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1.
F1000Res ; 13: 548, 2024.
Article in English | MEDLINE | ID: mdl-39280770

ABSTRACT

Background: Head injuries are considered as a silent epidemic due to the high incidence rate throughout the world. The main cause of morbidity and mortality in patients with head injury is cerebral edema which is defined as abnormal fluid accumulation in the brain parenchyma. Mannitol is a hyperosmolar solution given to reduce fluid volume in the brain. Increased high intracranial pressure can affect prognosis and can be evaluated by assessing clinical outcomes in patients with severe traumatic brain injury using the Glasgow Outcome Discharge Scale (GODS) instrument. Methods: Observational analytical study with a cross sectional design on 50 patients with severe traumatic brain injury at dr. Zainoel Abidin General Hospital Banda Aceh to determine the effect of mannitol use on the clinical outcomes of severe traumatic brain injury patients which used t test analysis. Results: The mean value of the group that received mannitol had a higher GODS score than the group that did not receive mannitol. The results of the T test between groups obtained a p value of 0.000 which is smaller than 0.05, so it can be concluded that the use of mannitol has an effect on the GODS score in Severe traumatic brain injury patients. The results showed that the mean GODS value in patients who received mannitol was higher than those who did not receive mannitol. Conclusion: This concludes that the administration of mannitol is effective in improving the clinical outcomes of patients with severe traumatic brain injury at dr. Zainoel Abidin General Hospital Banda Aceh.


Subject(s)
Brain Injuries, Traumatic , Mannitol , Humans , Mannitol/therapeutic use , Brain Injuries, Traumatic/drug therapy , Male , Female , Adult , Middle Aged , Treatment Outcome , Cross-Sectional Studies , Glasgow Outcome Scale , Young Adult
2.
Medicina (Kaunas) ; 60(9)2024 Sep 20.
Article in English | MEDLINE | ID: mdl-39336578

ABSTRACT

Background and Objectives: This study aimed to develop an embolic agent with short-term embolic effects using cilastatin as the basic material. Materials and Methods: The particle size distribution of 25 mg cilastatin-based short-term embolic agents was evaluated microscopically under three different mixing conditions. A total of thirty-six healthy male Sprague Dawley rats were divided into four groups. Each group of six rats was injected once into the tail artery with 0.4 mL each of (A) Cilastatin + D-Mannitol Mixture, (B) Iohexol, (C) Prepenem, and (D) embolization promoter (EGgel). Results: A visual inspection of the tail appearance of rats in each group was performed at 0, 3, 7, 15, and 21 days. At weeks 1 and 3, three rats per group were euthanized, and histopathological analyses were performed on the specimens obtained from each group. No significant differences were observed on day 7, but mild inflammation was observed in Group (D) on day 15. Histopathological inflammation scoring of tail central artery embolization was performed using a six-point scale (from 0 = absent to 5 = marked inflammation). Three groups were formed consisting of six male New Zealand white rabbits each: control, positive control, and test groups. The control group received an Iohexol injection (rabbits: 0.8 mL). The positive control and experimental groups were injected with prepenem and cilastatin/D-mannitol compound, respectively (0.8 mL), and vascular angiography was performed. The order of occlusion progression after embolization was as follows: test group, positive control group, and control group. Conclusions: We developed a cilastatin/D-mannitol compound that exhibits characteristics of short-term embolization by utilizing the pharmacokinetic properties of cilastatin and the crystalline material D-mannitol. We evaluated its particle size distribution microscopically, conducted histopathological evaluation including inflammation via animal experiments, and assessed the embolization effect.


Subject(s)
Cilastatin , Protease Inhibitors , Animals , Male , Rabbits , Rats , Cilastatin/therapeutic use , Cilastatin/pharmacology , Embolism , Embolization, Therapeutic/methods , Iohexol , Mannitol/pharmacology , Mannitol/therapeutic use , Microvessels/drug effects , Particle Size , Rats, Sprague-Dawley , Protease Inhibitors/therapeutic use
3.
Open Heart ; 11(2)2024 Aug 22.
Article in English | MEDLINE | ID: mdl-39179251

ABSTRACT

OBJECTIVE: Postoperative delirium (POD), especially after cardiac surgery with cardiopulmonary bypass (CPB), is a relatively common and severe complication increasing side effects, length of hospital stay, mortality and healthcare resource costs. This study aimed to determine the impact of using mannitol serum in the prime of CPB for preventing the occurrence of delirium in patients undergoing coronary artery bypass surgery. METHODS: This study is a single-centre, double-blinded, randomised, controlled trial that was conducted from December 2022 to May 2023. Patients in the age range of 18-70 who underwent elective coronary artery bypass surgery were included in the study. In the control group (n=45), the prime solution included Ringer's lactate serum. In the intervention group (n=45), the prime solution consisted of 200 mL mannitol serum and Ringer's lactate serum. The primary outcome of the study was the incidence of POD. Secondary outcomes included the duration of mechanical ventilation, length of stay in the intensive care unit (ICU) and 30-day in-hospital mortality. RESULTS: There were no statistically significant differences in demographic characteristics and risk factors between the control and intervention groups (p<0.05). However, the incidence of POD was significantly lower in the intervention group compared with the control group (22.25% vs 42.2%, p=0.035). There were no significant differences between the two groups regarding CPB time, aortic cross-clamp time, duration of mechanical ventilation and length of stay in ICU (p<0.05). Additionally, mortality rates and rates of return to the operating room did not differ significantly between the two groups (p<0.05). CONCLUSIONS: This study concluded that adding mannitol to the prime of CPB pump can help reduce the incidence of delirium after cardiac surgery. TRIAL REGISTRATION NUMBER: IRCT20221129056660N1.


