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January 2008 - Volume 6 Issue 1
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From the Editor
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Original Contributon and Clinical Investigation

Determinants of satisfaction with primary health care settings and services among patients visiting primary health care centres in Qateef, Eastern Saudi Arabia
Ghazi M Al Qatari, M. Comm. H., Dave Haran

Factors predicting immunization coverage in Tikrit city
Mahmudul Hasan
........................................................

Medicine and Society

Scorpion Stings in Jordanian Children
Eman A Rawabdeh, Hussein A Bataineh
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Education and Training
Henoch-Schonlein Purpura: Presentation Patterns in Arab children in Kuwait
Mohammed M. Tohmaz, Samir I Saleh, Fahed AL-Anezi
Henoch-Schönlein Purpura in Jordanian Children
Maher khader, Wajdi Ammayreh, Ahmed Issa, Salah Abdallat, Basem Momani
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Clinical Research and Methods
Reproductive/sexual health knowledge, opinions and attidudes of university students
Ayfer Gemalmaz , Serpil Aydin , Nazli Sensoy
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Clinical Report
Rupture of Non Communicating Rudimentary Uterine Horn Pregnancy
Hansa Dhar
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Office Based Family Medicine
Urgent Neuroimaging in children with first nonfebrile seizures
Hussein I Alawneh, Hussein A Bataineh
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Monthly Surgery Tips
Hernias
Dr Maurice Brygel

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February 2008 - Volume 6, Issue 1

Scorpion Stings In Jordanian Children
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Eman A Rawabdeh, Hussein A Bataineh

From Department of Pediatrics and pharmacy at Prince Rashed Hospital (PRH) 2001-2005.
Pediatrician email: Bataineh_Hussein@yahoo.com.
P.O. Box 260 Aidoun, 21166, Irbid, Jordan.

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ABSTRACT

Objective: To determine which scorpion stings need treatment with antivenom.

Material: This review study was based on analysing cases of scorpion stings in children seen during 2001 to 2005 at (PRH) which is a referral hospital in north of Jordan.

Results: In our series of 386 cases, 201 (52%) were asymptomatic and 185 (48%) were showing some local or general symptoms of envenomation at the time of arrival to the hospital emergency department. Of these 185 symptomatic cases, 169 had developed symptoms within two hours of the sting and all 185 by four hours.

Conclusion: Completely asymptomatic cases which remain so during observation need not be given antiscorpion serum, which should be avoided if possible.

Keywords: scorpion, antivenom.
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.

INTRODUCTION

Scorpion envenomation is common in tropical and subtropical regions, especially in North Africa, Latin America, India, and the Middle East, where it is seen as a public-health problem.1, 2

The current therapeutic strategies rely partly on supportive symptomatic treatments.2 Scorpion antivenom is, however, the only specific treatment and is widely used in many countries such as Brazil and Saudi Arabia.2, 3-5
So the suggested treatment regimes are:
1) no antivenom serum, 6symptomatic treatment only;
2) 1 mL antivenom intramuscularly;7 and
3) 5 mL intravenous antivenom in all cases.

MATERIALS AND METHODS

This study was based on scorpion sting cases in children seen during 2001 to 2005 in Prince Rashed hospital which is a referral hospital in north of Jordan. The total number of cases seen was 386, with ages varying from one year to 12 years, the youngest of which was a baby of 10 months. The patients comprised 237 males and 149 females. Fifty-three of them were below two years, 125 were between two to five years, and 208 were between five and 12 years of age.

Management Protocol
The treatment of scorpion envenomation consists of nonspecific or supportive care and specific treatment with scorpion antivenom, which should be species-specific. We gave 5 mL antivenom intravenously in all cases.

Patients with a history of reactions to antivenom were excluded. We gave 10 mL antivenom in moderate systemic affection and 15-20 mL in severely affected cases showing signs of myocarditis or central nervous system (CNS) affection. The antivenom used was purified polyvalent anti-scorpion serum produced by the Egyptian Organisation for Biological Vaccine Production in Cairo, Egypt. The serum was prepared from the purified plasma of healthy horses immunized with venoms of Leiurus quinquestriatus, and Androctonus amoreuxi, and capable of neutralizing venoms of L. quinquestriatus, A. amorexi, A. crassicauda, and A. Aeneas and Buthus occitanus.

Non-specific (supportive) treatment consisted mainly of chlorpromazine (largactil) 0.5 to 2 mg/kg, repeated once or twice, and sometimes promethazine (phenergan) 0.25 to 1mg/kg was adequate to control autonomic symptoms and agitation.

