I've visited this issue before (ref 1) and still remain to be
convinced that long-chain superglues are less 'toxic' than short-chain DIY
superglues, given that no superglue should ever be placed in a wound. The
exothermic and the cyanate components of the argument are also completely
overstated; millions get superglue on their fingers everyday and dont feel
the heat or keel over with cyanide toxicity!
I've visited this issue before (ref 1) and still remain to be
convinced that long-chain superglues are less 'toxic' than short-chain DIY
superglues, given that no superglue should ever be placed in a wound. The
exothermic and the cyanate components of the argument are also completely
overstated; millions get superglue on their fingers everyday and dont feel
the heat or keel over with cyanide toxicity!
I'm afraid it's all a classic marketing ploy. Create something
different, shroud it with high-flying properties, degrade the competition,
say it is expensive to produce and then sell it for a fortune. And dont
forget to make it single-use (even though nothing can conceivably grow or
multiply in such a medium).
The sad part? Millions of children whose wounds could safely be
treated with a drop of cheap, short-chain DIY superglue (properly and
appropriately applied) are deprived of the treatment modality because
articles such as the above endlessly and unscientifically propogate the
myth.
1. Full-thickness skin necrosis of the fingertip after application of
superglue
DaCruz D
The Journal of Hand Surgery
January 2004 (Vol. 29, Issue 1, Page 159)
“Trials are nothing like real life” is a complaint that defines a
common problem in the practice of evidence-based medicine. Differences
between patient populations or the circumstances of trials and real life
often leave us bewildered when trying to determine the applicability of
clinical research to the care of our own patients. Sometimes inclusion
and exclusion criteria for subjects in trials mean t...
“Trials are nothing like real life” is a complaint that defines a
common problem in the practice of evidence-based medicine. Differences
between patient populations or the circumstances of trials and real life
often leave us bewildered when trying to determine the applicability of
clinical research to the care of our own patients. Sometimes inclusion
and exclusion criteria for subjects in trials mean that our own patients
would never have received a treatment of interest. In other cases the way
in which the treatment was delivered could not be replicated in our own
practice. Alternatively, the outcomes reported in a trial only partly
reflect outcomes of interest to our patients. Sometimes we can find
evidence but the methodological validity of that evidence is poor, causing
us to question the reliability of the results. In order to make a
pragmatic decision in the real world, we must resolve these uncertainties
if we are to make use of the evidence available and take decisions about
the clinical care of patients.
Rather than do this on the basis of a hunch or a gut feeling, Mike
Clancy has developed a remarkably useful and intuitive graphical
representation of the “fit” of the evidence to a patient’s problems
presented in the articles: A new way of demonstrating how close the
evidence is to the question you asked and In patients with head injury
undergoing rapid sequence intubation, does pre-treatment with intravenous
lignocaine/lidocaine lead to an improved neurological outcome? A review
of the literature.
In my opinion this graphical representation is as powerful as the
forest plots used to depict the results of meta analyses. With one simple
graphic, Clancy has devised a method for illustrating how well or how
badly the evidence fits the question at hand. I would suggest that the
area encompassed by the rhombus created in these graphs could be used to
provide a weighting score for individual articles, with the smallest area
representing the best fit. I consider this a major advance in the
practice of evidence-based medicine and one that I will certainly adopt
when teaching critical appraisal and the difficult step from the completed
critical appraisal to the application of evidence. Thank you Mr Clancy!
I presume that Dr Fairhurst is referring to a substance used
ubiquitously in the Antipodes and more commonly spelled 'methoxyflurANE'.
It is estimated that over three million doses have been used over the
last 25 years in Australia (Jacobs, 2010). It is used by state ambulance
services in the pre-hospital environment in most states of Australia, by
the Australian Defence Forces, within emergency de...
I presume that Dr Fairhurst is referring to a substance used
ubiquitously in the Antipodes and more commonly spelled 'methoxyflurANE'.
