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2018 101
ABSTRACT
KEYWORDS Aluminum phosphide (ALP) poisoning has aroused interest in the past three
Aluminium phosphide, decades. The percentage of poisoning is low, but the mortality is high and no
Suicide, effective antidote available. The objective of this study was to find out predictors of
Mortality, mortality for patients with acute aluminium phosphide poisoning. All patients with
Shock, acute aluminium phosphide poisoning admitted to Poisoning Control Center, Ain
Acidosis, Shams University Hospital between the years 2015 to 2017 were prospectively
Arrhythmia studied and compared between survival and non survivor patients. Data collected
include demographic data, clinical manifestations, laboratory parameters, ECG and
treatment offered to the patients. A total 31 patients were enrolled comprising 20
males and 11 females, 84% were suicide and mortality rate was 35%. Shock and
cardiac arrhythmia were observed in 52% and39% respectively, while 26%
presented with coma. Abnormal blood sugar and metabolic acidosis were found in
19% and 45% respectively. Fifty two percent of the patients needed inotropic
therapy and 32% received N-acetylcysteine (NAC). Risk factors increasing mortality
were found as shock, tachycardia, coma, metabolic acidosis, hyperglycemia, cardiac
arrhythmia and the need for inotropic drug therapy. The study concluded that
aluminum phosphide is a low-cost highly-toxic rodenticide. The circulatory collapse,
metabolic acidosis and cardiac arrhythmia are the major causes of death. The role of
NAC must be reassessed in larger scale. So, intensive observation in ICU and
aggressive symptomatic management should be urgently taken into consideration.
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to hospital and there is significant difference the first day. So, if patients pass the first day,
between both groups as regards period of stay there is a good chance to survive (Table 1).
at hospital and patients who died usually die in
Table (1): Statistical analysis of the gender, mode of poisoning, period of stay, age and delay time
of presentation to hospital for both studied groups.
Non survivor Survivor
Total
Parameters group group Statistic test p
n = 31
n = 11 n= 20
Gender
Males 7 13 20 (65%)
X2ChS= 0.006 0.9
Females 4 7 11 (35%)
Mode of poisoning
Suicidal 11 15 26 (84%)
X2ChS = 3.3 0.07
Accidental 0 5 5 (16%)
Period of stay at hospital
<1 day 11 11 22 (71%)
X2ChS = 6.9 0.008*
>1 day 0 9 9 (29%)
Age
Age (years)
25 ± 11 23±14 24 ± 13 t = 0.4 0.7
Mean ±SD
Delay time of presentation to hospital
Delay Time
(hours) 4±2 5±2 4.5 ± 2 t = 1.1 0.3
Mean ±SD
n: number, SD: standard deviation, * significant
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Table (2): Statistical analysis of the clinical parameters for both studied groups.
Non
Survivor
survivor Total Chi-square
Parameters group p
group n = 31 test (χ2)
n =20
n= 11
Heart rate (HR)
Abnormal 9 3
Not palpable (4) (1)
12 (39%)
Tachycardia (3) (1) 13.4 0.0002*
Bradycardia (2) (1)
Normal 2 17 19 (61%)
Blood pressure (BP)
Shock 11 5 16 (52%)
15.9 0.0006*
Normal 0 15 15 (48%)
Conscious level
Coma 6 2 8 (26%)
7.4 0.006*
Normal 5 18 23 (74%)
Vomiting
Yes 7 8 15 (48%)
1.6 0.2
No 4 12 16 (52%)
n: number, * significant
statistical analysis revealed significant
The laboratory analysis of studied
difference between both groups as regards
patients revealed, 19% of the studied patients
blood sugar and acid base status and no
had abnormal blood sugar, 45% had metabolic
significant difference as regards liver and renal
acidosis, 10% had abnormal liver function test
function tests (Table 3).
and no patients had renal abnormalities. The
Table (3): Statistical analysis of the laboratory analysis for both studied groups.
