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Control of the External Hemorrhage (A) by Aluminum Chloride (50%) (B) and Suturing Technique (C) 

Control of the External Hemorrhage (A) by Aluminum Chloride (50%) (B) and Suturing Technique (C) 

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Despite all the progress in surgical science, bleeding caused by traffic accidents is still one of the challenges surgeons face in saving patients' lives. Therefore, introducing an effective method to control external bleeding is an important research priority. This study aimed to compare the hemostatic effect of aluminum chloride versus simple sut...

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... with blood proteins, and this property makes alu- minum chloride a very efficient hemostatic agent. Then, it may be an effective hemostatic agent that adequately satisfies surgeons’ need to control bleeding even in pa- tients with abnormal body hemostatic system. Although the hemostatic effect of aluminum chloride has already been found, its effect in controlling external bleeding has not assessed and compared with suturing technique as a standard method. This study aimed to compare the hemostatic effect of aluminum chloride versus simple suturing technique in controlling external hemorrhage. This experimental study took place at Kashan University of Medical Sciences from August 2013 to December 2013. In this study, 60 male Wistar rats (weighting 180 - 230 g) were randomly allocated into 6 groups (simple random- ization) of 10 rats each. According to the pilot study, mean hemostatic time of the six groups were 43.3, 30.6, 19.6, 15.3, 9.1, 84.3 seconds, respectively and total variance was 16.9. Considering α = 0.05 and 1-β = 0.8, sample size was estimated at 10 in each group. One week before study, ani- mals were kept at 21 ± 1°C with a 12-hour light/dark cycle (lights on from 8:00 AM to 8:00 PM). They had free access to standard rat chaw and water ad libitum. Rats were anesthetized by intraperitoneal (ip) injection of a ketamine/xylazine mixture (ketamine 100 mg/kg and xylazine 10 mg/kg). The 10% ketamine and 2% xylazine (Alfasan, Holland) were purchased from local supplier (Shahid-Beheshti Hospital Pharmacy, Kashan, Iran). An incision of two cm in length and half a cm in depth was made on each rat’s shaved back skin by scalpels NO. 10. Aluminum chloride was purchased from Merck, (Darm- stadt, Germany). Aqueous solution of aluminum chlo- ride was prepared in five concentrations of 50%, 25%, 15%, 10% and 5% (w/v) in distilled water, each concentration to be used in one group of rats. Half a milliliter volume of solution was applied to the incision site by an insulin syringe. The times of hemostasis were measured using a chronometer. The hemostasis time was considered as the time required for complete drying of bleeding and no blood discharge from the incision site (Figure 1). The mean of the measured times in the ten rats in each group was considered as the hemostatic time for each alumi- num chloride concentration. Simple suturing using ny- lon 3-0 was used as the standard method of hemostasis in the control group. All simple sutures were performed by one surgeon. After controlling external bleeding, each rat was treated intraperitoneally with 50 mg keflin (1 g cefalotin/10 mL, Aspen Pharmacare Australia Pty Ltd, Aus- tralia). Seven days after the treatment, all rats were anesthe- tized using IP injections of a mixture of ketamine and xylazine (ketamine 100 mg/kg and xylazine 10 mg/kg). Then, the rats were placed in a prone posture on the op- erating table and the previous sites of treatment were resected. The resected tissues were immediately fixed in formalin and were sent for the pathology report. Based on the defined pathological grading (6-8), the pathology results were classified into 6 groups including: Zero: no change, 1: minor inflammatory infiltration without ede- ma, 2: mild to moderate inflammatory infiltration with mild edema, 3: mild to moderate inflammatory infiltra- tion and moderate edema, 4: moderate inflammation with neutrophils scattered and diffuse edema, 5: severe inflammation of the tissue and edematous changes, fi- brosis and hemorrhage. Animal handling and all experiments were performed in accordance with the international guidelines set out in the Guide for the Care and Use of Laboratory Animals (Institute of Laboratory Animal Resources, 1996) and ap- proved by the local research council at Kashan University of Medical Sciences, Kashan, Iran. (grant number:9378, ethical