed in a single unit over four years.2 No direct comparison is made with open tracheostomies, and the authors do
not report the numbers and type of patients deemed unsuitable for
percutaneous tracheostomy and referred for open procedures. The six
previous independent series quoted that detailed complication rates for
open tracheostomy were published on average nearly 20 years earlier,
and a conclusion was reached by comparison with these older studies.
David Howard
Royal National Throat, Nose and Ear Hospital, London WC1X 8DA
| 1. |
Stott S.
Recent advances in intensive care.
BMJ
2000;
320:
358-361 |
| 2. | Hill BB, Zweng TN, Maley RH, Charash WE, Toursarkissian B, Kearney PA. Percutaneous dilatational tracheostomy: report of 356 cases. J Trauma 1996; 41: 238-243[Medline]. |
| 3. | Dulguerov P, Gysin C, Perneger TV, Chevrolet JC. Percutaneous or surgical tracheostomy: a meta-analysis. Crit Care Med 1999; 27: 1617-1625[CrossRef][Medline]. |
Author's reply
EDITOR The meta-analysis referenced looks only at studies published up to 1996 and compares four different percutaneous techniques with surgical
tracheostomies performed in two different eras.1 As most
of the deaths occurring with percutaneous tracheostomy occur with a
non-dilatational technique it would seem prudent to exclude these from
the analysis.
There have been three published prospective trials comparing
dilatational percutaneous tracheostomy with open surgical
techniques.2-4 These show complication rates for
percutaneous tracheostomy to be as low as or lower than those for the
surgical technique. This, coupled with the reduced cost, avoidance of
moving critically ill patients, and low long term complication rates,
means that I can still conclude that percutaneous tracheostomy is a
significant recent advance.
More still needs to be known about immunonutrition
EDITOR The question of immunonutrition is complex, and the different nutrients
used in clinical trials can have different, and opposing, effects on
the immune system. For example, L-arginine and glutamine stimulate a variety of immune functions.2 In contrast,
omega 3 and omega 6 fatty acids inhibit a variety of immune
functions.
2 3
The timing of administration of these nutrients may therefore be
critically important: although it is generally believed that stimulation of the immune system is beneficial in critically ill patients, this may not always be the case. For example, in certain patients (those with adult respiratory distress syndrome or multiorgan failure) in whom the cytokine cascade and production of inflammatory mediators has been suggested to be excessive, administration of omega 3 and omega 6 fatty acids would be beneficial in reducing production of
these mediators.
In terms of immunonutrition affecting clinical outcome in critical
illness, a recent critical analysis of all the randomised controlled
trials in which L-glutamine was given found little evidence
to support its routine clinical use.4 A recent
meta-analysis found that giving combinations of immunomodulatory
nutrients reduced infectious complications but not
mortality.5
When the use of nutrition in critically ill patients is being
considered, these considerations must be taken into account. It is
still not clear which patients will benefit from being fed these
immunomodulatory nutrients and which may not.
Brookes and Howard's point that not all patients are suitable
for a percutaneous tracheostomy is well made, but the figure quoted of
25% is conjecture and not referenced. As I cannot find any data to
produce a figure of my own I will not, but I do question their final
paragraph when they state that because of this figure a double blind
trial would be unethical. This is curious as nowhere in my article did
I suggest that one should be performed.
Grampian University Hospitals Trust, Aberdeen AB25 2ZN
s.a.stott{at}abdn.ac.uk
1.
Dulguerov P, Gysin C, Perneger TV, Chevrolet JC.
Percutaneous or surgical tracheostomy: a meta-analysis.
Crit Care Med
1999;
27:
1617-1625.
2.
Hazard P, Jones C, Benitone J.
Comparative clinical trial of standard operative tracheostomy with percutaneous tracheostomy.
Crit Care Med
1991;
19:
1018-1024[Medline].
3.
Crofts SL, Alzeer A, McGuire GP, Wong DT, Charles D.
A comparison of percutaneous and operative tracheostomies in intensive care patients.
Can J Anaesth
1995;
42:
775-779 4.
Friedman Y, Fides J, Mizock B, Samuel J, Patel S, Appavu S, et al.
Comparison of percutaneous and surgical tracheostomies.
Chest
1996;
110:
480-485
I have concerns over one section in Stott's article on recent
advances in intensive care.1 These concerns relate to the
paragraphs on nutrition, and particularly the key points box on page
358; there it is stated that recent work has shown that omega 3 polyunsaturated fatty acids improve mortality in critical illness.
University of Aberdeen, Aberdeen AB24 3UX
s.d.heys{at}abdn.ac.uk
1.
Stott S.
Recent advances in intensive care.
BMJ
2000;
320:
358-361. (5 February.)
2.
Heys SD, Gough DB, Khan L, Eremin O.
Nutritional pharmacology and malignant disease: a therapeutic modality.
Br J Surg
1996;
83:
608-619[Medline].
3.
Almallah YZ, El-Tahir A, Heys SD, Richardson S, Eremin O.
Distal procto-colitis and n-3 polyunsaturated fatty acids: the mechanism(s) of natural cytotoxicity inhibition.
Eur J Clin Invest
2000;
30:
58-65[Medline].
4.
Heys SD, Ashkanani F.
Glutamine.
Br J Surg
1999;
86:
289-290[CrossRef][Medline].
5.
Heys SD, Walker LG, Smith I, Eremin O.
Enteral nutritional supplementation with key nutrients in patients with critical illness and cancer: a meta-analysis of randomized controlled clinical trials.
Ann Surg
1999;
229:
467-477[CrossRef][Medline].
© BMJ 2000
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