It is estimated that over three million doses have been used over the
last 25 years in Australia (Jacobs, 2010). It is used by state ambulance
services in the pre-hospital environment in most states of Australia, by
the Australian Defence Forces, within emergency departments, on adults and
children, by St John's Ambulance and by the Surf Life Saving Association.
In May of 2010, it was added to the Pharmaceutical Benefits Scheme in
Australia, to be included in the GP 'Doctor's Bag List' (NPS, 2010).
Methoxyflurane did not have its license renewed in Europe and the USA
(it was not withdrawn) because of justifiable concerns regarding
nephropathy in anaesthetic doses. These are several orders of magnitude
different to those currently used for analgesic purposes in Australia.
Methoxyflurane is not an alternative to opiate analgesia, rather an
efficient and safe bridging agent that can be used prior to administration
of more definitive agents. It is therefore more akin to Entonox than
intranasal opiates, albeit more portable and easier to administer in
austere environments.
There are a number of situations where methoxyflurane is ideal. It
does not require IV access, which can be limited in patients with
trypanophobia, difficult vascular access, or those being treated by
providers not qualified to administer parenteral agents. It has been shown
to be of great utility in the past in dressing changes, particularly those
associated with burns. It could be an ideal agent in the mass casualty
incident scenario. It has a small volume, is significantly more portable
than Entonox, is neither flammable nor explosive, can be self-
administered, and can last up to an hour. It has been proposed by as a
suitable agent for the battlefield (McClellan, 2007).
As Dr Fairhurst indicates, it is almost inevitable that a "clinical
trial" in the UK will be required to reiterate what is already known in
Australia; that there is an abundance of experience that already exists to
suggest that methoxyflurane can be used, and is used, as an effective and
safe analgesic in the acute care environment.
References
Jacobs I. Health effects of patients given methoxyflurane in the pre-
hospital setting: A data linkage study. The Open Emergency Medicine
Journal 2010 (3) 7-13
NPS. Methoxyflurane (Penthrox) for analgesia (doctor's bag listing)
Available at
http://www.nps.org.au/health_professionals/publications/nps_radar/2010/may_2010/methoxyflurane?SQ_BACKEND_PAGE=main&backend_section=am&am_section=edit_asset&assetid=86209&asset_ei_screen=contents&sq_link_path=,0,165622,93,526,164474,148952,170094,170085&sq_asset_path=1,43,72,360,686,25055,86207,86208#fnote12,
Accessed June 6th, 2010.
McLennan JV. Is methoxyflurane a suitable battlefield analgesic? J R
Army Med Corps. 2007 Jun;153(2):111-3.
We read with interest the article by Chen et al which
demonstrated that a MEDS score greater than 12 may
be discriminant for Emergency Department (ED) triage,
ICU placement (1). These results of importance are in
accordance with those of our group. We prospectively
evaluated the accuracy of the MEDS score in 286
patients with documented sepsis admitted into our
medical ICU (10 beds) after an ED cons...
We read with interest the article by Chen et al which
demonstrated that a MEDS score greater than 12 may
be discriminant for Emergency Department (ED) triage,
ICU placement (1). These results of importance are in
accordance with those of our group. We prospectively
evaluated the accuracy of the MEDS score in 286
patients with documented sepsis admitted into our
medical ICU (10 beds) after an ED consultation and we
compared it with the performance of the SAPS II score
calculated with the worst values of physiologic
variables during the first 24 hr of ICU admission. The
median age (interquartile) was 69 yr (52.1-78.8), for a
median MEDS value of 10 (8-12) and a SAPS II score of
51 (35.7-70). Community-acquired pneumonia was the
main source of sepsis (58.6%).
