The efficacy and safety of topical Tretinoin combined with Superficial X‐ray therapy ( SXRT ) in treating Periungual warts

2021 ◽  
Author(s):  
Jinhui Xu ◽  
Deli Zhang ◽  
Lin Feng ◽  
Yang Liu ◽  
Qingchun Diao
Molecules ◽  
2020 ◽  
Vol 25 (8) ◽  
pp. 1910
Author(s):  
U. B. Rao Khandavilli ◽  
Leila Keshavarz ◽  
Eliška Skořepová ◽  
René R. E. Steendam ◽  
Patrick J. Frawley

The presence of impurities can drastically affect the efficacy and safety of pharmaceutical entities. p-Aminophenol (PAP) is one of the main impurities of paracetamol (PA) that can potentially show toxic effects such as maternal toxicity and nephrotoxicity. The removal of PAP from PA is challenging and difficult to achieve through regular crystallization approaches. In this regard, we report four new salts of PAP with salicylic acid (SA), oxalic acid (OX), l-tartaric acid (TA), and (1S)-(+)-10-camphorsulfonic acid (CSA). All the PAP salts were analyzed using single-crystal X-ray diffraction, powder X-ray diffraction, infrared spectroscopy, differential scanning calorimetry, and thermogravimetric analysis. The presence of minute amounts of PAP in paracetamol solids gives a dark color to the product that was difficult to remove through crystallization. In our study, we found that the addition of small quantities of the aforementioned acids helps to remove PAP from PA during the filtration and washings. This shows that salt formation could be used to efficiently remove challenging impurities.


Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 5004-5004
Author(s):  
Silvia Rivas-Vera ◽  
Carlos Cadena-Eumaña ◽  
Juan Chalapud-Revelo ◽  
Adriana Aguilar-Navarro ◽  
Pedro Sobrevilla-Calvo ◽  
...  

Abstract We report the case of a 65 years old woman with a NHL, CD20 +, BCL-2 negative, Grade III, CS: IVBX, FLIPI High Risk, diagnosed on September 2005. The patient was treated with several chemotherapy regimens (CHOP, chlorambucil/prednisone, cyclophosphamide/prednisone), while on treatment a large pleural effusion was found on a chest X-ray. On pleural fluid cytology we observed numerous abnormal lymphocytes. We did repeated thoracocentesis without success, finally a pleural tube was inserted and intrapleural bleomycin instilled, again with no success (Table 1). Six weeks later, after signing informed consent, we administered 50 mg of intrapleural R (50 mg in 50 cc of SS 0.9%) without immediate or delayed adverse events. On day +4 a new chest X-ray showed marked improvement. We planned to repeat the dose every week × 4, unfortunately the patient could not afford it. After seven months the patient is asymptomatic and without recurrence of the pleural effusion. Table 1 Date (2007) Fluid drained (ml) Action September 12 Dyspnea September 21 1,500 October 4 1,500 October 6 570 October 8 400 October 12 20 Bleomycin 10 U November 6 Dyspnea/1,300 November 9 40 November 16 400 November 17 200 November 20 100 Rituximab 50 mg Discussion Although the pharmacology of IV R is welll known, there is scarce information about dosage, penetration into the tissues and efficacy of intracavitary R. It is likely that the intrapleural instillation of R was effective in the control of this complication in a definitive way, without adverse effects, Our case supports the results reported by Schmidt et al (Table 2). The mechanism of action at the local site is not known, but it could be the same as described with the systemic use. Pleural effusion secondary to refractory lymphoma is a rare complication, we propose the integration of an international registry of this cases to study the pharmacokinetics, pharmacodynamics, efficacy and safety of intrapleural rituximab. Table 2 Features Our patient Schmidt Patient Age age 65 years 57 years Diagnosis Follicular NHL, Grado II Lymphoplasmacytic NHL No. Previous Therapy 3 1 Effusion therapy Thoracocentesis and drainage by pleurostomy Thoracocentesis Rituximab Dose 50mg, single dose 50mg day 1 200mg day 2 400mg day 3 Time to Response 4 days 3 days


2011 ◽  
Vol 80 (2) ◽  
pp. 349-356 ◽  
Author(s):  
Hubertus Pietsch ◽  
Gregor Jost ◽  
Thomas Frenzel ◽  
Marian Raschke ◽  
Jakob Walter ◽  
...  

