Abstract

In recent years, the incidence of craniocerebral trauma has increased, making it one of the important causes of death and disability in neurosurgery patients. The decompressive craniectomy (DC) after severe craniocerebral injury has become the preferred treatment for patients with severe craniocerebral injury, but the incidence of postoperative hydrocephalus has become a difficult problem in clinical treatment. This study observed the changes of nerve growth factor (NGF), adrenocorticotropic hormone (ACTH), and arginine vasopressin (AVP) levels in the CSF after DC in patients with craniocerebral injury and analyzed the relationship between the three indicators and communicating hydrocephalus. The results showed that the levels of NGF, ACTH, and AVP in patients with cranial injury after DC were significantly higher than those in healthy subjects, and subdural effusion, traumatic subarachnoid hemorrhage (tSAH), and the levels of NGF, ACTH, and AVP in the CSF were independent risk factors for communicating hydrocephalus. Monitoring the levels of NGF, ACTH, and AVP is of great significance for clinicians to judge the occurrence of traffic hydrocephalus, evaluate the prognosis of patients with craniocerebral injury after DC, and guide clinical treatment.

Highlights

  • Craniocerebral injury is the most common cause of death and disability in surgical patients [1]

  • nerve growth factor (NGF) was determined by Enzyme-Linked ImmunoSorbent Assay (ELISA), and the kit was purchased from Shanghai Waran Biotechnology Co., LTD

  • Single-Factor Analysis of Influencing Communicating Hydrocephalus after decompressive craniectomy (DC) of Craniocerebral Injury. ere were no significant differences in age, gender, type of craniocerebral injury, Glasgow Coma Scale (GCS), and Galveston Orientation and Amnesia Test (GOTA) score between patients with and without communicating hydrocephalus (P > 0.05)

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Summary

Introduction

Craniocerebral injury is the most common cause of death and disability in surgical patients [1]. DC is an effective surgical procedure for reducing intracranial pressure [2]. With the promotion of this surgical procedure, the mortality of patients with severe craniocerebral injury has decreased [3]. Communicating hydrocephalus is one of the postoperative complications of DC induced by CSF malabsorption caused by the increase of CSF protein and the inflammatory viscosity of arachnoid particles [4]. Some studies have confirmed that DC is one of the risk factors for communicating hydrocephalus, but the mechanism is still unclear [5]. It is important to clarify the potential molecular mechanism and risk factors for communicating hydrocephalus after DC for head injury and to improve patient outcomes

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