In our series, the two scores discriminate well between
survivors and non- survivors (in-hospital mortality rate:
32.9%) if we consider the area under the ROC curve
which was 0.771 [95% confidence interval (CI),
0.714-0.828) for the MEDS score and 0.830 (95%CI,
0.781-0.880) for the SAPS II score. Furthermore,
severity of illness, age, and mortality increased when
stratifying patients into the five risk groups defined by
Shapiro et al (p<. 000.1) (see table) (2). Whereas, Chen
et al reported an increased mortality in case of MEDS
score > 12 [calculated odds ratio (OR): 4.51], in our
population a cut-off value of 10 was already an
important predictor of death: OR, 5.4(95%CI: 3.01-9.72),
sensitivity 0.475, specificity 0.857, positive predictive
value 0.809, negative predictive value 0.562.
As in Chen et al cohort, the MEDS score performs well
and then may be an appropriate tool in identification of
ED patients at high risks of death from sepsis.
However, its usefulness should be tested in surgical
ICU patients and prospectively evaluated in the ED to
decide ICU admission.
Table 1
MEDS score
Patients (n)
Age (yr)
SAPSII
Hospital mortality (%)
0-4
19
44.6 ± 16
31.8 ± 16.7
5.3
5-7
44
50 ± 14.4
36.9 ± 16.2
9.1
8-11
137
65.4 ± 18.6
52 ± 20
27.7
12-15
56
75.8 ± 10.6
65.8 ± 21
50.8
>15
30
78.3 ± 10.9
77.5 ± 22.6
76.7
References
1 Chen CC, Chong CF, Liu YL, et al. Risk stratification
of severe sepsis patients in the emergency
department. Emerg Med J 2006; 23: 281-5
2 Shapiro NI, Wolfe RE, Moore RB, et al. Mortality in
Emergency Department Sepsis (MEDS) score: a
prospectively derivated and validated clinical prediction
rule. Crit Care Med 2003; 31:670-5
I read the study with interest but felt that there was no way of
knowing what type of patient cases the productivity was being based on.
By this I mean that it is very possible that the SHOs and FY2s saw
different cases mixes, ie one saw more simple minor injuries than the
other. Also I could not see a mention as to the varying experiences of
the FY2s and SHOs, were the SHOs all first year SHOs and had some of them
no...
I read the study with interest but felt that there was no way of
knowing what type of patient cases the productivity was being based on.
By this I mean that it is very possible that the SHOs and FY2s saw
different cases mixes, ie one saw more simple minor injuries than the
other. Also I could not see a mention as to the varying experiences of
the FY2s and SHOs, were the SHOs all first year SHOs and had some of them
not even done an FY2 year?
Are 'operative findings' a gold standard for diagnosis of a septic
joint? Discussion of interpretation of synovial fluid in Roberts: Clinical
Procedures in Emergency Medicine, 4th ed, suggests that gout, pseudogout
and other arthritides can give turbid fluid.
This clearly has a major impact on interpretation of the data.
I found this article which showed suboptimal use of chaperones in
emergency departments to be of great interest. In my clinical work in
primary care in the UK, I often struggle with providing a chaperone for
intimate examinations. The two main issues I have are who we should bring
in, and what should they see.
Firstly I feel that the person brought in should be someone who is
allowed to examine patients themsel...
I found this article which showed suboptimal use of chaperones in
emergency departments to be of great interest. In my clinical work in
primary care in the UK, I often struggle with providing a chaperone for
intimate examinations. The two main issues I have are who we should bring
in, and what should they see.
Firstly I feel that the person brought in should be someone who is
allowed to examine patients themselves. The presence of a nurse would be
much better than that of a receptionist. I am not sure it is acceptable to
the patient or the non-clinical member of staff for someone non-clinical
to observe the patient in a state of undress. However in most practices
nurses are very busy-they are not waiting around to be called upon to
chaperone when necessary. They have their own patient lists, as do we. The
delay involved waiting for a nurse to become available impacts
significantly on the patients waiting for both nurse and doctor.