2017 ◽  
pp. 113-123 ◽  
Author(s):  
R. PYTLÍK ◽  
C. RENTSCH ◽  
T. SOUKUP ◽  
L. NOVOTNÝ ◽  
B. RENTSCH ◽  
...  

To evaluate the preclinical efficacy and safety of human mesenchymal stem cells (hMSC) rapidly expanded in growth medium for clinical use with human serum and recombinant growth factors, we conducted a controlled, randomized trial of plasma clots with hMSC vs. plasma clots only in critical segmental femoral defects in rnu/rnu immunodeficient rats. X-ray, microCT and histomorphometrical evaluation were performed at 8 and 16 weeks. MSC were obtained from healthy volunteers and patients with lymphoid malignancy. Human MSC survived in the defect for the entire duration of the trial. MSC from healthy volunteers, in contrast to hMSC from cancer patients, significantly improved bone healing at 8, but not 16 weeks. However, at 16 weeks, hMSC significantly improved vasculogenesis in residual defect. We conclude that hMSC from healthy donors significantly contributed to the healing of bone defects at 8 weeks and to the vascularisation of residual connective tissue for up to 16 weeks. We found the administration of hMSC to be safe, as no adverse reaction to human cells at the site of implantation and no evidence of migration of hMSC to distant organs was detected.


2019 ◽  
Vol 45 (10) ◽  
pp. 1245-1252 ◽  
Author(s):  
Tian Tian ◽  
Yao-Jia Luo ◽  
Hua Wang ◽  
Hong-Duo Chen ◽  
Yuan-Hong Li

2021 ◽  
Author(s):  
Adam Peter Skidmore

Abstract Background Chronic strictures following Roux en Y Gastric Bypass (RYGB) are a troublesome complication that can lead to significant morbidity. The use of stents has been described but the need for X-ray and risk of migration have meant limited use in the management of these strictures. Lumen apposing metal stents (LAMS) have traditionally been used for management of pancreatic pseudocysts. They don’t require X-ray and are easy to deploy with a short learning curve. This paper explores the use of LAMS to treat post RYGB strictures and explores their safety and efficacy.MethodsA prospective study over a 4-year period looking at 14 patients with post RYGB strictures. These patients have been followed up for between 1 and 3 years. We have prospectively collected data on the efficacy and safety of LAMS in these patientsResults421 patients underwent RYGB in the study period. 14 of these patients developed a stricture that resulted in insertion of LAMS. There was no immediate complications and 12 patients had complete resolution of their stricture. There were no migration related issues.ConclusionLAMS are a safe and effective method to manage post RYGB strictures. They have a high rate of resolution of strictures and can be safely deployed across strictures with no immediate complication. Migration does not appear to be a problem. Insertion is straightforward and doesn’t appear to be associated with a long learning curve.


2021 ◽  
Author(s):  
Wang Wenyue ◽  
Xu Yingpeng ◽  
Ding Quanmao ◽  
Xie Li-min ◽  
Wang De-zhi ◽  
...  