Subject(s)
Coronary Artery Bypass , Delirium , Mannitol , Postoperative Complications , Humans , Mannitol/administration & dosage , Mannitol/therapeutic use , Mannitol/adverse effects , Male , Female , Coronary Artery Bypass/adverse effects , Middle Aged , Double-Blind Method , Aged , Delirium/prevention & control , Delirium/epidemiology , Delirium/etiology , Incidence , Postoperative Complications/prevention & control , Postoperative Complications/epidemiology , Adult , Treatment Outcome , Risk Factors , Adolescent , Young Adult , Coronary Artery Disease/surgery , Hospital Mortality , Time Factors , Length of Stay , Follow-Up Studies
4.
Brain Inj ; 38(12): 977-984, 2024 Oct 14.
Article in English | MEDLINE | ID: mdl-38853675

ABSTRACT

OBJECTIVE: This study aimed to find out the efficacy of using Hypertonic saline solution (HSS) over mannitol in the management of TBI by comparing their performance in improving different outcomes. METHODS: Electronic databases were searched for randomized controlled trials (RCTs) assessing the impact of HSS vs. mannitol on ICP in patients who suffered TBI. Outcomes of interest were mortality, neurologic functional outcomes, risk ratio (RR) of successful ICP treatment, reduction in ICP after 30-60 and 90-120 min, improvement in cerebral perfusion pressure (CPP) at 30-60 and 90-120 min, and also treatment failure. Evaluations were reported as RR or mean difference (MD) with 95% confidence intervals (CIs) using weighted random-effects models. RESULTS: The analysis included 624 patients from 15 RCTs. HSS infusion had a significant impact on the improvement of CPP at 30-60 min [MD = 5.54, 95% CI (3.04, 8.03),p < 0.001] compared to mannitol. However, results yielded no significant difference between HSS and mannitol in terms of mortality, neurologic functional outcomes, successful ICP treatment, reduction in ICP after 30-60 min and 90-120 min, improvement in CPP at 90-120 min, and treatment failure. CONCLUSION: HSS and mannitol are both effective treatments for elevated ICP due to TBI. However, further research is required to derive a better comparison.


Subject(s)
Brain Injuries, Traumatic , Randomized Controlled Trials as Topic , Humans , Saline Solution, Hypertonic/therapeutic use , Saline Solution, Hypertonic/administration & dosage , Brain Injuries, Traumatic/drug therapy , Mannitol/therapeutic use , Mannitol/administration & dosage , Treatment Outcome , Diuretics, Osmotic/therapeutic use , Diuretics, Osmotic/administration & dosage , Intracranial Pressure/drug effects , Intracranial Pressure/physiology , Intracranial Hypertension/drug therapy , Intracranial Hypertension/etiology
5.
A A Pract ; 18(6): e01800, 2024 Jun 01.
Article in English | MEDLINE | ID: mdl-38864528

ABSTRACT

Central neurogenic hyperventilation (CNH) is a rare disease, caused by chemical or mechanical disturbance of respiratory centers. It is characterized by the absence of extracerebral respiratory stimuli. A woman developed severe respiratory alkalosis and lactatemia after resection of a posterior fossa meningioma despite lack of cardio-respiratory or metabolic alterations. Cerebral computed tomography (cCT) revealed edema of the pontomedullary area. Treatment with mannitol and dexamethasone reestablished normal breathing patterns. Lactatemia was likely due to reduced splanchnic lactate utilization. Intracranial pathologies should be suspected in case of hyperventilation without overt reasons. cCT to confirm edema or ischemia and prompt treatment is suggested.


Subject(s)
Alkalosis, Respiratory , Meningeal Neoplasms , Meningioma , Humans , Female , Meningioma/surgery , Meningioma/complications , Alkalosis, Respiratory/etiology , Meningeal Neoplasms/surgery , Meningeal Neoplasms/complications , Mannitol/therapeutic use , Mannitol/administration & dosage , Middle Aged , Dexamethasone/therapeutic use , Dexamethasone/administration & dosage , Hyperlactatemia/etiology , Infratentorial Neoplasms/surgery , Infratentorial Neoplasms/complications , Tomography, X-Ray Computed , Postoperative Complications/etiology
6.
Neurol Res ; 46(9): 883-892, 2024 Sep.
Article in English | MEDLINE | ID: mdl-38825027