Secondly what should the chaperone see? The idea, as I understand it,
is that their presence protects the patient from a doctor doing something
inappropriate to the patient, but also as a protection for the doctor in
case the patient alleges that the doctor did something wrong. This
necessitates that they witness the examination explicitly--it is not
enough then for them to be in the same room behind a curtain.
I feel that the current concepts regarding chaperone use need to be
revised. Perhaps clearer guidance should be developed that is more
practical for everyday clinical practice, both in primary and secondary
care.
The LOW COST RES-Q-SCOPE(R) where digital video technology makes life
a little easier.
The patented and FDA Registered RES-Q-SCOPE(R)is readily available and
considered essential in the emergency field, where the emergency needs to
be dealt with quickly and effectively. The situations commonly found more
frecuently by Paramedics, Medics in the military, First respo...
The LOW COST RES-Q-SCOPE(R) where digital video technology makes life
a little easier.
The patented and FDA Registered RES-Q-SCOPE(R)is readily available and
considered essential in the emergency field, where the emergency needs to
be dealt with quickly and effectively. The situations commonly found more
frecuently by Paramedics, Medics in the military, First responders, Rescue
Units, mass casualties personnel and the Emergency Room. The RES-Q-
SCOPE(R) stands to the challenge and is readily available at very low
cost. A state of the art Hand Held FIELD VIDEO LARYNGOSCOPE, a low cost
self contained, self powered device, with disposability advantages which
enables rapid serial intubations in the field. The RES-Q-SCOPE(R) is the
only Laryngoscope in the world which is designed to avoid free hand ET
uncertainty by actually PRE-LOADING A STANDARD ENDOTRACHEAL TUBE 6-8.5 mm
prior to intubation.
The RES-Q-SCOPE (R) is a patented and FDA Registered and Listed,
multi-function field video laryngoscope, which uses cutting edge digital
image technology featuring a multiple positional colour 2.75" LCD screen to
externally visualize the intubation process in the field. The RES-Q-SCOPE
(R) requires modest learning curve, to slide the device into position to
visualize the epiglottis with little effort. The RES-Q-SCOPE(R) is spine
injury friendly with minimal need, if any, to re-position the C-spine in
case of suspected neck injury. Further, the RES-Q-SCOPE (R) itself,
features a channel where a standard endotracheal tube can be easily pre-
loaded into the device. SHORT AND OBESE NECKS MAKE LITTLE DIFFERENCE WHEN
USING THE RES-Q-SCOPE(R). A light source for external visualization of the
intubation process, as the endotracheal tube passes into the trachea. The
process can be seen through a small colour LCD screen, which has the
ability to adopt multiple positions, so that the PRACTITONEAR CAN BE
LOCATED AT THE SIDE OF THE PATIENT OR AT MULTIPLE OTHER POSITIONS AROUND
THE PATIENT. A vacuum source can be attached to an external adaptor
provided, to assist clearing fluids that may be present in the throat. The
same channel can be reversibly, used to provide oxygen if needed. A
disposable unit can be easily detached and discarded. Thus, multiple clean
intubations, may be performed in the field in a very short time span. The
simple attachment of a new disposable unit allows very rapid serial
intubation of multiple patients in a disaster theatre or emergency scene.
The RES-Q-SCOPE (R) is powered with a rechargeable LiOn long duration
battery, also allowing for serial intubations when needed. Additionally an
emergency dry cell pack is also available using 4 AA's to power the unit
under extreme conditions such as combat settings.
The RES-Q-SCOPE(R) is a product designed to improve the chances of
saving a life in a respiratory emergency where it occurs, in the field. It
is considered essential in disaster preparation and emergency response of
all kinds including combat emergencies. Complete information, description
and video of conscious intubation can be obtained by visiting http://www.res-q-
tech-na.com (a full kit may cost between $400 t0 $500 USD).
Indeed we are indebted to Dr. Ayrik for his comments on one of the
most
dramatic cardiovascular emergencies: aortic dissection.