Non survivor Survivor
Total Chi-square
Parameters group group p
n= 31 test (χ2)
n= 11 n =20
Random blood glucose level
Abnormal
a) Hyperglycemia 5 0
6 (19%)
b) Hypoglycemia 1 0 13.5 0.0002*
Normal 5 20 25 (81%)
Acid – base status
Metabolic acidosis 10 4 14 (45%)
14.4 0.0001*
Normal 1 16 17 (55%)
Abnormal liver function tests
Yes 1 2 3 (10%)
0.007 0.9
No 10 18 28 (90%)
Abnormal renal function tests
Yes 0 0 0 (0%)
0 1
No 11 20 31(100%)
n: number, * significant
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Table (4): Statistical analysis of the ECG abnormalities for both studied groups
Non survivor Survivor
Total Chi-square
Parameters group group p
n= 31 test (χ2)
n= 11 n =20
Cardiac Arrhythmia
Total number 7 5
VT (2) (0)
Bradycardia (2) (1)
12 (39%)
PVC (1) (1) 4.5 0.03*
AF (1) (0)
Ischemic changes (1) (2)
Nodal rhythm (0) (1)
Normal 4 15 19 (61%)
n: number, * significant
groups as regard the usage of inotropes and
The inotropic therapy was given in 52%
NAC (Table 5).
of the patients and in 32% NAC was given and
there is significant difference between both
Table (5): Statistical analysis of the given therapy for both studied groups.
Non survivor Survivor
Total Chi-square test
Parameters group group p
n= 31 (χ2)
n= 11 n =20
Inotropic therapy
Yes 11 5 16 (52%)
15.9 0.00006*
No 0 15 15 (48%)
NAC therapy
Yes 6 4 10 (32%)
3.9 0.05*
No 5 16 21 (68%)
n: number, * significant
The mortality of the moderate to severe receive NAC and no significant difference
patients who received NAC was 60% versus between both groups as regard the mortality
83% in those moderate to severe who did not (Table 6).
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Table (6): Statistical comparison of mortality in patients who received NAC and patients did not
receive NAC in the moderate to severe patients
NAC therapy No NAC therapy
Chi-square test (x) p
n =10 n= 6
Survivor group 4 (40%) 1 (17%)
Non survivor group 6 (60%) 5 (83%) 0.95 0.3
Total 10 6
n: number.
A logistic regression analysis of the metabolic acidosis, cardiac arrhythmia and
significant parameters revealed that the usage of inotropic therapy are predictors of
tachycardia, shock, coma, hyperglycemia, mortality (Table 7).
Table (7): Logistic regression analysis of the significant parameters to detect predictors associated
with aluminium phosphide poisoning-related mortality.
Non survivor Survivor group
Parameters OR (95%CI) p
group n= 11 n =20
Heart rate (HR)
Abnormal 9 3 26
0.001*
Normal 2 17 4 to 182
Blood pressure (BP)
Shock 11 5 65
0.006*
Normal 0 15 3 to 1294
Conscious level
Coma 6 2 11
0.01*
Normal 5 18 2 to 71
Random blood glucose level (mg/dl)
Abnormal 6 0 49
0.01*
Normal 5 20 2 to 999
Acid – base status
Metabolic
10 4 40
acidosis 0.002*
4 to 411
Normal 1 16
ECG results
Cardiac
7 5 5
arrhythmia 0.04*
1 to 26
Normal 4 15
Inotropic therapy
Yes 11 5 65
0.006*
No 0 15 3 to 1294
n: number, * significant, OR = odds ratio, CI = confidence interval.
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cardiovascular collapse, 37% had coma and guidelines but due to unavailability of the drug
46% had vomiting. Also, Erfantalab et al. only 10 patients received NAC so we cannot use
(2017) demonstrated that blood pressure and their results in the prediction of outcome. At the
pulse rate were significantly different between same time we got benefit from this limitation in
ALP survivors and non-survivors groups. comparing between patients who received NAC
and patients who did not received NAC in the 16
As regard laboratory analysis the results
moderate to severe cases. As showing the
revealed that 19% had abnormal blood sugar,
mortality rate in the patients who received NAC
45% had metabolic acidosis, 10% had
was 60% (6 died out of 10 patients) while
abnormal liver function tests and no one had
mortality in the group did not receive NAC was
renal abnormalities. The statistical analysis
83% (5 died out of 6 patients) and the statistical
revealed significant difference between both
analysis revealed no significant difference
groups as regard blood sugar and acid base
between both groups.
