Correspondence
Anaesthesia, 2003, 58, pages 597–616
....................................................................................................................................................................................................................
.
The ‘wall effect’ is usually manifested
oxygenation during one-lung anaes-
thesia is related to the response to
compression of the non-dependent
There was no skin rash evident. She had
obvious macroglossia, with bloodstained
secretions on her pillow, and she was
by PaO2 values displayed on the
CIABG monitor that gradually decrease
with time but which are not accom-
lung. British Journal of Anaesthesia 2003; stridulous. On air, her SpO remained
2
panied by changes in either PaCO or
90: 21–6.
pH values [1]. Although the phenom- 5 Ishikawa S, Ohmi S, Nakazawa K,
above 92%, with a pulse rate of
2
)
1
70 beat.min , and BP 108 ⁄ 55 mmHg.
There was no bronchospasm on auscul-
tation, and no evidence of heart failure.
In view of her airway compromise and
enon was rarely seen in our total clinical
experience of over 200 cases, the ‘wall
effect’ is considered to be one of the
major causes of inaccurate CIABG data.
In our previous research, specifically
involving a total of 28 oesophagec-
tomy patients [2–4] and 50 patients who
underwent thoracotomy [5], the ‘wall
effect’ was never observed.
Makita K. Continuous intra-arterial
blood gas monitoring during thoracic
surgery. Journal of Anesthesia (Official
Journal of the Japan Society of Anesthesi- fluctuating GCS, the patient was trans-
ology) 2000; 14: 119–23.
ferred to the ICU, where an anaesthetic
machine was available for inhalational
induction of anaesthesia.
Once on the ICU, further intraven-
ous access was secured, together with
invasive arterial BP monitoring. During
this period, nebulised epinephrine
(5 ml, 1 : 1000) was administered, with
immediate improvement in her airway.
The degree of macroglossia improved
enough to allow speech. Humidified O2
was continued, and hydrocortisone and
antihistamines, both type 1 (H1) and
type 2 (H2), given. She was not intu-
bated, and remained stable over the
next 8 h with adequate arterial oxygen
saturations, and arterial blood gas ana-
lysis showing normal acid-base balance
with good gas exchange. She was
discharged to a medical ward with no
further compromise. Her macroglossia
gradually settled.
Potassium permanganate is regularly
used in the management of suppurative
eczema, and ulcers, and has previously
been used as an abortifacient. Ingestion
of dilute solutions can cause brown
staining of the mouth and throat, sore
throat, abdominal pains, vomiting and
dysphagia. Concentrated solutions, or
dry crystals as in this case, can cause
swelling and bleeding of lips and
tongue, pharyngeal oedema and swell-
ing of the larynx, as well as gastrointes-
tinal burns. Systemic effects do not
usually manifest, due to poor absorb-
ance, but can include tachycardia,
hypotension, hallucinations, methaem-
aglobinaemia and cyanosis, metabolic
acidosis, haemolysis, pancreatitis and
coma [2, 3]. Some effects can
be delayed up to 36 h postingestion
including disseminated intravascular
coagulation (DIC), cardiac failure and
hepato-renal failure. In 1996, Young
et al. postulated that the damage from
Airway obstruction following
potassium permanganate
ingestion
Since the PaCO and the pH data
2
were unaffected in this case, we assumed
that the ‘wall effect’ occurred when the
first arterial blood sample was drawn for
calibration. The subsequent linear in-
Potassium permanganate (KMnO ) is a
4
highly corrosive, water-soluble oxid-
izing antiseptic for cleansing and
deodorizing suppurative eczematous
reactions and wounds, used in baths
and wet bandages. It is presented as a
crease in PaO on the CIABG monitor
2
might be explained by the reversal of the
‘
wall effect’, although it would be very
difficult to prove this hypothesis. As far as
we know, a spontaneous reversal of the
0
.1% solution, diluted 10 times to yield
a 0.01% solution, or crystals that are
dissolved, and applied until the skin
becomes dry [1]. Both the crystals and
concentrated solutions are caustic to
skin, eyes, upper respiratory tract and
mucous membranes, resulting in coagu-
lation necrosis.
An 81-year-old woman was admitted
to Accident and Emergency following
deliberate ingestion of an unknown
‘
wall effect’ has not been previously
reported. This case suggests that a ‘wall
effect’ reversal can occur spontaneously
and that it may cause the CIABG mon-
itor to overestimate PaO values, espe-
2
cially when the CIABG data has
been calibrated to an arterial blood gas
analyser.
S. Ishikawa
K. Nakazawa
amount of KMnO crystals, which were
4
K. Makita
being regularly applied to suppurative
chronic leg ulcers. She had a history of
heart failure, chronic renal failure and
atrial fibrillation, for which she was
receiving warfarin. She had refused oral
fluid replacement on admission and
Tokyo Medical and Dental University,
Tokyo 113–8519, Japan
E-mail: ishikawa.mane@tmd.ac.jp
References
1
2
3
Mahutte CK, Sassoon CSH, Muro JR, intravenous replacement was started.
et al. Progress in the development of a She remained cardiovascularly stable
fluorescent intravascular blood gas sys-
without respiratory compromise and
tem in man. Journal of Clinical Monitoring her SpO remaining above 92% on air.
2
1
990; 6: 147–57.
She was also commenced on intraven-
ous antibiotics for presumed incidental
cutaneous infection.
Twelve hours after admission, I was
asked to review the patient on the ward,
because she had a reduced level of
Ishikawa S, Makita K, Nakazawa K,
Amaha K. Continuous intra-arterial
blood gas monitoring during
oesophagectomy. Canadian Journal of
Anaesthesia 1998; 45: 273–6.
Ishikawa S. Oxygenation may improve consciousness and was snoring. The
with time during one-lung ventilation. nursing staff also noticed that her tongue
Anesthesia and Analgesia 1999; 89:
58–9.
had swollen in the preceding hour. On
initial assessment, she was rousable with
a Glasgow coma scale (GCS) of 11. She
was afebrile, pale, with cool peripheries.
2
4
Ishikawa S, Nakazawa K, Makita K.
Progressive changes in arterial
ingestion of KMnO crystals was due to
4
6
06
ꢀ 2003 Blackwell Publishing Ltd