He rightly points out, that acute aortic dissection may not always present
with
the classical cardinal symptoms, particularly the sudden, sharp and
tearing
pain. Moreover, the author states that 10 % of aortic dissections are
painless
and he warns that the diagnosis ca...
Indeed we are indebted to Dr. Ayrik for his comments on one of the
most
dramatic cardiovascular emergencies: aortic dissection.
He rightly points out, that acute aortic dissection may not always present
with
the classical cardinal symptoms, particularly the sudden, sharp and
tearing
pain. Moreover, the author states that 10 % of aortic dissections are
painless
and he warns that the diagnosis can be missed in the absence of the
classic
pattern, and that atypical presentation needs a high index of suspicion to make the right diagnosis.
From my personal experience in a huge cardiac centre I completely agree
with
all these statements. However, I should like to add that there is a group
of
patients who are at particular risk for such an atypical presentation: the patients with Marfan syndrome.
Aortic dissection is the most endangering clinical finding in this
particular
patient group, typically occurring - with or without previous aortic root
dilatation - after the second decade of life and only infrequently during
childhood and adolescence. Precisely in Marfan patients, not infrequently
symptoms from acute dissection may be atypical and severe pain may be
completely missed. Therefore, any acute deterioration in Marfan patients
necessitates the exclusion of an acute aortic dissection.
Harald Kaemmerer, MD, VMD, PhD
Address for correspondence:
Harald Kaemmerer, M.D., V.M.D., PhD, FESC
Deutsches Herzzentrum München
Klinik für Kinderkardiologie und angeborene Herzfehler
Lazarettstr. 36, 80636 München, Germany
Phone: +49-89-1218-3011
Fax: +49-89-1218-3013
Email: Kaemmerer@dhm.mhn.de
References
Kaemmerer H, Oechslin E, Seidel H, Neuhann T, Neuhann IM, Mayer HM, Hess
J. Marfan syndrome: what internists and pediatric or adult cardiologists
need
to know. Expert Rev Cardiovasc Ther. 2005 Sep; 3(5): 891-909.
It is interesting to once again read an article comparing the abilities of
anaesthetic vs. emergency department staff to perform RSI.
Unfortunately, I feel this article has been tarnished by two areas of
bias.
The first area is considered under 'time to RSI'. The emergency physicians
intubated 94% of patients within 15 mins of arrival vs 86.1% by
anaesthetics.
However, anaesthetics only become inv...
It is interesting to once again read an article comparing the abilities of
anaesthetic vs. emergency department staff to perform RSI.
Unfortunately, I feel this article has been tarnished by two areas of
bias.
The first area is considered under 'time to RSI'. The emergency physicians
intubated 94% of patients within 15 mins of arrival vs 86.1% by
anaesthetics.
However, anaesthetics only become involved once they are contacted by the
emergency department. We are not psychic and therefore are instantly at a
disadvantage time wise in getting to the patient. If the emergency
physicians delay in contacting us in any way this would have been
reflected in the time to RSI.
The second comparative figure was that of physiological compromise. Once
again the anaesthetic department must be requested to attend any sick
patient. If the emergency physician decides to intervene on sicker
patients we have no control over this. More bias to the results.
Most studies to date have suffered from similar selection bias. Until a
proper randomised controlled trial is carried out there must be real
caution in making such comparisons between anaesthetic and emergency
department RSI.
Management of RSI is not just about times and percentages.
Anaesthetists often approach a sick patient in a different way.
A patient with reduced saturations initially requires good oxygen
therapy eg. high flow via non rebreath mask. The hypotensive patient often
requires good fluid resuscitation, whilst the patient with a reduced GCS
needs good prevention of hypoxia and hypoperfusion, which does not
immediately mean intubation.
A poorly prepared and performed RSI can result in hypotension,
hypertension, hypoxia and death. Once the airway is secured it requires
the ability to keep that patient intubated with sedation, paralysis,
appropriate ventilation and their subsequent transfer to definitive care.