status. Similar results were obtained by Sulaj
et al. (2015) who found that among 140 Similar results obtained by Karanth and
patients whom died out of 317 in his study of Nayyar (2003) where they found that treatment
ALP poisoning, 88% had metabolic acidosis with NAC in ALP poisoning had no therapeutic
and 16% had hyperglycemia. Also, Erfantalab advantage. In contrast, Bhat et al. (2015) found
et al. (2017) demonstrated that the blood pH, that among 26 patients treated with NAC out of
and serum bicarbonate level were 100 ALP poisoning patients, mortality in the
significantly different between survivors and treated patients was 2% versus 21.6% in non
non-survivors groups. treated patients and the difference was
statistically significant. Moreover, Tehrani et al.
The results revealed that 39% had ECG
(2013) found that NAC prolong survival time,
abnormalities; the statistical analysis revealed
stabilize blood pressure and pulse rate. Also,
that there was significant difference between
Agarwal et al. (2014) found that NAC lower
non survivor and survivor groups as regarded
mortality, hospitalization time, and the
ECG abnormalities. Also, Aziz and Husain,
frequency of intubation and mechanical
(2015) studied 80 patients with acute ALP
ventilation.
poisoning and found that 10 % developed
cardiac arrhythmia and the most frequent The logistic regression analysis revealed
arrhythmia was atrial fibrillation (31% of that tachycardia, shock, coma, hyperglycemia,
patients) followed by ventricular fibrillation metabolic acidosis, cardiac arrhythmia and the
(20%), ventricular tachycardia (17%) and AV need of inotropic therapy were predictors of
block (12%). Moreover, Sulaj et al. (2015) in mortality in acute ALP. Similar results were
their study of 317 ALP poisoned patients obtained by Mathai and Bhanu (2010) where
found that 44% had sinus tachycardia and they found that hypotension requiring vasoactive
11% had other cardiac rhythm disorders. drugs, low pH, coma and need for mechanical