ABSTRACT

OBJECTIVES: Controlling elevated intracranial pressure following brain injury with hyperosmolar agents is one of the mainstay treatments in traumatic brain injury patients. In this study, we compared the effects of hypertonic saline (HS) and mannitol in reducing increased intracranial pressure. METHODS: A total of 637 patients from 15 studies were included in our meta-analysis. The primary outcomes were mortality, the length of stay in the hospital and ICU, and the Glasgow Outcome Scale at follow-up. RESULTS: The mortality in the mannitol group was not statistically different compared to the HS group (RR = 1.55; 95% CI = [0.98, 2.47], p = 0.06). The length of stay in the ICU was significantly shorter in the HS group (MD = 1.18, 95% CI = [0.44, 1.92], p < 0.01). In terms of favorable neurological outcomes, there was no significant difference between the two agents (RR = 0.92, 95% CI = [0.11, 7.96], p = 0.94). The duration of the effect was shorter in the mannitol group than in the HS group (MD = -0.67, 95% CI = [-1.00, -0.33], p < 0.01). DISCUSSION: The results showed that HS and mannitol had similar effects in reducing ICP. Although the HS was associated with a longer duration of effect and shorter ICU stay, other secondary outcomes including mortality rate and favorable neurological outcomes were similar between the two drugs. In conclusion, considering the condition of each patient individually, HS could be a reasonable option than mannitol to reduce ICP in TBI patients.


Subject(s)
Brain Injuries, Traumatic , Intracranial Hypertension , Mannitol , Humans , Mannitol/therapeutic use , Brain Injuries, Traumatic/drug therapy , Brain Injuries, Traumatic/mortality , Brain Injuries, Traumatic/complications , Saline Solution, Hypertonic/therapeutic use , Intracranial Hypertension/drug therapy , Intracranial Hypertension/etiology , Length of Stay/statistics & numerical data
7.
Medicina (Kaunas) ; 60(6)2024 Jun 18.
Article in English | MEDLINE | ID: mdl-38929612

ABSTRACT

Background and Objectives: The relationship between histidine-tryptophan-ketoglutarate (HTK)-induced hyponatremia and brain injury in adult cardiac surgery patients is unclear. This study analyzed postoperative neurological outcomes after intraoperative HTK cardioplegia infusion. Materials and Methods: A prospective cohort study was conducted on 60 adult patients who underwent cardiac surgery with cardiopulmonary bypass. Of these patients, 13 and 47 received HTK infusion and conventional hyperkalemic cardioplegia, respectively. The patients' baseline characteristics, intraoperative data, brain injury markers, Mini-Mental State Examination (MMSE) scores, and quantitative electroencephalography (qEEG) data were collected. Electrolyte changes during cardiopulmonary bypass, the degree of hyponatremia, and any associated brain insults were evaluated. Results: The HTK group presented with acute hyponatremia during cardiopulmonary bypass, which was intraoperatively corrected through ultrafiltration and normal saline administration. Postoperative sodium levels were higher in the HTK group than in the conventional cardioplegia group. The change in neuron-specific enolase levels after cardiopulmonary bypass was significantly higher in the HTK group (p = 0.043). The changes showed no significant differences using case-control matching. qEEG analysis revealed a significant increase in relative delta power in the HTK group on postoperative day (POD) 7 (p = 0.018); however, no significant changes were noted on POD 60. The MMSE scores were not significantly different between the two groups on POD 7 and POD 60. Conclusions: HTK-induced acute hyponatremia and rapid correction with normal saline during adult cardiac surgeries were associated with a potential short-term but not long-term neurological impact. Further studies are required to determine the necessity of correction for HTK-induced hyponatremia.


Subject(s)
Cardiac Surgical Procedures , Heart Arrest, Induced , Hyponatremia , Mannitol , Procaine , Humans , Male , Hyponatremia/etiology , Female , Mannitol/administration & dosage , Mannitol/adverse effects , Mannitol/therapeutic use , Prospective Studies , Middle Aged , Procaine/adverse effects , Procaine/administration & dosage , Procaine/therapeutic use , Aged , Heart Arrest, Induced/methods , Heart Arrest, Induced/adverse effects , Cardiac Surgical Procedures/adverse effects , Cardiac Surgical Procedures/methods , Cardioplegic Solutions/administration & dosage , Cardioplegic Solutions/adverse effects , Cardioplegic Solutions/therapeutic use , Electroencephalography/methods , Glucose/administration & dosage , Glucose/therapeutic use , Adult , Cohort Studies , Cardiopulmonary Bypass/methods , Cardiopulmonary Bypass/adverse effects , Potassium Chloride
8.
Molecules ; 29(12)2024 Jun 13.
Article in English | MEDLINE | ID: mdl-38930884

ABSTRACT

Acute lung injury (ALI) remains a significant global health issue, necessitating novel therapeutic interventions. In our latest study, we pioneered the use of D-mannitol-cerium-quercetin/rutin coordination polymer nanoparticles (MCQ/R NPs) as a potential treatment for ALI. The MCQ/R NPs, which integrate rutin and quercetin for their therapeutic potential and D-mannitol for its pulmonary targeting, displayed exceptional efficacy. By utilizing cerium ions for optimal nanoparticle assembly, the MCQ/R NPs demonstrated an average size of less than 160 nm. Impressively, these nanoparticles outperformed conventional treatments in both antioxidative capabilities and biocompatibility. Moreover, our in vivo studies on LPS-induced ALI mice showed a significant reduction in lung tissue inflammation. This groundbreaking research presents MCQ/R NPs as a promising new approach in ALI therapeutics.