For convulsions, diazepam 0.1 to 0.5 mg/kg was used, and occasionally had to be repeated. For cardiac complications like pulmonary edema, myocarditis and heart failure, frusemide 1 to 3 mg/kg, and ACE inhibitors like captopril were used.

For cerebral edema, appropriate therapy, such as mannitol, dexamethazone, hyperventilation, etc., were used. Cases which showed marked respiratory distress or impending respiratory failure were put on mechanical ventilation.

RESULTS

In our series of 386 cases, 201 (52%) were asymptomatic and 185 (48%) were showing some local or general symptoms of envenomation at the time of arrival at the hospital. Of these 185 symptomatic cases, 169 had developed symptoms within two hours of the sting and all 185 by four hours.
Twenty-nine (7.5%) had local symptoms like pain, swelling, redness, and itching lasting for between two and four hours. Systemic involvement was seen in 156 cases (40%). General symptoms such as salivation, sweating, extreme irritability, agitation and excessive crying were present in 132 cases (32%). Priapism was present in 52 affected male children (22%). The symptom wise presentation, laboratory and radiological abnormalities are listed in Table 1.

Cardiovascular and neurological complications cause the most morbidity and are major causes of mortality in scorpion envenomation. Neurological complications were the next most common feature, and were seen in 51 cases (13%). The main neurological complications were extreme agitation and disorientation, muscular spasms, seizures, coma and cerebral edema, which is the most dreaded complication. A girl of four years who presented to hospital in a comatose condition after about six hours of envenomation died of cerebral edema.

A total of 182 patients (163 symptomatic and 19 asymptomatic) were given 5 mL antivenom intravenously. Reactions were seen in 25 patients (13.7%), with minor transient skin reactions in 23 (12.6%) of them. In two patients (1%), the reactions were more serious, such as severe urticaria, periorbital edema, cough, breathlessness, severe hypotension and heart failure. One symptomatic patient who was given serum intravenously started showing signs of anaphylactoid reaction within minutes, and had to be sent to ICU, where the patient eventually recovered.

None of the asymptomatic cases developed any symptoms during the 24 hours of observation. In the 163 symptomatic cases, antiscorpion venom serum was given. In the remaining 22 cases, it could not be given because of non-availability or hypersensitivity to serum. Those affected children who were given serum had fewer complications, and shorter hospital stay, and there were no deaths in the group.

The hospital stay in the group that was given serum was between 3 to 7. For those who were not given serum, it was between 7 to 13 days.

DISCUSSION

In humans, the effects of scorpion venom are due to stimulation of the hypothalmus, leading to hypothalamic discharges, and causing profound effect on sympathetic and parasympathetic systems.2

There is a massive release of catecholamines, probably causing shunting of blood from metabolically active areas. There may be a direct toxic effect of the venom on regional oxygen transport at the cellular level. There is persistent arterial and gastric mucosal acidosis and increased lactate concentration.8

A number of clinical cardiovascular syndromes and central nervous system dysfunctions may be seen as a result of the effects of the released transmitters. Myocarditis, heart failure, pulmonary edema, hypertension, acute myocardial infarction-like picture, rhythm disturbances, etc., may occur: Soomro et al.9 reported major cardiovascular complications, such as changes in blood pressure, reversible ECG abnormalities simulating myocardial ischemia or infarction, reversible echocardiographic changes of systolic dysfunction, congestive heart failure and pulmonary edema in 18.5% of cases of scorpion envenomation. Also in our series, cardiac complications such as pulmonary edema, myocarditis, changes in heart rate and rhythm, and cardiac failure were seen in 70 cases (18%). In one case of a 12-year-old boy, the electrocardiographic changes were striking.

The first ECG taken on admission showed ventricular bigeminy or coupling, but after 48 hours the ECG showed a picture of anterolateral wall infarction and ischemia, with Q-waves, raised ST and inverted T-waves in leads I and avL and tall T-waves in leads II, III, V3-V6. The ECG changes started regressing rapidly and after four days were showing normal ST-T-waves in LI and avL, the only remaining defect being Q-waves in lead I. After four weeks, the ECG had become completely normal. For cardiac complications, afterload reduction with either nifedipine or an angiotensin-converting enzyme inhibitor should be considered.

Central nervous system disturbances such as confusion, agitation, seizures, cerebral edema and coma are more common in children.10-12 All cases of scorpion sting should be kept under close observation for at least 12 hours.