ventilation were predictive of mortality from
The results revealed that 52% of the
acute ALP poisoning. While Sulaj et al. (2015)
patients need inotropic therapy and in 32%
found that the negative prognostic factors related
NAC was received and there were significant
to the fatalities were high dosage of the toxic
difference between both groups as regard
agent, the long delay (a mean of 4 hours); the
inotropic and NAC used. As regard NAC
lack of vomiting, and the depth of coma upon
there was limitation in our study where we
presentation.
had 16 patients graded moderate to severe and
must take NAC according to our local
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Tawfik 109
Conclusion References
Mansoura J. Forens. Med. Clin. Toxicol., Vol. 26, No. 2, July. 2018
Tawfik 110
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ﻣﺮﻛﺰ ﻋﻼج اﻟﺘﺴﻤﻢ ﻣﺴﺘﺸﻔﯿﺎت ﺟﺎﻣﻌﺔ ﻋﯿﻦ ﺷﻤﺲ
أﺛﺎر ﺗﺴﻤﻢ ﻓﻮﺳﻔﯿﺪ اﻷﻟﻮﻣﻨﯿﻮم اﻻھﺘﻤﺎم ﺑﺰﯾﺎدة ﻋﺪد اﻟﺤﺎﻻت ﻓ ﻲ اﻟﻌﻘ ﻮد اﻟﺜﻼﺛ ﺔ اﻟﻤﺎﺿ ﯿﺔ .ﻋﻠ ﻰ اﻟ ﺮﻏﻢ ﻣ ﻦ أن
اﻟﻨ ﺴﺒﺔ اﻟﻤﺌﻮﯾ ﺔ ﻟﻠﺘ ﺴﻤﻢ ﻣﻨﺨﻔ ﻀﺔ ،إﻻ أن ﻣﻌ ﺪل اﻟﻮﻓﯿ ﺎت ﻣﺮﺗﻔ ﻊ ﻟﻠﻐﺎﯾ ﺔ و ﻻ ﯾﻮﺟ ﺪ ﺗﺮﯾ ﺎق ﻓﻌ ﺎل ﻟﻌ ﻼج ﻣﺜ ﻞ ھ ﺬة
اﻟﺤﺎﻻت .ﻛﺎن اﻟﮭﺪف ﻣﻦ ھﺬه اﻟﺪراﺳﺔ ھ ﻮ اﻛﺘ ﺸﺎف ﺗﻨﺒ ﺆات ﻟﻠﻮﻓ ﺎة ﺑﺎﻟﻨ ﺴﺒﺔ ﻟﻠﻤﺮﺿ ﻰ اﻟ ﺬﯾﻦ ﺗﻌﺮﺿ ﻮا ﻟﻠﺘ ﺴﻤﻢ اﻟﺤ ﺎد
ﺑﻔﻮﺳﻔﯿﺪ اﻷﻟﻮﻣﻨﯿﻮم .درﺳﻨﺎ 31ﻣﺮﯾﻀﺎ ﯾﻌﺎﻧﻮن ﻣﻦ اﻟﺘ ﺴﻤﻢ اﻟﺤ ﺎد ﺑﻔﻮﺳ ﻔﯿﺪ اﻷﻟﻮﻣﻨﯿ ﻮم وﺗ ﻢ دﺧ ﻮﻟﮭﻢ ﻣﺮﻛ ﺰ ﻋ ﻼج
اﻟﺘ ﺴﻤﻢ ﻣﺴﺘ ﺸﻔﻰ ﺟﺎﻣﻌ ﺔ ﻋ ﯿﻦ ﺷ ﻤﺲ ﺑ ﯿﻦ ﻋ ﺎم ٢٠١٥إﻟ ﻰ ﻋ ﺎم ٢٠١٧وﺗﻤ ﺖ ﻣﻘﺎرﻧ ﺔ ﺑ ﯿﻦ اﻟﻤﺮﺿ ﻰ اﻟﻨ ﺎﺟﯿﻦ
واﻟﻤﺮﺿﻰ اﻟﻤﺘﻮﻓﯿﻦ .وﺗﺸﻤﻞ اﻟﺒﯿﺎﻧﺎت اﻟﺘﻲ ﺗﻢ ﺟﻤﻌﮭﺎ اﻟﺒﯿﺎﻧﺎت اﻟﺪﯾﻤﻮﻏﺮاﻓﯿ ﺔ ،واﻷﻋ ﺮاض واﻟﻌﻼﻣ ﺎت اﻟ ﺴﺮﯾﺮﯾﺔ ،
واﻟﻤﻌﺎﯾﯿﺮ اﻟﻤﺨﺘﺒﺮﯾ ﺔ ،و رﺳ ﻢ اﻟﻘﻠ ﺐ واﻟﻌ ﻼج اﻟﻤﻘ ﺪم ﻟﻠﻤﺮﺿ ﻰ .اﻟﻨﺘ ﺎﺋﺞ :ﺗ ﻢ ﺗ ﺴﺠﯿﻞ ٣١ﻣﺮﯾ ﻀﺎ وﻛ ﺎن ﻣ ﻨﮭﻢ ٢٠
ذﻛﺮا و ١١أﻧﺜﻰ ،وﻛﺎن ﻧﺴﺒﺔ اﻟﻤﻨﺘﺤ ﺮﯾﻦ .٪ ٨٤و ﻣﻌ ﺪل اﻟﻮﻓﯿ ﺎت .٪ ٣٥ﻟ ﻮﺣﻆ ھﺒ ﻮط ﺑ ﻀﻐﻂ اﻟ ﺪم وﺗﻐﯿ ﺮ ﻓ ﻰ
ﺿﺮﺑﺎت اﻟﻘﻠﺐ ﻓﻲ ٪ ٥٢و ٪ ٣٩ﻋﻠﻰ اﻟﺘﻮاﻟﻲ ،وﻛﺎن ٪ ٢٦أﺻﯿﺒﻮا ﺑﻐﯿﺒﻮﺑﺔ .و ﻟ ﻮﺣﻆ اﺧ ﺘﻼل ﻓ ﻰ ﻧ ﺴﺒﺔ اﻟ ﺴﻜﺮ
ﺑﺎﻟﺪم و زﯾﺎدة ﺣﻤﻮﺿﺔ اﻟﺪم ﻓﻲ ٪ ١٩و ٪ ٤٥ﻋﻠ ﻰ اﻟﺘ ﻮاﻟﻲ .ﻟ ﻮﺣﻆ اﺿ ﻄﺮاب ﻓ ﻰ ﺗﺨﻄ ﯿﻂ اﻟﻘﻠ ﺐ ﻓ ﻲ ٪ ٣٩ﻣ ﻦ
اﻟﻤﺮﺿﻰ.وﻛﺎن ٪ ٥٢ﻣﻦ اﻟﻤﺮﺿ ﻰ ﯾﺤﺘ ﺎﺟﻮن إﻟ ﻰ ﻋ ﻼج ﻟﺮﻓ ﻊ ﺿ ﻐﻂ اﻟ ﺪم وﺗﻠﻘ ﻰ ٪ ٣٢ان اﺳ ﺘﯿﻞ ﺳﯿ ﺴﺘﺎﯾﯿﻦ .