Subject(s)
Acute Lung Injury , Cerium , Mannitol , Nanoparticles , Polymers , Quercetin , Acute Lung Injury/drug therapy , Quercetin/pharmacology , Quercetin/chemistry , Animals , Mannitol/chemistry , Mannitol/therapeutic use , Nanoparticles/chemistry , Mice , Polymers/chemistry , Cerium/chemistry , Cerium/pharmacology , Cerium/therapeutic use , Rutin/chemistry , Rutin/pharmacology , Rutin/therapeutic use , Antioxidants/pharmacology , Antioxidants/chemistry , Humans , Drug Synergism , Disease Models, Animal , Lipopolysaccharides
9.
Eur J Emerg Med ; 31(4): 287-293, 2024 Aug 01.
Article in English | MEDLINE | ID: mdl-38691014

ABSTRACT

BACKGROUND AND IMPORTANCE: Occurrence of mydriasis during the prehospital management of traumatic brain injury (TBI) may suggest severe intracranial hypertension (ICH) subsequent to brain herniation. The initiation of hyperosmolar therapy to reduce ICH and brain herniation is recommended. Whether mannitol or hypertonic saline solution (HSS) should be preferred is unknown. OBJECTIVES: The objective of this study is to assess whether HSS, compared with mannitol, is associated with improved survival in adult trauma patients with TBI and mydriasis. DESIGN/SETTING AND PARTICIPANTS: A retrospective observational cohort study using the French Traumabase national registry to compare the ICU mortality of patients receiving either HSS or mannitol. Patients aged 16 years or older with moderate to severe TBI who presented with mydriasis during prehospital management were included. OUTCOME MEASURES AND ANALYSIS: We performed propensity score matching on a priori selected variables [i.e. age, sex and initial Coma Glasgow Scale (GCS)] with a ratio of 1 : 3 to ensure comparability between the two groups. The primary outcome was ICU mortality. The secondary outcomes were regression of pupillary abnormality during prehospital management, pulsatility index and diastolic velocity on transcranial Doppler within 24 h after TBI, early ICU mortality (within 48 h), ICU and hospital length of stay. RESULTS: Of 31 579 patients recorded in the registry between 2011 and 2021, 1417 presented with prehospital mydriasis and were included: 1172 (82.7%) received mannitol and 245 (17.3%) received HSS. After propensity score matching, 720 in the mannitol group matched 240 patients in the HSS group. Median age was 41 years [interquartile ranges (IQR) 26-60], 1058 were men (73%) and median GCS was 4 (IQR 3-6). No significant difference was observed in terms of characteristics and prehospital management between the two groups. ICU mortality was lower in the HSS group (45%) than in the mannitol group (54%) after matching [odds ratio (OR) 0.68 (0.5-0.9), P  = 0.014]. No differences were identified between the groups in terms of secondary outcomes. CONCLUSION: In this propensity-matched observational study, the prehospital osmotherapy with HSS in TBI patients with prehospital mydriasis was associated with a lower ICU mortality compared to osmotherapy with mannitol.


Subject(s)
Brain Injuries, Traumatic , Emergency Medical Services , Mannitol , Humans , Mannitol/therapeutic use , Mannitol/administration & dosage , Saline Solution, Hypertonic/therapeutic use , Saline Solution, Hypertonic/administration & dosage , Brain Injuries, Traumatic/complications , Brain Injuries, Traumatic/mortality , Brain Injuries, Traumatic/therapy , Female , Male , Retrospective Studies , Middle Aged , Adult , Emergency Medical Services/methods , France , Glasgow Coma Scale , Registries , Propensity Score , Cohort Studies , Intracranial Hypertension/etiology , Intracranial Hypertension/drug therapy , Intracranial Hypertension/therapy , Aged , Diuretics, Osmotic/therapeutic use
10.
Sci Rep ; 14(1): 10511, 2024 05 07.
Article in English | MEDLINE | ID: mdl-38714773

ABSTRACT

Cisplatin (CDDP)-induced nephrotoxicity is a common dose-limiting toxicity, and diuretics are often administered to prevent nephrotoxicity. However, the efficacy and optimal administration of diuretics in preventing CDDP-induced nephrotoxicity remain to be established. This study aimed to evaluate the efficacy of combining furosemide and mannitol to prevent CDDP-induced nephrotoxicity. This was a post-hoc analysis of pooled data from a multicenter, retrospective, observational study, including 396 patients who received one or two diuretics for CDDP-based chemotherapy, compared using propensity score matching. Multivariate logistic regression analyses were used to identify risk factors for nephrotoxicity. There was no significant difference in the incidence of nephrotoxicity between the two groups (22.2% vs. 28.3%, P = 0.416). Hypertension, CDDP dose ≥ 75 mg/m2, and no magnesium supplementation were identified as risk factors for nephrotoxicity, whereas the use of diuretics was not found to be a risk factor. The combination of furosemide and mannitol showed no advantage over a single diuretic in preventing CDDP-induced nephrotoxicity. The renal function of patients receiving CDDP-based chemotherapy (≥ 75 mg/m2) and that of those with hypertension should be carefully monitored. Magnesium supplementation is important for these patients.


