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This research aimed to investigate the clinical efficacy of aerosol inhalation of ambroxol hydrochloride combined with terbutaline on children with severe pneumonia, and to evaluate its influence on their immune function and inflammatory level.

Totally 113 severe pneumonia children were included. Thereinto, 55 children in the control group (CG) were treated with terbutaline aerosol inhalation, while 58 in the research group (RG) were given ambroxol hydrochloride on the basis of the CG. Their symptom alleviating time, blood gas parameters, adverse reactions during treatment, clinical efficacy, immune function and inflammatory factors were compared.

The time of fever clearance time, disappearance of cough and pulmonary rates, chest shadow absorption and hospitalization of children in the RG were shorter than those in the CG. The combined treatment did not increase additional adverse reactions; instead, its effective rate was markedly higher than that in the CG. U0126 inhibitor Further research found that after treatment, the arterial partial pressure of oxygen (PaO

), oxygenation index (OI), CD4+ and CD4+/CD8+, and interleukin-10 (IL-10) levels were dramatically increased, while the arterial partial pressure of carbon dioxide (PaCO

), C-reactive protein (CRP), interleukin-6 (IL-6), interleukin-17 (IL-17) and CD8+ levels were obviously increased. In addition, these indexes of children in the RG were obviously better than those in the CG.

Aerosol inhalation of ambroxol hydrochloride combined with terbutaline has a remarkable clinical efficacy on children with severe pneumonia, which can improve their immune function and reduce inflammatory reaction.

Aerosol inhalation of ambroxol hydrochloride combined with terbutaline has a remarkable clinical efficacy on children with severe pneumonia, which can improve their immune function and reduce inflammatory reaction.

To evaluate the application value of responsibility-based nursing intervention in the nursing of patients with both diabetes mellitus (DM) and pulmonary tuberculosis (PTB).

A total of 180 patients with both DM and PTB admitted to our hospital from April 2019 to April 2020 were enrolled as research objects, of which 86 patients were under routine nursing intervention as a regular group (Reg group) and other 94 patients were under responsibility-based nursing intervention as a responsibility group (Res group). The unhealthy emotion, treatment compliance, self-efficacy, self-care ability, and life quality of both groups were evaluated after nursing intervention, and they were compared in blood glucose level and PTB treatment outcome.

After intervention, the Res group got lower self-rating anxiety scale (SAS) and self-rating depression scale (SDS) scores than the Reg group (both

<0.05). The Res group also got higher scores of self-efficacy, self-care ability, and life quality, and showed significantly higher treatment compliance rate and nursing satisfaction than the Reg group after intervention (all

<0.05). Additionally, after intervention, the Res group got higher scores of life quality than the Reg group (all

<0.05). The levels of fasting blood glucose (FBG), 2 hour postprandial blood glucose (2h PG), and glycosylated hemoglobin (HbA1c) in the Res group were lower than those in the Reg group, and the cavity closure rate, sputum negative conversion rate, and focus absorption rate of the Res group were all significantly higher than those of the Reg group (all P<0.05).

Responsibility-based nursing intervention can improve the treatment compliance, self-management ability, self-efficacy, and life quality of patients with both DM and PTB.

Responsibility-based nursing intervention can improve the treatment compliance, self-management ability, self-efficacy, and life quality of patients with both DM and PTB.

To explore the effects of comfort care on the recovery quality of oral and maxillofacial surgery patients undergoing general anesthesia.

Ninety-eight oral and maxillofacial surgery patients undergoing general anesthesia were recruited for this prospective study and were then randomly divided into two groups. The patients in the experimental group (49 cases) underwent comfort care, and the patients in the control group (49 cases) underwent routine care. Several indexes, including the hemodynamic indexes, the analgesic dosages, the recovery times, the extubation complications, the recovery room indwelling times, the related complications, and the final satisfaction scores were recorded and compared between the two groups.

Compared with the control group, the analgesic dosages and the recovery times in the experimental group were largely decreased (P<0.05), the occurrences of cough reactions during extubation were strongly reduced (P<0.05), and the recovery room indwelling times were also effectively shortened (P<0.05). In addition, the patients' hemodynamics in the experimental group were more stable during the recovery period (P<0.05), and the other complications, except for incision dehiscence, were significantly reduced (P<0.05), and the patient satisfaction scores were also much higher in the experimental group than they were in the control group (P<0.05).

The recovery times of oral and maxillofacial surgery patients undergoing general anesthesia were largely shortened, and the complications during the recovery period were effectively reduced with the help of the comfort care, so it is worthy of further research and clinical promotion.

The recovery times of oral and maxillofacial surgery patients undergoing general anesthesia were largely shortened, and the complications during the recovery period were effectively reduced with the help of the comfort care, so it is worthy of further research and clinical promotion.

To observe the efficacy of intrauterine Bakri balloon tamponade (IBBT) combined with ascending uterine artery ligation (AUAL) in the treatment of postpartum hemorrhage (PPH) due to uterine inertia after cesarean section.

A total of 92 patients with PPH due to uterine inertia after cesarean section were divided into a study group (n=46) and a control group (n=46) in accordance with the random number table. The control group was treated with IBBT alone, while the study group was treated with IBBT combined with AUAL. The clinical efficacies, hemorrhage, surgical duration, hospital stay, hemorrhage rate after removal of tamponade, recurrence rate of PPH, changes in coagulation function and quality of life were compared between the two groups.

The overall response rate (ORR) in the study group was 95.65%, remarkably higher than that of 80.43% in the control group (

< 0.05). The study group had a lesser amount of hemorrhage at 2 h and 24 h after surgery, a longer surgical duration, a shorter hospital stay, and lower hemorrhage rate after removal of tamponade and recurrence rate of PPH than the control group (

< 0.