Category: Statistics

Eur J Dent. 2021 Sep 29. doi: 10.1055/s-0041-1732802. Online ahead of print.

ABSTRACT

OBJECTIVE: This study aimed to investigate the impact of mechanical complications on outcome measures for implant dentistry.

MATERIALS AND METHODS: This case-control study included 282 patients with mechanical complications occurring in fixed prosthetic rehabilitation supported by immediate function implants with external connection (cases) and 282 individuals without mechanical complications (control). Pairing was performed for sex, age (range = 3 years), and follow-up months (range = 11 months). The primary outcome measure was implant survival, while the secondary outcome measures were marginal bone loss and biological complication parameters (peri-implant pathology, soft tissue inflammation, fistula formation, and abscess formation).

STATISTICAL ANALYSIS: Cumulative implant survival was estimated by using life tables. Descriptive statistics with 95% confidence intervals (CI) and inferential statistics (Chi-square test) were performed to evaluate differences between cases and controls. The significance level was set at 5%.

RESULTS: The average follow-up duration was 8.5 years. Mechanical complications included prosthetic fracture (n = 159), abutment loosening (n = 89), prosthetic screw loosening (n = 20), milled abutment (n = 12), milled prosthetic screw (n = 1), and decemented crown (n = 1). Implant failure occurred in one patient from the control group, with survival rates of 100 and 99.6% for cases and controls, respectively (p = 0.317). The average marginal bone loss was 1.72 (95% confidence interval [CI]: 1.60-1.84) for cases and 1.55 (95% CI: 1.45-1.65) for controls (p = 0.068). Biological complications were observed in 90 patients, with significant differences between cases (n = 54) and controls (n = 36; p = 0.038).

CONCLUSION: Mechanical complications did not significantly influence survival or marginal bone loss; nevertheless, there is a need for studies with longer follow-up duration. Mechanical complications also significantly influence the incidence of biological complications.

PMID:34587636 | DOI:10.1055/s-0041-1732802

Interact Cardiovasc Thorac Surg. 2021 Sep 29:ivab259. doi: 10.1093/icvts/ivab259. Online ahead of print.

ABSTRACT

OBJECTIVES: This study investigated the efficacy and complications of albendazole use after surgery in patients with pulmonary hydatid cysts.

METHODS: One hundred fifty-three consecutive patients who met the study criteria out of 215 patients who received prophylaxis with albendazole after surgery for isolated pulmonary hydatid cysts in our clinic between January 2011 and December 2020 were analysed retrospectively.

RESULTS: Eighty-six out of 153 (56.2%) of cases were male and 67 (43.8%) were female. The average age was 24.6 ± 17.4 (between 3 and 71 years), 76 of them (49.7%) were 18 years old and younger, while 77 (50.3%) were adults. All cases were approached transthoracically and a total of 170 operations were performed on the 153 cases. Fever, weakness and dizziness were reported in only one patient who was given albendazole treatment. A partial increase in liver enzymes was observed in 16 cases (10.5%) after albendazole treatment. Mild leukopoenia and neutropenia were observed in only one of the cases. In 1 case, a second operation was performed 30 months later due to recurrence. Albendazole treatment was not required to be discontinued in any of the cases. Mortality was not observed in any of the cases. Factors such as mean age, cyst size and hospitalization period did not have a statistically significant effect on any changes in liver enzymes tests following albendazole therapy (P > 0.05).

CONCLUSIONS: Albendazole treatment can safely be used for postoperative prophylaxis in patients with pulmonary hydatid cysts in a controlled manner without causing serious complications.

SUBJ COLLECTION: 152.

PMID:34587626 | DOI:10.1093/icvts/ivab259

Klin Monbl Augenheilkd. 2021 Sep 29. doi: 10.1055/a-1579-0805. Online ahead of print.

ABSTRACT

BACKGROUND: The aim of the study was to assess retinal microcirculation in patients with coronavirus disease 2019 (COVID-19) through the use of optical coherence tomography angiography (OCT-A) and compare the results with those obtained in healthy controls.