Abstract Background: Both massage and topically administered NSAIDs are safe and effective treatment for knee osteoarthritis (KOA); however, different massage technique sects in China caused assessment difficulties for the treatment of KOA. In order to standardize massage techniques and procedures, we organized multi-disciplinary experts in China to acquire an evidence-based traditional Chinese medicine massage treatment of knee osteoarthritis. The purposes of this study are to evaluate the efficacy and safety of evidence-based traditional Chinese medicine massage treatment of KOA compared to External Diclofenac Diethylamine Emulgel.Methods and design: 300 participants diagnosed with KOA will be randomly divided into the experimental group, control group, and waiting list group in a ratio of 2:1. The participants will receive evidence-based traditional Chinese medicine massage 2 sessions per week for 10 weeks or External Diclofenac Diethylamine Emulgel 3-4 times per day for 10 weeks respectively. The MRI scans and X-ray will be performed at baseline and the end of the intervention period. The main evaluation index will include the Western Ontario and McMaster Osteoarthritis Index (WOMAC). The secondary evaluation index will include:(1) WOMAC each dimension; (2) the PRO scale for knee osteoarthritis based on the concept of Traditional Chinese Medicine(Chinese scale for knee osteoarthritis, CSKO); (3) MRI scan and X-ray evaluation.Discussion: The results of our study will help to evaluate efficacy and safety of evidence-based traditional Chinese medicine massage treatment of KOA compared with External Diclofenac Diethylamine Emulgel combined with clinical, X-ray and MRI changes. Trial registration: Chinese Clinical Trial Registry ChiCTR1800014400. Registered on 10 January 2018.


2011 ◽  
pp. 93-100
Author(s):  
Ngoc Doanh Pham ◽  
Thi Kim Quy Tran

Background: Ingested foreign things in peptogaster are acute cases that are frequently seen in clinical practices. Flexible endoscopic removal of the ingested foreign things is now the first choice. Aims: Investigating characsteristics of ingested foreign things, and evaluating the efficacy and safety of endoscopic removal techniques. Subjects and Methods: 47 patients participated in the study. Diagnosis of ingested foreign things have made by history, clinical manifestations, X – ray and endoscopy????. The used instruments are conventional flexible endoscopy and assessories???. Results and Discussion: The ingested foreign things are duck bones 31,9%, fish bones 29.8%, chicken bones 12.8%, dental prostheses 12.8%, pig bones 10.6% and bamboo sticks 2.1%. Endoscopic removal have been successfully performed making up 93.6%.There were some minor complications such as bleeding erosions (4.4%), no case with serious complications. Conclusion: Flexible endoscopic removal is an effective and relatively safe procedure for patients with digested foreign things.


2021 ◽  
Author(s):  
Kulthanit Wanaratna ◽  
Pornvimol Leethong ◽  
Nitapha Inchai ◽  
Wararath Chueawiang ◽  
Pantitra Sriraksa ◽  
...  

Objective: To assess the efficacy and safety of Andrographis paniculata extract (APE) in adults with mild COVID-19. Methods: The alcoholic extract of the aerial part of A. paniculata was used. In this randomized, double-blinded, placebo-controlled trial, adults with laboratory-confirmed COVID-19, and mild symptoms were randomized 1:1 to receive APE (60 mg andrographolide, t.i.d, for 5 days) versus placebo, plus standard supportive care. Blood tests for CRP, liver and renal assessment were performed on Days 1, 3, and 5. The outcomes were occurrence of pneumonia detected by chest X-ray, nasopharyngeal SARS-CoV-2 detection by rRT-PCR, changes of CRP levels, and adverse drug reactions. Results: Patients were randomized to receive APE (n=29) or placebo (n=28). Pneumonia occurrence during illness was 0/29 (0%) versus 3/28 (10.7%), (p=0.039); and patients with nasopharyngeal SARS-CoV-2 detection on Day 5 were 10/29 (34.5%) versus 16/28 (57.1%), (p=0.086), for those who received APE and placebo, respectively. All three patients with pneumonia had substantially rising serum CRP; and high CRP levels on Day 5. None had evidence of liver or renal impairment. Conclusion: This AP-extract treatment regimen was potentially effective and safe in adults with mild COVID-19. The rising of CRP suggested disease progression. Further studies are needed.


2021 ◽  
Author(s):  
Eric Lattmann ◽  
Pradnya Bhalerao ◽  
BL ShashiBhushan ◽  
Neeta Nargundkar ◽  
Pornthip Lattmann ◽  
...  