code:1912) Data analysis was performed using SPSS software ver- sion 16 (SPSS, Inc., Chicago, IL, USA). Kolmogorov-Smirnov test was used to determine if the data are normally dis- tributed and this was not the case. To compare the mean hemostatic time in the aluminum chloride groups, the Kruskal-Wallis test was used. Moreover, the Mann-Whit- ney U test was used to compare the mean hemostasis times in the aluminum chloride groups and that of the control group (suturing technique). The mean hemostatic time in the groups aluminum chloride concentrations of 50% (Group 5), 25% (Group 4), 15% (Group 3), 10% (Group 2) and 5% (Group 1) were 8.20 ± 0.919, 14.10 ± 1.37, 21.20 ± 1.31, 30.80 ± 1.68 and 42.00 ± 4.19 seconds, respectively. Also, the mean hemostatic time in the control group (Group 6) was 84.00 ± 4.05 seconds (mean ± standard deviation). A significant difference was observed between the hemostatic time in different concentrations of aluminum chloride (Group 1 and 2, P value = 0.003), (Group 2 and 3, P value = 0.001), (Group 3 and 4, P value = 0.004), (Group 4 and 5, P value = 0.005). Moreover, a significant difference was observed between the hemostatic time in the groups with different concen- trations of aluminum chloride and the control group, so that the hemostatic time in all the experimental groups were significantly less than that of the control group (P value = 0.002) (Table 1). The pathology examination showed that all the wounds were in grade 1 on the third day after the experiment ex- cept the wounds in the groups in which 25% and 50% con- centrations of aluminum chloride were utilized (Table 2). No wound was in grades 0, 3, 4 and 5. Acidic property of aluminum chloride can be seen in Figure 1. This acidic property after reaction with blood proteins creates a bar- rier by coagulated proteins, and prevents the outflow ...
Context 2
... with blood proteins, and this property makes alu- minum chloride a very efficient hemostatic agent. Then, it may be an effective hemostatic agent that adequately satisfies surgeons’ need to control bleeding even in pa- tients with abnormal body hemostatic system. Although the hemostatic effect of aluminum chloride has already been found, its effect in controlling external bleeding has not assessed and compared with suturing technique as a standard method. This study aimed to compare the hemostatic effect of aluminum chloride versus simple suturing technique in controlling external hemorrhage. This experimental study took place at Kashan University of Medical Sciences from August 2013 to December 2013. In this study, 60 male Wistar rats (weighting 180 - 230 g) were randomly allocated into 6 groups (simple random- ization) of 10 rats each. According to the pilot study, mean hemostatic time of the six groups were 43.3, 30.6, 19.6, 15.3, 9.1, 84.3 seconds, respectively and total variance was 16.9. Considering α = 0.05 and 1-β = 0.8, sample size was estimated at 10 in each group. One week before study, ani- mals were kept at 21 ± 1°C with a 12-hour light/dark cycle (lights on from 8:00 AM to 8:00 PM). They had free access to standard rat chaw and water ad libitum. Rats were anesthetized by intraperitoneal (ip) injection of a ketamine/xylazine mixture (ketamine 100 mg/kg and xylazine 10 mg/kg). The 10% ketamine and 2% xylazine (Alfasan, Holland) were purchased from local supplier (Shahid-Beheshti Hospital Pharmacy, Kashan, Iran). An incision of two cm in length and half a cm in depth was made on each rat’s shaved back skin by scalpels NO. 10. Aluminum chloride was purchased from Merck, (Darm- stadt, Germany). Aqueous solution of aluminum chlo- ride was prepared in five concentrations of 50%, 25%, 15%, 10% and 5% (w/v) in distilled water, each concentration to be used in one group of rats. Half a milliliter volume of solution was applied to the incision site by an insulin syringe. The times of hemostasis were measured using a chronometer. The hemostasis time was considered as the time required for complete drying of bleeding and no blood discharge from the incision site (Figure 1). The mean of the measured times in the ten rats in each group was considered as the hemostatic time for each alumi- num chloride concentration. Simple suturing using ny- lon 3-0 was used as the standard method of hemostasis in the control group. All simple sutures were performed by one surgeon. After controlling external bleeding, each rat was treated intraperitoneally with 50 mg keflin (1 g cefalotin/10 mL, Aspen Pharmacare Australia Pty Ltd, Aus- tralia). Seven days after the treatment, all rats were