METHODS: The study enrolled 39 patients who had fully recovered from COVID-19 and 40 healthy controls. OCT-A image acquisitions were obtained using AngioVue software (version 2017.1.0.151) and the RTVue XR Avanti imaging system (Optovue Inc., Fremont, CA, USA). Nonflow area in the superficial capillary plexus (SCP), foveal avascular zone (FAZ) area in the whole retinal vasculature, FAZ perimeter, acircularity index of FAZ, and foveal density were automatically obtained with the FAZ assessment tool. Vessel density (VD) at the SCP and deep capillary plexus were also measured.

RESULTS: Compared to the control group, the nonflow area and the FAZ area in the whole retina was greater in the COVID-19 group; however no statistically significant difference was observed (p > 0.05 respectively). As for vessel densities, all superficial parafoveal VD parameters were considerably higher in the COVID-19 group compared to the control group (p < 0.05 respectively). Despite the fact that the vessel densities in the remaining zones were lower in the COVID-19 group, those differences were not statistically significant (p > 0.05 respectively).

CONCLUSION: VD at the parafoveal area of the SCP was significantly higher among patients in the late post-recovery period of COVID-19 disease compared to healthy controls. These findings show the impact of COVID-19 on the retinal microvasculature and its possible role as a risk factor for the development of ocular diseases.

PMID:34587629 | DOI:10.1055/a-1579-0805

Int Immunopharmacol. 2021 Sep 16;100:108136. doi: 10.1016/j.intimp.2021.108136. Online ahead of print.

ABSTRACT

BACKGROUND: Healthcare professionals (HCPs) are at the front line of the nation’s fight against COVID-19 and are always at a greater risk of contracting contagious disease. But amidst the crisis, the vaccines were not accepted by all the HCPs due to adverse events occurring post-COVID-19 vaccination. Hence, the present study was designed to assess adverse events occurring among HCPs post-COVID-19 vaccination both quantitatively and qualitatively.

METHOD: Sequential mixed-method approach was employed. A cross-sectional E-survey was conducted among the healthcare professionals of a North Indian (*Statistically significant (p < 0.05)) college and hospital. The second phase included a semi-structured qualitative interview of the participants who were willing to participate.

RESULTS: Among all the HCPs with age groups ranging from 20 to 70 years, majority of them experienced pain at the site of injection (88.8-100%) followed by tiredness (87.7-60%) and body ache (86.6-40%) post-vaccination. There is an increased frequency of adverse events in females as compared to males. Qualitative findings are summarised in three major domains i.e vaccine adverse effects, fear and hesitancy for vaccines and vaccine acceptance.

CONCLUSION: Short term adverse events of COVISHIELD vaccine were very few and were mild in severity yet interviews showed hesitancy of study participants for vaccination.

PMID:34587578 | DOI:10.1016/j.intimp.2021.108136

Phys Med Biol. 2021 Sep 29. doi: 10.1088/1361-6560/ac2b80. Online ahead of print.

ABSTRACT

Modern radiotherapy stands to benefit from the ability to efficiently adapt plans during treatment in response to setup and geometric variations such as those caused by internal organ deformation or tumor shrinkage. A promising strategy is to develop a framework, which given an initial state defined by patient-attributes, can predict future states based on patterns from a well-defined patient population. Here, we investigate the feasibility of predicting patient anatomical changes, defined as a joint state of volume and daily setup changes, across a fractionated treatment schedule using two approaches. The first is based on a new framework employing quantum mechanics in combination with deep recurrent neural networks, denoted QRNN. The second approach is developed based on a classical framework, which models patient changes as a Markov process, denoted MRNN. We evaluated the performance of these two approaches on a dataset of 125 head and neck cancer patients, which was supplemented by synthetic data generated using a generative adversarial network. Model performance was evaluated using area under the receiver operating characteristic curve (AUC) scores. The MRNN framework had slightly better performance, with MRNN(QRNN) validation AUC scores of 0.742 ± 0.021 (0.675 ± 0.036), 0.709 ± 0.026 (0.656 ± 0.021), 0.724 ± 0.036 (0.652 ± 0.044), and 0.698 ± 0.016 (0.605 ± 0.035) for system state vector sizes of 4, 6, 8, and 10, respectively. Of these, the results from the two higher order states had statistically significant differences (p<0.05). A similar trend was observed when the models were applied to an external testing dataset of 20 patients, yielding MRNN(QRNN) AUC scores of 0.707 (0.623), 0.687 (0.608), 0.723 (0.669), and 0.697 (0.609) for states vectors sizes of 4, 6, 8, and 10, respectively. These results suggest that both models have potential value in predicting patient changes during the course of adaptive radiotherapy.