Subject(s)
Cisplatin , Diuretics , Furosemide , Mannitol , Furosemide/adverse effects , Furosemide/administration & dosage , Cisplatin/adverse effects , Humans , Mannitol/therapeutic use , Mannitol/administration & dosage , Male , Female , Diuretics/administration & dosage , Diuretics/adverse effects , Diuretics/therapeutic use , Middle Aged , Retrospective Studies , Aged , Risk Factors , Kidney Diseases/chemically induced , Kidney Diseases/prevention & control , Drug Therapy, Combination , Antineoplastic Agents/adverse effects , Adult
11.
World Neurosurg ; 187: e352-e362, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38663735

ABSTRACT

OBJECTIVE: Osmotherapeutic agents increase the intravascular volume by withdrawing water from the brain followed by relative hypovolemia due to diuresis leading to significant changes in systemic hemodynamics which might have adverse consequences in the elderly. We studied the effect of mannitol (20%) and hypertonic saline (HTS) (3%) on left ventricular outflow tract velocity time integral (LVOT-VTI) and cardiac output (CO) in elderly patients undergoing supratentorial neurosurgical procedures using transesophageal echocardiography. METHODS: We recruited 28 patients aged above 65 years undergoing supratentorial craniotomy who received equiosmolar solutions of 5.35 ml/kg of 3% HTS (group HS, n = 14) or 5 ml/kg of 20% mannitol (group M, n = 14). LVOT-VTI was recorded at baseline, 15, 30, 45, 60, and 90 minutes postinfusion and CO was derived. We also recorded heart rate, blood pressure, fluid balance, brain relaxation, vasopressor use, complications, and neurological outcome. RESULTS: We found a significant decrease in LVOT-VTI at 45, and 60 minutes in group M as compared to group HS [mean (standard deviation), 16.76 (1.81) vs. 20.78 (1.87), P < 0.001, 17.4 (2.38) vs. 19.16 (2), P = 0.044, respectively]. We also found a corresponding significant fall in CO [3863.16 (845.87) vs. 4745.59 (1209.33) ml/minute, P = 0.034] and systolic blood pressure (P = 0.039), at 45 minutes in group M. Urine output was higher in group M (P < 0.001). All other parameters were comparable. CONCLUSIONS: HTS appears to be associated with better systemic hemodynamics (LVOT-VTI, CO) while providing equivalent brain relaxation as mannitol in elderly patients. A future larger study is required to confirm our preliminary findings.


Subject(s)
Echocardiography, Transesophageal , Mannitol , Humans , Aged , Mannitol/therapeutic use , Mannitol/administration & dosage , Saline Solution, Hypertonic/therapeutic use , Female , Male , Echocardiography, Transesophageal/methods , Neurosurgical Procedures/methods , Cardiac Output/drug effects , Cardiac Output/physiology , Hemodynamics/drug effects , Craniotomy/methods , Aged, 80 and over , Diuretics, Osmotic/therapeutic use , Blood Pressure/drug effects
12.
Eur J Cardiothorac Surg ; 65(4)2024 Mar 29.
Article in English | MEDLINE | ID: mdl-38627243

ABSTRACT

OBJECTIVES: In this study, we evaluated if modified Del Nido cardioplegia delivers comparable cardiac protection in comparison to Custodiol® in patients undergoing isolated minimally invasive mitral valve repair. METHODS: From January 2018 to October 2021, all patients undergoing non-emergent isolated minimally invasive mitral valve repair were included in this study. The cardioplegia was chosen at the surgeons' discretion. The primary end points of this study were peak postoperative cardiac enzyme levels. Secondary end points were in-hospital mortality, hospital stay, occurrence of cardiac arrhythmias, pacemaker implantations, postoperative lactate and sodium levels and postoperative incidence of renal failure requiring dialysis. RESULTS: A total of 355 patients were included in this study. The mean age of patients was 57. After propensity score matching, a total of 156 pairs were identified. There was no difference in cross-clamp time between both groups. Postoperative creatine kinase levels were higher in patients receiving Custodiol on the 1st and 2nd postoperative days. Creatine kinase isoenzyme MB levels were higher in patients receiving Custodiol on the 2nd postoperative day (0.5 ± 0.2 vs 0.4 ± 0.1 µmol/l s; P < 0.001). Postoperative Troponin T concentrations were similar between both groups. Maximum lactate concentrations were higher in patients receiving Custodiol on the day of surgery (2.4 ± 1.9 vs 2.0 ± 1.1 mmol/l; P = 0.04). The overall hospital stay was longer in patients receiving Del Nido cardioplegia (10.6 ± 3.2 vs 8 ± 4.1 days; P < 0.01). CONCLUSIONS: Modified Del Nido cardioplegia based on Ionosteril® solution offers equivalent protection compared to Custodiol for isolated minimally invasive mitral valve repair.


