開(kāi)放性胸部創(chuàng)傷胸腔封閉器材的研制和胸部外固定新型器材的研制及應(yīng)用
[Abstract]:background
The incidence of thoracic traumaTT (IR) in all previous wars (IR) is about 8%, and the direct cause of death accounts for 25% of the death of the trauma. It is the second cause of death in the type of trauma only next to the craniocerebral injury. Open chest trauma is the main injury caused by the death in the chest trauma, and the open chest trauma caused by the explosion injury during the war. More common, open chest trauma accounts for 7% to 12% of the total number of wounded. In the naval battle, the incidence is up to 20%., if it can be treated at the front, it will create an opportunity for follow-up treatment and greatly reduce the death rate of open chest trauma (MR). The most important first aid method of open chest trauma is the early side rescue. It is important to restore the integrity of the chest wall and the negative pressure in the chest as soon as possible to prevent severe respiratory dysfunction. How to close the thoracic cavity in time and effectively is the key. Open chest trauma combined with rib fracture and even flail chest (flail chest FC), the patient often causes severe chest pain and breathing difficulties during the closed chest delivery. It is difficult to restrain the respiratory movement of the patients and to choose the proper material to fix the chest wall, which can effectively relieve the pain of the chest wall and prevent the collapse of the chest wall as an integral part of the treatment of chest trauma. Equipment and other first-aid equipment, the simple gauze dressings used in first aid have various shortcomings, which can not meet the needs of ETOB and pre-HC, and have developed and equipped simple emergency equipment to simplify operation, implement timely, correct front line treatment and pre hospital first aid, and reduce the mortality rate (MR). Important practical significance.
Part I: Design and fabrication of a temporary thoracic sealing device with one-way valve disc and animal experimental study
Objective: to design and prepare one way valve petal temporary pleural sealing device, and to evaluate the closed effect in the first aid of open chest trauma through the open chest trauma field first aid animal experiment.
Methods: dogs were used as experimental animals. The animals were randomly divided into control group (4 rats) and experimental group (4 rats) to establish an open thoracic injury animal model. The control group was closed by the common clinical application, and the experimental group was closed by the one way valve temporary pleural sealing device. The closed thoracic operation time of the 2 groups of dogs was observed and the thoracic closed drainage was performed. Operating time, heart rate, respiratory rate, oxygen saturation, maximal pulling force and drainage effect of thoracic cavity sealing device were studied.
Results: the experimental group was (0.58 + 0.14) min, and the control group was (1.17 + 0.21) min. The two groups had statistical significance (P0.01), the former was superior to the latter; the operation time of the closed thoracic drainage in the experimental group was (0.48 + 0.07) min, the control group was (2.20 + 0.11) min, and the two groups were statistically significant (P0.01), the former was superior to the latter. In the experimental group, the changes of heart rate (HR), respiratory frequency (RR) and oxygen saturation (SpO2) before and after thoracic closure were statistically significant (P 0.05). There was no significant difference between the two groups after drainage at each time point in the pleural effusion (P0.05).
Conclusion: the one way valve petal temporary pleural sealing device can effectively close the thoracic cavity in time, and the open chest trauma is closed thoracic trauma. The fixation effect is accurate, then it can be used for the effective thoracic closed drainage and the following treatment. It is suitable for the frontline treatment and pre hospital emergency treatment for open chest trauma patients.
Part 2: Design, fabrication and clinical trial of pneumatic pressure-adjustable external fixation chest band
Objective: To design and prepare a pneumatic pressure-regulated external fixation chest band, and to evaluate its effect on chest trauma fixation, pain relief and breathing improvement through clinical controlled trials.
Methods: 50 patients in our department were randomly divided into experimental group and control group by digital table method, with 25 cases in each group. The experimental group used air column pressure regulating external fixed chest band to fix the chest, and the control group used the common elastic chest band. The pain score (VAS) and the respiratory frequency (RR) were observed in the two groups of patients at all time points at all time points. A portable pulmonary function tester was used to test the pulmonary function of two groups of patients before and after operation 24h, 48h, 72h. Blood gas analysis was performed before and after operation, 24h, 48h, 72h. The first active cough time of two groups of patients after operation, the total amount of thoracic injection, the extraction time of thoracic duct, the number of hospitalization days after operation, the incidence of pulmonary complications (IR) and the total dosage of analgesics were recorded.
Results: the pain scores and respiratory frequency differences of 3H, 6h, 24h, 48h and 72h were statistically significant (P 0.05) in the experimental group and the control group (P 0.05). The pain scores and respiratory frequency differences were statistically significant (P 0.05) in the experimental group and the control group after the operation of 3H, 6h, 24h, 48h, and 72h (P 0.05). FEV1% estimated value, the difference between the MVV% predicted value and the control group was statistically significant (P 0.05), the difference between the experimental group FEV1/FVC and the control group was not statistically significant (P0.05). The difference between the experimental group PaO2, PaCO2, SpO2 and the control group was not statistically significant (P0.05). In the experimental group, the first active cough time after the operation, the dosage of postoperative analgesic drugs and the control group were in the experimental group. The difference was statistically significant (P 0.05). There was no significant difference between the total amount of thoracic fluid intake in the experimental group, the time of drainage tube extraction, the number of days after the operation and the incidence of pulmonary complications compared with the control group (P0.05).
Conclusion: the external fixation of air column pressure external fixation has a beautiful appearance, the material is safe and soft, the patient has strong comfort after wearing, and its fixation effect is accurate. It can improve the pain threshold of the patient, reduce the pain of the patient, promote the patient's active cough and expectoration, and be beneficial to the recovery of lung function. It should be used for emergency treatment of chest trauma patients and postoperative chest surgery. The patient's chest is fixed.
Combined with the results of the above experimental results, this study shows that the one way valve petal temporary pleural sealing device can effectively close the thoracic cavity in time, change the open chest trauma to closed thoracic trauma, and be suitable for the frontline and pre hospital emergency treatment of open thoracic trauma. The recovery of lung function is suitable for front-line treatment of chest trauma, pre-hospital first aid and chest fixation of patients after clinical thoracic surgery.
【學(xué)位授予單位】:第二軍醫(yī)大學(xué)
【學(xué)位級(jí)別】:碩士
【學(xué)位授予年份】:2014
【分類號(hào)】:R655
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