PMID:34587597 | DOI:10.1088/1361-6560/ac2b80

Psychiatry Res. 2021 Sep 5;305:114204. doi: 10.1016/j.psychres.2021.114204. Online ahead of print.

ABSTRACT

Given the importance of the cerebellum in the pathophysiology of schizophrenia, the cerebellar vermis has been proposed as a new rTMS stimulation site for negative symptoms. In this study, 64 patients from 7 psychiatric hospitals were randomized into the study (n=32) or control (n=32) group. Intermittent theta burst stimulation (iTBS) (or sham stimulation) to the cerebellar midline was administered 5 times/week for 2 weeks. Psychotic symptoms were assessed with the Positive and Negative Symptoms Scale (PANSS) at baseline, the end of treatment, and 2, 6, 12, and 24 weeks after the treatment. Regarding the negative symptoms, the interaction effect between group and time was statistically significant, with the scores in the study group significantly lower than those in the control group at the 4 follow-ups after treatment, and the group difference was maximal at 24 weeks of follow-up. The main effect of time was significant; however, the main effect of group did not show statistical significance. Our study revealed that cerebellar iTBS may improve negative symptoms in schizophrenia patients, and the effect was more pronounced at 24 weeks after the end of treatment, which provides preliminary empirical evidence for the maintenance of efficacy after stimulation of this new site.

PMID:34587567 | DOI:10.1016/j.psychres.2021.114204

J Pharm Biomed Anal. 2021 Sep 20;206:114383. doi: 10.1016/j.jpba.2021.114383. Online ahead of print.

ABSTRACT

The dubious online market in phosphodiesterase type 5 inhibitors is growing on a global scale. Counterfeit medical products can represent health issues for the user and cause medical mistrust. Within this work, genuine Cialis containing the active pharmaceutical ingredient (API) tadalafil, its generics available in the Czech Republic and the Cialis tablets from questionable online pharmacies were analysed. The methods of infra-red and Raman spectroscopy were used for the identification of the counterfeit tablets and for the verification of their API and excipients. All 9 tablets from online pharmacies were counterfeit with 2 of them even containing a different API (sildenafil, vardenafil). In addition, Raman mapping was used to determine the API and excipients’ distribution and, in combination with multivariate data analysis, to separate similar tablets in clusters and to identify the outliers. Scanning electron microscopy of the samples revealed that the process of a wet granulation of micronized API was used during the formulation of the tablets. This comprehensive approach of analysis can be used for advanced exploration of the dubious samples of various medical products.

PMID:34587570 | DOI:10.1016/j.jpba.2021.114383

Forensic Sci Int. 2021 Sep 22;328:111012. doi: 10.1016/j.forsciint.2021.111012. Online ahead of print.

ABSTRACT

INTRODUCTION: The presence of anabolic-androgenic steroids (AAS) in illegal commercial products has been pointed as a global threat for public health. Due the correlation with adverse toxicological effects, there is a growing interest in the implementation of straightforward methods for the determination of AAS in seized products. This work exploited the development of a mass spectrometry approach to characterize the illegal oil formulations containing AAS.