Subject(s)
Cardioplegic Solutions , Electrolytes , Heart Arrest, Induced , Lidocaine , Minimally Invasive Surgical Procedures , Mitral Valve , Potassium Chloride , Procaine , Sodium Bicarbonate , Solutions , Humans , Female , Male , Middle Aged , Heart Arrest, Induced/methods , Cardioplegic Solutions/therapeutic use , Mitral Valve/surgery , Potassium Chloride/therapeutic use , Minimally Invasive Surgical Procedures/methods , Mannitol/therapeutic use , Glucose/administration & dosage , Aged , Histidine , Retrospective Studies , Postoperative Complications/prevention & control , Calcium Chloride/administration & dosage , Mitral Valve Insufficiency/surgery , Magnesium Sulfate/therapeutic use
13.
Neurosurgery ; 95(3): 517-526, 2024 Sep 01.
Article in English | MEDLINE | ID: mdl-38551382

ABSTRACT

BACKGROUND AND OBJECTIVES: The preferred osmotic agent used for brain relaxation during craniotomies remains unclear, either mannitol (MAN) or hypertonic saline (HTS). Hence, we sought to compare these solutions in this population. METHODS: MEDLINE, Embase, and Cochrane databases were systematically searched until August 02, 2023. Data were examined using the Mantel-Haenszel method and 95% CIs. Heterogeneity was assessed using I2 statistics. Meta-regression analysis was conducted to evaluate a possible link between Brain Relaxation Score and tumor volume. R, version 4.2.3, was used for statistical analysis. RESULTS: A total of 16 randomized controlled trials and 1031 patients were included, of whom 631 (61%) underwent surgery for supratentorial tumor resection. Compared with MAN, HTS achieved better rates of brain relaxation (80% vs 71%; odds ratio [OR] 1.68; 95% CI 1.22-2.33; P = .001; I2 = 0%), which was also demonstrated in the subgroup analysis of patients with supratentorial brain tumor (78% vs 65%; OR 2.02; 95% CI 1.36-2.99; P = .0005; I2 = 0%); a minor number of patients requiring a second dose of osmotic agent (14% vs 28%; OR 0.43; 95% CI 0.27-0.69; P = .0003; I2 = 0%); a lower fluid intake (mean difference -475.9341 mL; 95% CI -818.8952 to -132.9730; P = .007; I2 = 88%); and lower urine output (mean difference -462.0941 mL; 95% CI -585.3020 to -338.8862; P = <.001; I2 = 96%). Hospital length of stay and focal neurological deficits did not reach a statistically significant difference between groups. CONCLUSION: In this updated meta-analysis, consistent results suggest that HTS is associated with more beneficial outcomes than MAN in patients undergoing craniotomy.


Subject(s)
Craniotomy , Mannitol , Humans , Saline Solution, Hypertonic/administration & dosage , Mannitol/administration & dosage , Mannitol/therapeutic use , Craniotomy/methods , Supratentorial Neoplasms/surgery , Brain/surgery , Brain/drug effects , Randomized Controlled Trials as Topic/methods , Brain Neoplasms/surgery
14.
Neuropharmacology ; 251: 109896, 2024 Jun 15.
Article in English | MEDLINE | ID: mdl-38490299

ABSTRACT

Secondary brain injury after intracerebral hemorrhage (ICH) is the main cause of poor prognosis in ICH patients, but the underlying mechanisms remain less known. The involvement of Piezo1 in brain injury after ICH was studied in a mouse model of ICH. ICH was established by injecting autologous arterial blood into the basal ganglia in mice. After vehicle, Piezo1 blocker, GsMTx4, Piezo1 activator, Yoda-1, or together with mannitol (tail vein injection) was injected into the left lateral ventricle of mouse brain, Piezo1 level and the roles of Piezo1 in neuronal injury, brain edema, and neurological dysfunctions after ICH were determined by the various indicated methods. Piezo1 protein level in neurons was significantly upregulated 24 h after ICH in vivo (human and mice). Piezo1 protein level was also dramatically upregulated in HT22 cells (a murine neuron cell line) cultured in vitro 24 h after hemin treatment as an in vitro ICH model. GsMTx4 treatment or together with mannitol significantly downregulated Piezo1 and AQP4 levels, markedly increased Bcl2 level, maintained more neurons alive, considerably restored brain blood flow, remarkably relieved brain edema, substantially decreased serum IL-6 level, and almost fully reversed the neurological dysfunctions at ICH 24 h group mice. In contrast, Yoda-1 treatment achieved the opposite effects. In conclusion, Piezo1 plays a crucial role in the pathogenesis of brain injury after ICH and may be a target for clinical treatment of ICH.


Subject(s)
Brain Edema , Brain Injuries , Pyrazines , Thiadiazoles , Humans , Mice , Animals , Cerebral Hemorrhage/complications , Brain Injuries/drug therapy , Ion Channels , Brain Edema/metabolism , Mannitol/therapeutic use
15.
Curr Oncol Rep ; 26(3): 236-249, 2024 03.
Article in English | MEDLINE | ID: mdl-38329660

ABSTRACT

PURPOSE OF REVIEW: To review relevant advances in the past half-decade in the treatment of primary brain tumors via modification of blood-brain barrier (BBB) permeability. RECENT FINDINGS: BBB disruption is becoming increasingly common in the treatment of primary brain tumors. Use of mannitol in BBB disruption for targeted delivery of chemotherapeutics via superselective intra-arterial cerebral infusion (SIACI) is the most utilized strategy to modify the BBB. Mannitol is used in conjunction with chemotherapeutics, oligonucleotides, and other active agents. Convection-enhanced delivery has become an attractive option for therapeutic delivery while bypassing the BBB. Other technologic innovations include laser interstitial thermal therapy (LITT) and focused ultrasound (FUS) which have emerged as prime modalities to directly target tumors and cause significant local BBB disruption. In the past 5 years, interest has significantly increased in studying modalities to disrupt the BBB in primary brain tumors to enhance treatment responses and improve clinical outcomes.