ووﺟﺪﻧﺎ اﻟﻌﻮاﻣﻞ اﻟﺘﺎﻟﯿﺔ ﺗﺰﯾﺪ ﻣﻦ ﺧﻄ ﺮ اﻟﻮﻓ ﺎة :ھﺒ ﻮط ﺿ ﻐﻂ اﻟ ﺪم ،ﻋ ﺪم اﻧﺘﻈ ﺎم ﺿ ﺮﺑﺎت اﻟﻘﻠ ﺐ ،ﺣ ﺪوث ﻏﯿﺒﻮﺑ ﺔ ،
زﯾﺎدة ﺣﻤﻮﺿﺔ اﻟﺪم ،ارﺗﻔﺎع ﻧﺴﺒﺔ اﻟﺴﻜﺮ ﻓﻲ اﻟﺪم ،اﺿﻄﺮاب ﺗﺨﻄﯿﻂ اﻟﻘﻠﺐ واﻟﺤﺎﺟﺔ إﻟﻰ ﻋ ﻼج ﻟﺮﻓ ﻊ ﺿ ﻐﻂ اﻟ ﺪم.
و ﻧﺨﻠﺺ إﻟﻰ أن ﻓﻮﺳﻔﯿﺪ اﻷﻟﻮﻣﻨﯿﻮم ھﻮ ﻣﺒﯿﺪ ﻋﺎﻟﻲ اﻟﺴﻤﯿﺔ ﻣﻨﺨﻔﻀﺔ اﻟﺘﻜﻠﻔ ﺔ ،وﯾﻌﺘﺒ ﺮ ھﺒ ﻮط اﻟ ﺪورة اﻟﺪﻣﻮﯾ ﺔ ،زﯾ ﺎدة
ﺣﻤﻮﺿﺔ اﻟﺪم وﻋﺪم اﻧﺘﻈﺎم ﺿﺮﺑﺎت اﻟﻘﻠ ﺐ ھ ﻲ اﻷﺳ ﺒﺎب اﻟﺮﺋﯿ ﺴﯿﺔ ﻟﻠﻮﻓ ﺎة .ﻟ ﻢ ﯾﻜ ﻦ ھﻨ ﺎك ﺗﺮﯾ ﺎق ﻓﻌ ﺎل ﻣﺘ ﺎح ﻟﻠﻌ ﻼج
وﯾﺤﺘﺎج ﺗﺮﯾﺎق ان اﺳﺘﯿﻞ ﺳﯿﺴﺘﺎﯾﯿﻦ اﻟﻰ إﻋﺎدة ﺗﻘﯿ ﯿﻢ ﻋﻠ ﻰ ﻧﻄ ﺎق اوﺳ ﻊ ،ﻟ ﺬا ﯾﺠ ﺐ أﺧ ﺬ اﻟﻤﻼﺣﻈ ﺔ اﻟﻤﻜﺜﻔ ﺔ ﻓ ﻲ وﺣ ﺪة
اﻟﻌﻨﺎﯾﺔ اﻟﻤﺮﻛﺰة واﻟﺘﺪﺧﻞ اﻟﻌﻼﺟﻰ اﻟﺴﺮﯾﻊ ﻻى أﻋﺮاض ﺗﻈﮭﺮ دون ﺗﻤﮭﻞ .
Mansoura J. Forens. Med. Clin. Toxicol., Vol. 26, No. 2, July. 2018