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. Author manuscript; available in PMC: 2011 Jul 28.
Published in final edited form as: Hum Exp Toxicol. 2008 Jun;27(6):513–518. doi: 10.1177/0960327108091861

Table 1.

Summary of baseline characteristics of all patients in the cohort

Ad hoc dose
N=119
Titrated dose
N=153
P Value
Males 85 (71%) 90 (59%) 0.031*
Age (years)¥ 25 (20-35) 26 (22-38) 0.025*
Anti-cholinesterase pesticide
OPs
 Chlorpyrifos 93 (78%) 56 (37%) <0.0001*
 Dimethioate 3 (3%) 28 (18%) <0.0001*
 Other Ops£ 18 (15%) 38 (25%) 0.04*
Carbamate 5 (4%) 13 (8%) N/S
 unknown anti-cholinesterase pesticide 0 (0%) 18 (12%) <0.0001*
Amount poison ingestion (ml.)¥ 27 (10-80) 50 (25-100) 0.002*
Post ingestion time on admission (hrs)¥ 4 (2-9) 4 (3-7) N/S
Direct admission 89 (75%) 24 (16%) <0.0001*
Atropine given before admission 20 (17%) 66 (43%) <0.0001*
Alcohol ingestion 34 (29%) 29 (19%) N/S
GCS <15 71 (60%) 110 (72%) <0.033*
GCS 9-14 35 (29%) 20 (13%) <0.0009*
GCS ≤ 9 36 (30%) 90 (59%) <0.002*
Co-morbid illness 15 (13%) 22 (14%) N/S
Pulmonary signs (crepitations) 25 (21%) 55 (36%) 0.007*
Ventilated at baseline 1 (1%) 9 (6%) 0.002*
Pralidoxime administered 48 (40%) 32 (21%) 0.0005*

Data are number (%) unless otherwise indicated.

¥

Median (IQR).

Others: Diazinon, Phenthoate, Acephate, Profenofos, Fenthion, unknown Ops

£

Co-morbid illness included cardiac, pulmonary, psychiatric, neurologic and undiagnosed disorders

*

Results that are significantly different and corresponding P value