Subject(s)
Blood-Brain Barrier , Brain Neoplasms , Humans , Blood-Brain Barrier/pathology , Brain/pathology , Mannitol/therapeutic use , Drug Delivery Systems , Brain Neoplasms/diagnostic imaging , Brain Neoplasms/drug therapy
16.
J Oral Maxillofac Surg ; 82(5): 572-580, 2024 May.
Article in English | MEDLINE | ID: mdl-38387857

ABSTRACT

BACKGROUND: The removal of the lower third molar is a routine procedure in oral surgery, yet it often leads to postoperative side effects, particularly inflammation. Despite various interventions explored in prior studies, there is still a need for effective strategies, such as anti-inflammatory substances, to address postoperative side effects. PURPOSE: The purpose of this study is to answer the following clinical question: Does the local injection of 0.9 M mannitol reduce postoperative pain, trismus, and swelling in patients undergoing bilateral symmetrically impacted mandibular third molar extraction? STUDY DESIGN, SETTING, SAMPLE: This prospective, single-blind, split-mouth study at Hamadan Dental School involved 30 patients with bilateral symmetrically impacted mandibular third molars. Inclusion criteria were: no current medication, no anesthesia allergies, bilateral symmetrically impacted mandibular third molars, non-smokers, and the absence of systemic diseases. Exclusion criteria were: poor oral hygiene, alcohol/cigarette use, drug consumption, diabetes, systemic/gastrointestinal disorders, infection at the surgical site, lack of patient cooperation, and mannitol/anesthetic allergy. PREDICTOR/EXPOSURE/INDEPENDENT VARIABLE: The predictor variable was therapeutic injection, and it was grouped into two categories, 0.9 M mannitol solution or distilled water. MAIN OUTCOME VARIABLE: The primary outcome variable was pain. Secondary outcomes are trismus, swelling, patient satisfaction, and analgesic consumption. COVARIATES: Covariates included demographic information and operative details. ANALYSES: Statistical analyses included repeated measures and paired t-tests with a significance level set at P < .05. RESULTS: The study comprised 30 participants (mean age: 22.6 ± 3.59 years; 6 men, 24 women). In the test group, pain intensity significantly decreased from 5.30 on surgery day to 0.00, with subsequent values of 2.97, 1.30, 0.40, 0.17, and 0.03. The control group also decreased from 7.68 to 0.00, with values of 4.73, 2.67, 0.97, 0.23, and 0.07. The difference was statistically significant (P < .001). No significant swelling differences at T1, T3, T5, and T7 (P > .05). The intervention group had improved maximum mouth opening at T1, T3, T5, and T7 (P = .011) compared to the control group. CONCLUSION AND RELEVANCE: Mannitol infiltration significantly reduces postoperative pain and trismus in impacted third molar surgery. This finding underscores the potential for improved patient comfort and recovery in this context.


Subject(s)
Mannitol , Molar, Third , Pain, Postoperative , Tooth Extraction , Tooth, Impacted , Trismus , Humans , Trismus/prevention & control , Trismus/etiology , Molar, Third/surgery , Tooth, Impacted/surgery , Pain, Postoperative/prevention & control , Mannitol/therapeutic use , Mannitol/administration & dosage , Female , Male , Prospective Studies , Adult , Tooth Extraction/adverse effects , Single-Blind Method , Young Adult , Mandible/surgery , Pain Measurement , Adolescent
17.
J Allergy Clin Immunol Pract ; 12(4): 904-907, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38097177

ABSTRACT

Airway hyper-responsiveness (AHR) is a tenet of the persistent asthma phenotype along with reversible airway obstruction and type 2 (T2) inflammation. Indirect acting challenges such as mannitol are more closely related to the underlying T2 inflammatory process as compared with direct challenges. In this review article, we summarise the current literature and explore the future role of mannitol AHR in clinical remission with biologics.


Subject(s)
Asthma , Respiratory Hypersensitivity , Humans , Asthma/drug therapy , Inflammation , Biological Therapy , Mannitol/therapeutic use
18.
Sichuan Da Xue Xue Bao Yi Xue Ban ; 54(5): 1040-1045, 2023 Sep.
Article in Chinese | MEDLINE | ID: mdl-37866966