anesthe- tized using IP injections of a mixture of ketamine and xylazine (ketamine 100 mg/kg and xylazine 10 mg/kg). Then, the rats were placed in a prone posture on the op- erating table and the previous sites of treatment were resected. The resected tissues were immediately fixed in formalin and were sent for the pathology report. Based on the defined pathological grading (6-8), the pathology results were classified into 6 groups including: Zero: no change, 1: minor inflammatory infiltration without ede- ma, 2: mild to moderate inflammatory infiltration with mild edema, 3: mild to moderate inflammatory infiltra- tion and moderate edema, 4: moderate inflammation with neutrophils scattered and diffuse edema, 5: severe inflammation of the tissue and edematous changes, fi- brosis and hemorrhage. Animal handling and all experiments were performed in accordance with the international guidelines set out in the Guide for the Care and Use of Laboratory Animals (Institute of Laboratory Animal Resources, 1996) and ap- proved by the local research council at Kashan University of Medical Sciences, Kashan, Iran. (grant number:9378, ethical code:1912) Data analysis was performed using SPSS software ver- sion 16 (SPSS, Inc., Chicago, IL, USA). Kolmogorov-Smirnov test was used to determine if the data are normally dis- tributed and this was not the case. To compare the mean hemostatic time in the aluminum chloride groups, the Kruskal-Wallis test was used. Moreover, the Mann-Whit- ney U test was used to compare the mean hemostasis times in the aluminum chloride groups and that of the control group (suturing technique). The mean hemostatic time in the groups aluminum chloride concentrations of 50% (Group 5), 25% (Group 4), 15% (Group 3), 10% (Group 2) and 5% (Group 1) were 8.20 ± 0.919, 14.10 ± 1.37, 21.20 ± 1.31, 30.80 ± 1.68 and 42.00 ± 4.19 seconds, respectively. Also, the mean hemostatic time in the control group (Group 6) was 84.00 ± 4.05 seconds (mean ± standard deviation). A significant difference was observed between the hemostatic time in different concentrations of aluminum chloride (Group 1 and 2, P value = 0.003), (Group 2 and 3, P value = 0.001), (Group 3 and 4, P value = 0.004), (Group 4 and 5, P value = 0.005). Moreover, a significant difference was observed between the hemostatic time in the groups with different concen- trations of aluminum chloride and the control group, so that the hemostatic time in all the experimental groups were significantly less than that of the control group (P value = 0.002) (Table 1). The pathology examination showed that all the wounds were in grade 1 on the third day after the experiment ex- cept the wounds in the groups in which 25% and 50% con- centrations of aluminum chloride were utilized (Table 2). No wound was in grades 0, 3, 4 and 5. Acidic property of aluminum chloride can be seen in Figure 1. This acidic property after reaction with blood proteins creates a bar- rier by coagulated proteins, and prevents the outflow ...

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... epinephrine) and alpha-adrenergic (0.05% tetra hydrazine HCl, 0.05% oxymetazoline HCl, 0.025% phenyl epinephrine HCl). Astringents include chlorides of aluminium (10, 20, 25% AlCl₃) and iron (8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19)(20) and sulphates of aluminium [20-25% Al₂(SO₄)₃] and iron (15.5, 20, and 12.7 Fe(SO)₄). All the currently known astringents cause some local temporary tissue damage, and vasoconstrictors elicit negative systemic effects. ...
... These characteristics make it a suitable hemostatic agent due to the blood's high protein content. 60 Aluminum chloride acts by creating a barrier formed by the coagulated blood proteins that prevent blood flow from the arteries, thus preventing its possible systemic side effects. This mechanism may provide sufficient hemostasis, even in patients with bleeding disorders. ...
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... 5 Aluminum chloride hexahydrate solution at varying concentrations demonstrated a significant reduction in hemostasis time compared to the control group. 7 However, there is limited research directly comparing the time to hemostasis among these three chemical cautery solutions. ...
... The chemical cautery solutions investigated in this study have all been validated as an effective means of achieving hemostasis. [5][6][7][8][9] However, there are risks and benefits to each of these cautery solutions that should assist in clinical decisions. ...
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