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青霉素和天然免疫可预防脾切除术后败血症。

Penicillin and natural immunity protect against postsplenectomy sepsis.

作者信息

Livingston C D, Levine B A, Sirinek K R

出版信息

J Surg Res. 1983 Apr;34(4):332-6. doi: 10.1016/0022-4804(83)90080-x.

DOI:10.1016/0022-4804(83)90080-x
PMID:6834816
Abstract

Prophylactic penicillin, splenic autotransplantation, and immunization using pneumococcal vaccine have all been shown to reduce the incidence and mortality of postsplenectomy sepsis. However, little is known regarding the effect of penicillin in established infection or the effect of prior infection in either asplenic controls or animals with autotransplanted splenic tissue. An animal model with bacterial introduction via the lungs was used to investigate the effect of penicillin, splenic autotransplantation, and previous exposure to the infecting organism on the mortality of postsplenectomy sepsis. One hundred fifty-nine rats underwent either sham celiotomy, intraperitoneal splenic autotransplantation, or splenectomy. Twelve weeks postoperatively all animals were challenged using Streptococcus pneumoniae delivered transtracheally. Half of each group received procaine penicillin by intramuscular injection for 5 days beginning 24 hr post bacterial inoculation and mortality was observed. Eight weeks later surviving rats that had received penicillin were reinoculated with the same organism and mortality was again observed. Splenic autotransplantation reduced the early mortality in postsplenectomy sepsis. Prior bacterial exposure reduced the mortality in postsplenectomy sepsis, even in splenectomized animals. Treatment with penicillin produced a marked reduction in mortality even when administration was postponed for 24 hr after bacterial inoculation.

摘要

预防性使用青霉素、脾自体移植以及接种肺炎球菌疫苗均已被证明可降低脾切除术后败血症的发病率和死亡率。然而,关于青霉素在已确诊感染中的作用,以及既往感染在无脾对照动物或脾组织自体移植动物中的影响,人们了解甚少。采用经肺部引入细菌的动物模型,来研究青霉素、脾自体移植以及既往接触感染病原体对脾切除术后败血症死亡率的影响。159只大鼠分别接受假剖腹术、腹腔内脾自体移植或脾切除术。术后12周,所有动物经气管内注入肺炎链球菌进行攻击。每组动物的一半在细菌接种后24小时开始,通过肌肉注射给予普鲁卡因青霉素,持续5天,并观察死亡率。8周后,对之前接受过青霉素治疗的存活大鼠再次接种相同病原体,并再次观察死亡率。脾自体移植降低了脾切除术后败血症的早期死亡率。即使是在脾切除的动物中,既往接触细菌也降低了脾切除术后败血症的死亡率。即使在细菌接种后24小时才开始使用青霉素治疗,也能显著降低死亡率。

相似文献

1
Penicillin and natural immunity protect against postsplenectomy sepsis.青霉素和天然免疫可预防脾切除术后败血症。
J Surg Res. 1983 Apr;34(4):332-6. doi: 10.1016/0022-4804(83)90080-x.
2
Protection from postsplenectomy sepsis: Effect of prophylactic penicillin and pneumococcal vaccine on clearance of type 3 Pneumococcus.脾切除术后败血症的预防:预防性青霉素和肺炎球菌疫苗对3型肺炎球菌清除的影响。
Surgery. 1983 Jun;93(6):792-7.
3
Improved survival rate for intraperitoneal autotransplantation of the spleen following pneumococcal pneumonia.肺炎球菌肺炎后脾脏腹腔内自体移植的存活率提高。
Surg Gynecol Obstet. 1983 Jun;156(6):761-6.
4
Site of splenic autotransplantation affects protection from sepsis.脾自体移植部位影响对脓毒症的保护作用。
Am J Surg. 1983 Dec;146(6):734-7. doi: 10.1016/0002-9610(83)90329-x.
5
Protection against pneumococcal sepsis in splenectomized rats by implantation of splenic tissue into an omental pouch.通过将脾组织植入网膜囊对脾切除大鼠进行肺炎球菌败血症的防护。
Surgery. 1982 Jun;91(6):638-41.
6
The efficacy of postsplenectomy sepsis prophylactic measures: the role of penicillin.
J Trauma. 1988 Aug;28(8):1285-8. doi: 10.1097/00005373-198808000-00027.
7
The effects of experimental splenic autotransplantation and imipenem-cilastatin treatment in postsplenectomy Pseudomonas aeruginosa sepsis.实验性脾自体移植和亚胺培南-西司他丁治疗对脾切除术后铜绿假单胞菌败血症的影响。
Res Exp Med (Berl). 1995;195(3):163-9. doi: 10.1007/BF02576785.
8
Optimal site and amount of splenic tissue for autotransplantation.自体移植的脾脏组织的最佳部位和数量。
J Surg Res. 1992 Aug;53(2):109-16. doi: 10.1016/0022-4804(92)90021-q.
9
Comparison of omental splenic autotransplant to partial splenectomy. Protective effect against septic death.大网膜脾自体移植与部分脾切除术的比较。对感染性死亡的保护作用。
Am Surg. 1987 Dec;53(12):702-5.
10
Splenic autotransplantation provides protection against fatal sepsis in young but not in old rats.脾自体移植可保护幼鼠免受致命性败血症的侵害,但对老年大鼠则无此作用。
J Pediatr Surg. 1992 Sep;27(9):1207-12. doi: 10.1016/0022-3468(92)90789-a.

引用本文的文献

1
A four-year experience with splenectomy versus splenorrhaphy.脾切除术与脾修补术的四年经验
Ann Surg. 1985 May;201(5):568-75. doi: 10.1097/00000658-198505000-00005.