ABSTRACT

Objective: To analyze the application effect of continuous lumbar cistern fluid drainage combined with decompressive craniectomy in the treatment of severe craniocerebral injury. Methods: A total of 87 patients with severe craniocerebral injury admitted to our hospital between March 2016 and March 2021 were retrospectively enrolled. They were divided into two groups according to the decompression methods applied, with 42 patients who received standard decompressive craniectomy assigned to the control group and 45 patients who received continuous lumbar cistern fluid drainage combined with standard decompressive craniectomy assigned to the observation group. The primary indicators that were monitored and compared between the two group included the amount of time for patient CT imaging to be clear of subarachnoid hemorrhage, the length-of-stay, the duration of post-operative intubation, the mannitol dose, scores for Glasgow Coma Scale (GCS), prognosis, the incidence of cerebral edema and cerebral infarction, and complications. The secondary indicators that were monitored and compared included intracranial pressure, cerebrospinal fluid antinucleosome protein SP100, and red blood cell count of the two groups before treatment and after continuous drainage for 7 days. Results: The amount of time for CT imaging to be clear of subarachnoid hemorrhage and the length-of-stay of the observation group were shorter than those of the control group, the mannitol dose of the observation group was lower than that of the control group, the incidence of cerebral edema and the incidence of complications of the observation group were lower than those of the control group, and the rate of patients with good prognosis in the observation group was higher than that in the control group ( P<0.05). There was no significant difference in the rate of poor prognosis or mortality between the two groups ( P>0.05). The duration of postoperative intubation of the observation group was (8.24±1.09) d, while that of the control group was (9.22±1.26) d, and the difference between the two groups was statistically significant ( t=3.887, P<0.05). There were 2 cases (4.44%) of cerebral infarction in the observation group, with the infarct volume being (8.36±1.87) cm 3, while there were 9 cases (21.43%) of cerebral infarction in the control group, with the infarct volume being (8.36±1.87) cm 3, and there were statistically significant differences in the incidence and volume of cerebral infarction between the two groups ( χ 2=5.674, t=9.609, P<0.05). After treatment, the intracranial pressure and red blood cell count decreased in both groups and the intracranial pressure, cerebrospinal fluid SP100, and red blood cell count of the observation group were significantly lower than those of the control group ( P<0.05). The cerebrospinal fluid SP100 of the observation group decreased after treatment in comparison with the level before treatment ( P<0.05), while the pre- and post-treatment levels of the control group did not demonstrate any significant difference. Conclusion: Continuous lumbar cistern fluid drainage in patients with severe craniocerebral injury effectively shortens the time required for the body to recover, significantly reduces the level of intracranial pressure, improves the levels of cerebral edema and cerebral infarction, and has a high degree of safety for prognosis and recovery.


Subject(s)
Brain Edema , Craniocerebral Trauma , Decompressive Craniectomy , Subarachnoid Hemorrhage , Humans , Decompressive Craniectomy/methods , Brain Edema/etiology , Subarachnoid Hemorrhage/surgery , Subarachnoid Hemorrhage/drug therapy , Retrospective Studies , Treatment Outcome , Craniocerebral Trauma/drug therapy , Craniocerebral Trauma/surgery , Drainage/methods , Mannitol/therapeutic use , Cerebral Infarction/drug therapy , Cerebral Infarction/surgery
19.
World Neurosurg ; 180: e163-e170, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37696434

ABSTRACT

OBJECTIVE: A topic of current research is the development of a new approach to the diagnosis and treatment of severe brain injury taking into consideration its main pathophysiological mechanism-idiopathic intracranial hypertension syndrome. The goal of this study was to identify Doppler patterns of unfavorable craniocerebral injury conditions to form a consistent algorithm of treatment measures to reduce secondary brain damage in patients with severe craniocerebral trauma. METHODS: Transcranial Doppler imaging is a prospective method, which allows quick and noninvasive assessment of the intracerebral blood flow dynamics right at the patient's bedside. Due to the operator-dependent nature of this method, clinical interpretation can often be contradictory. As a result, no clear criteria for therapy correction have yet been formulated based on this neuroimaging method. RESULTS: Analysis of the therapy performed allowed us to specify the options for the hyperosmolar solutions for the correction of idiopathic intracranial hypertension syndrome. CONCLUSIONS: No statistically significant difference in effectiveness was shown between mannitol and hypertonic saline solutions.


Subject(s)
Brain Injuries, Traumatic , Brain Injuries , Intracranial Hypertension , Pseudotumor Cerebri , Humans , Pseudotumor Cerebri/complications , Pseudotumor Cerebri/diagnostic imaging , Pseudotumor Cerebri/therapy , Intracranial Hypertension/diagnosis , Intracranial Hypertension/etiology , Intracranial Hypertension/therapy , Brain Injuries, Traumatic/complications , Brain Injuries, Traumatic/diagnostic imaging , Brain Injuries, Traumatic/therapy , Mannitol/therapeutic use , Brain Injuries/complications , Saline Solution, Hypertonic , Intracranial Pressure
20.
Br J Hosp Med (Lond) ; 84(6): 1-2, 2023 Jun 02.
Article in English | MEDLINE | ID: mdl-37364885

ABSTRACT

Despite extensive study and use, selecting an osmotherapy agent for traumatic brain injury remains a dilemma. This article explores the challenges in managing patients with traumatic brain injury and the ongoing debate surrounding the efficacy of different hyperosmolar agents as treatment options.


Subject(s)
Brain Edema , Brain Injuries, Traumatic , Humans , Mannitol/therapeutic use , Saline Solution, Hypertonic/therapeutic use , Brain Injuries, Traumatic/drug therapy
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