I think as a whole anaesthetists tend to think about the consequences
of their interventions and prepare more before they carry out an RSI.
The multi speciality approach to the sick patient is probably the
best providing each group works together rather than competitively. Other
than an obstructed airway there are few situations where RSI is needed
immediateley.
If it can truely be shown to be in the patient's best interest for
emergency physicians to manage the airway then there is no problem. If
not, lets try not to chip away at each other's speciality skills.
Can people doubt that doing a task daily is far better than
occasionally?
I've visited this issue before (ref 1) and still remain to be convinced that long-chain superglues are less 'toxic' than short-chain DIY superglues, given that no superglue should ever be placed in a wound. The exothermic and the cyanate components of the argument are also completely overstated; millions get superglue on their fingers everyday and dont feel the heat or keel over with cyanide toxicity!
I'm afraid...
Dear Editor
“Trials are nothing like real life” is a complaint that defines a common problem in the practice of evidence-based medicine. Differences between patient populations or the circumstances of trials and real life often leave us bewildered when trying to determine the applicability of clinical research to the care of our own patients. Sometimes inclusion and exclusion criteria for subjects in trials mean t...
Sir-
I presume that Dr Fairhurst is referring to a substance used ubiquitously in the Antipodes and more commonly spelled 'methoxyflurANE'.
It is estimated that over three million doses have been used over the last 25 years in Australia (Jacobs, 2010). It is used by state ambulance services in the pre-hospital environment in most states of Australia, by the Australian Defence Forces, within emergency de...
Dear Sir,
We read with interest the article by Chen et al which demonstrated that a MEDS score greater than 12 may be discriminant for Emergency Department (ED) triage, ICU placement (1). These results of importance are in accordance with those of our group. We prospectively evaluated the accuracy of the MEDS score in 286 patients with documented sepsis admitted into our medical ICU (10 beds) after an ED cons...
I read the study with interest but felt that there was no way of knowing what type of patient cases the productivity was being based on. By this I mean that it is very possible that the SHOs and FY2s saw different cases mixes, ie one saw more simple minor injuries than the other. Also I could not see a mention as to the varying experiences of the FY2s and SHOs, were the SHOs all first year SHOs and had some of them no...
Are 'operative findings' a gold standard for diagnosis of a septic joint? Discussion of interpretation of synovial fluid in Roberts: Clinical Procedures in Emergency Medicine, 4th ed, suggests that gout, pseudogout and other arthritides can give turbid fluid. This clearly has a major impact on interpretation of the data.
I found this article which showed suboptimal use of chaperones in emergency departments to be of great interest. In my clinical work in primary care in the UK, I often struggle with providing a chaperone for intimate examinations. The two main issues I have are who we should bring in, and what should they see.
Firstly I feel that the person brought in should be someone who is allowed to examine patients themsel...
Dear Editor:
ASSESSMENT SCORE OR NOT!!
The LOW COST RES-Q-SCOPE(R) where digital video technology makes life a little easier. The patented and FDA Registered RES-Q-SCOPE(R)is readily available and considered essential in the emergency field, where the emergency needs to be dealt with quickly and effectively. The situations commonly found more frecuently by Paramedics, Medics in the military, First respo...
Dear Editor,
Indeed we are indebted to Dr. Ayrik for his comments on one of the most dramatic cardiovascular emergencies: aortic dissection. He rightly points out, that acute aortic dissection may not always present with the classical cardinal symptoms, particularly the sudden, sharp and tearing pain. Moreover, the author states that 10 % of aortic dissections are painless and he warns that the diagnosis ca...
Dear Editor
It is interesting to once again read an article comparing the abilities of anaesthetic vs. emergency department staff to perform RSI. Unfortunately, I feel this article has been tarnished by two areas of bias.
The first area is considered under 'time to RSI'. The emergency physicians intubated 94% of patients within 15 mins of arrival vs 86.1% by anaesthetics. However, anaesthetics only become inv...
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