ABSTARCTObjectiveTo evaluate the efficacy and safety of PNB001 a CCK-A agonist and CCK-B antagonist, a new chemical entity with anti-inflammatory and immune stimulation properties, along with Standard of Care (SOC) in patients with moderate COVID-19 infection.DesignMulti-center, randomized, parallel group, comparative, open label study.SettingTwo tertiary-care hospitals in India.ParticipantsPatients with laboratory-confirmed SARS-CoV-2 infection as determined by polymerase chain reaction (PCR) within 2 days of randomization, having pneumonia with no signs of severe disease (severe disease means SpO2≤94% on room air), and any two of the following signs or symptoms suggestive of COVID-19: fever, cough, dyspnea, or hypoxia.InterventionsPatients were randomized 1:1 to receive PNB001 at an oral dose of 100 mg three times daily for 14 days with Standard of Care (PNB001+SOC) or only SOC.Main outcome measuresThe primary endpoints were mean change in the 8-point WHO Ordinal Scale score from baseline by Day 14 and mortality rate by Day 28. The key secondary endpoints were percentage of patients showing change in clinical status using the ordinal scale, improvement in inflammatory segments in X-ray chest, reduction of days of hospitalization, duration of supplemental oxygen use, days to negative PCR for COVID-19 and change in inflammation markers Interlukin-6 (IL6) and C-reactive protein (CRP) from baseline by Day 14.ResultsA total of 40 (20 in PNB 001+SOC arm and 20 in SOC arm) patients were randomized and received treatment. The primary endpoint showed significant clinical improvement from baseline to Day 14 with PNB001+SOC (0.22 Vs 1.12; P=0.0421). One patient in PNB001+SOC arm and two patients in SOC arm died (1 Vs 2; HR: 2.0 [95%CI=0.18, 22.05]; P=0.5637) by Day 28. At the end of the treatment by Day 14, more patients achieved zero ordinal scale in PNB001+SOC arm (17 Vs 12; P=0.0766). In the PNB001+SOC arm, change in mean chest X-ray score showed significant improvement (2.05 Vs 1.16; P=0.0321), and more patients quickly showed complete improvement (10 Vs 7; HR: 1.48 [95%CI=0.64, 3.44]; P=0.4309). In the PNB001+SOC arm, patients needed shorter duration of hospitalization in days (9.45 Vs 9.80) and more patients attained earlier discharge from the hospital (19 Vs 15; P=0.0486) with respect to days. The mean duration of supplemental oxygen requirement in days was shorter (5.45 Vs 7.10) and complete withdrawal from supplemental oxygen was more frequent with PNB001+SOC compared to SOC by Day 14 (17 Vs 13; P=0.1441). All patients in both the arms had negative PCR by the end of the study (18 Vs 17; P=0.6265) by similar time (7.6 Vs 7.0). Exploratory analysis done for IL-6, CRP, Neutrophil-Lymphocyte-Ratio (NLR), Platelet-Lymphocyte-Ratio (PLR) and Erythrocyte Sedimentation Rate (ESR) showed statistically significant reduction by Day 14 demonstrating PNB001’s anti-inflammatory and immunomodulatory properties. Lymphocyte and neutrophil counts also improved by Day 14. 11 adverse events (AE) in 8 patients were observed with PNB001+SOC compared to 13 AEs in 10 patients with SOC; none of the AEs in PNB001+SOC arm were related to PNB001. The most common AE were tachycardia and acute respiratory distress syndrome; there were isolated cases of hepatic enzyme elevation and hyperglycemia. Overall, safety profile was similar between PNB001+SOC and SOC arms.ConclusionsPNB001 with standard of care showed significant clinical improvement in moderate COVID-19 patients when compared to standard of care and was well tolerated by moderate COVID-19 patients.Trial RegistrationCTRI/2020/10/028423


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