Santhanakrishnan and Balagopal Raju13 reported a mortality rate of 2.7% for cases of all ages. In our series, there were two deaths in 1991, the first, a girl of one year who died of disseminated intravascular coagulopathy and renal failure, and the second, a girl of four years who died of cerebral edema. The mortality percentage in our series was 0.5%. In cases of definite envenomation, the earliest use of species-specific antivenom serum reduces mortality and morbidity. Still, it should always be borne in mind that antivenoms are animal-derived Igs. Because they are concentrates of animal serum, both immediate and delayed hypertension-sensitivity reactions are common, and may themselves be life-threatening.

Bond14 reported that 58% of patients treated with antivenom had a delayed onset of rash or symptoms of serum sickness, and states that the use of antivenom for the less severe envenomation may subject them to unjustified risk.

In our series, of the 182 patients who were given antivenom serum, minor reactions were seen in 13.7% and more serious reactions in 1%. With regards to treatment of completely symptomatic cases, which in our series were 201, of which 182 (90%) could not be given any serum; these patients did not develop any symptoms and were discharged home in good condition after 24 hours of observation.

From the review of our cases, it seems that completely symptomatic cases which remain so during observation need not be given antiscorpion serum, for, however small the risk may be, there is a substantial danger of serious reactions to the animal protein in the antivenom serum, and it should be avoided if possible.

Table 1. Correlation between type of seizure and abnormal neuroimaging. (n=386).
Symptoms and laboratory abnormalities
Number (%)

Local symptoms                 29 (7.5)

Generalized symptoms             156 (40)

Sweating, salivation          132 (34)

Vomiting, diarrhea                     86 (22)

Abdominal rigidity              30 (8)

Tachycardia                             125 (32)

Bradycardia                         3 (0.77)

Hypotension                                 7 (2)

Circulatory failure                 4 (1)

Breathlessness                            18 (5)

Pulmonary edema                 5 (1)

Respiratory failure                         1 (0.2)

Seizures                             17 (44)

Coma                                           7 (1.8)

Pupillary changes                19 (5)

Hemiplegia                                   1 (0.25)

Cerebral edema                    1 (0.25)

Priapism                                     52 (22)

Hyperglycemia                   22 (5.6)

Cardiac enzymes                         24 (6)

ECG changes                     30 (7)

Echo changes                               5 (1.2)

pulmonary edema                 5 (1.2)

Hyperkalemia                             20 (5)

Leukocytosis                      60 (16)

Asymptomatic                         201 (52)

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REFERENCES

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  2. Ismail M. The scorpion envenoming syndrome. Toxicon 1995; 33:825-8.
  3. Rezende NA, Amaral CSF, Freire-Maia L.Immunotherapy for scorpion envenomation in Brazil.Toxicon 1998; 36:1507-13.
  4. E l-Amine EO, Sultan OM, Almagamci MS, Elidressy A.Serotherapy in the management of sting in children in Saudi Arabia.Ann Trop Pediatr 1994; 14:21-24.
  5. Ismail M .the treatment of the scorpion envenomation syndrome: the Saudi experience with serotherapy.Toxicon 1994; 32:1019-26.
  6. Neal JR. Scorpion sting syndrome in Eastern Riyadh. Ann Saudi Med 1990; 10:383-8.
  7. Mahaba HM, El-Sayed S. Scorpion sting: is it a health problem in Saudi Arabia? Evaluation of management of cases. Saudi Med J 1996; 17:315- 21.
  8. Sofer S, Cohen R, Shapir Y, Chen L, Colon A, Scharf SM. Scorpion venom leads to gastrointestinal ischemia. Crit Care Med 1997; 25:834- 40.
  9. Soomro RM, Andy JJ, Kontractor S, et al. Cardiovascular complications of scorpion stings and the effects of antivenom. J Saudi Heart Assoc1998; 10:2-10.
  10. Moss J, Kezic T, Henry DP, Kopin IJ. Scorpion venom-induced discharge of catecholamines accompanied by hypertension. Brain Res 1973; 54:381-5.
  11. Karnad DR, Hemodynamic patterns in patients with scorpion envenomation. Heart 1998; 79:485-9.
  12. Gueron M, Ilia R, Sofer S. The cardiovascular system after scorpion envenomation: a review. J Toxicol Clin Toxicol 1992; 30:245-58.
  13. Santhanakrishnan BR, Balagopal Raju V. Management of scorpion sting in children. J Trop Med Hyg 1974; 77:133-5.
  14. Bond GR. Antivenom administration for centruroides scorpion sting: risks and benefits. Ann Emerg Med 1992; 21:788-91.
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