METHODS: The optimization of sample preparation was performed through a simplex-centroid design and the best condition was described as follow: an aliquot of 5 μL of sample were added with 995 μL of acetonitrile and water (75:25, v/v). The solution was vortexed and centrifuged. After that, 10 μL of supernatant were added with 35 μL of acetonitrile and water and internal standard (testosterone-d₃, 1.25 ng). An aliquot of 5 μL was injected into the analytical system.

RESULTS: The method developed was validated and successfully applied in 115 seized samples. Testosterone and its esters had the highest incidence, found in more than 50% of the samples. Besides that, drugs such as boldenone, methandienone, and trenbolone have also been found, where the low quality of the samples was evidenced by the wide variation in the concentration of the drugs, always quantified in sub-doses. Finally, at least one AAS was detected in each sample analyzed. The statistical results were grouped by principal components analysis, to better understand the profile of the seized samples.

CONCLUSION: This work successfully established a fast and simple method for determination of AAS and can be applied to verify the profile of seized samples.

PMID:34587560 | DOI:10.1016/j.forsciint.2021.111012

Comput Methods Programs Biomed. 2021 Sep 10;211:106410. doi: 10.1016/j.cmpb.2021.106410. Online ahead of print.

ABSTRACT

PURPOSE: The characteristics of children’s reading interest, stimulated by the visual evoked potentials of colour graphics in children’s picture books, were tested to explore their normal reference value. The characteristics of chromatic pattern visual evoked potential (CP-VEP) can be harnessed by our methodology and may be applied to the visual screening of children in clinical ophthalmology.

METHODS: The PR-650 spectral colour metre can strictly control factors, such as brightness and colour retention, based on colour contrast. This is performed in order to reduce the brightness contrast method. In our paper, we set up three kinds of visual stimulation conditions and performed CP-VEP inspections of the eye, based on 64 cases (128 eyes) of normal children (32 males and 32 females). Using CP-VEP detection, the latency and amplitude of the P100 wave were recorded and the waveforms of each group, under different spectral modes were compared. Art therapy combined with children’s colour physiology and psychology will be more skilfully practiced in clinical practice.

RESULTS: There was no significant difference in the amplitude and peak time of visual evoked potential (VEP) waveforms between the left and right eyes of the children using the three stimuli, indicating that the visual function and visual conduction pathway of children can vary. There was no significant difference in the latency and amplitude of the NPN complex wave. Note that the P1 wave of the right and left eyes of normal children is not statistically different (P > 0.05). We also found that there is insignificant difference in the visual impact of the colours for both male and female children in terms of reading interest, and red is a more stimulating colour for both sexes.

CONCLUSION: Our study can provide normal reference value and methodological reference for clinical visual acuity detection in children. Combined with the visual characteristics of children, this paper selects the visual impact created by the colour of picture books and combines it with medical treatment. Make the whole test cover the scope of ophthalmology clinical more comprehensive.

PMID:34587563 | DOI:10.1016/j.cmpb.2021.106410

Nanomedicine. 2021 Sep 26:102466. doi: 10.1016/j.nano.2021.102466. Online ahead of print.

ABSTRACT

The purpose of this work was to incorporate an optimized pomegranate extract loaded solid lipid nanoparticles (PE-SLNs) formula in a transdermal emulgel to evaluate its anticancer effect. The prepared emulgel formulae were evaluated for their physicochemical properties. An ex vivo permeation study was done through mouse skin and the kinetic parameters were determined. Kinetic data showed that the ex vivo permeation of PE from SLNs transdermal emulgel through mouse skin followed non-Fickian diffusion transport. Further, in vivo study was done by applying the optimized PE-SLNs transdermal emulgel on mice skin bearing a solid form of Ehrlich ascites carcinoma (EAC) as well as free PE, control, placebo, and standard groups for comparison. In addition, histopathological examinations of the samples obtained from the EAC mice model were performed. The results proved that application of the selected PE-SLNs emulgel formulation on the mice skin bearing solid tumor revealed statistically significant anticancer effects.

PMID:34587542 | DOI:10.1016/j.nano.2021.102466