journal
https://read.qxmd.com/read/38493002/association-between-first-time-neurologic-events-and-metronidazole-treatment-a-case-time-control-study
#21
JOURNAL ARTICLE
Michael Asger Andersen, Rasmus Gregersen, Tonny Studsgaard Petersen, Joanna Nan Wang, Janne Petersen, Espen Jimenez-Solem
PURPOSE: Metronidazole, a widely used antimicrobial medication, has been linked to neurologic adverse drug reactions. This study investigates the association between metronidazole use and first-time neurologic events. METHODS: We conducted a case-time-control study using data from the Danish National Patient Register and the National Prescription Register in years 2013 to 2021. Patients with a first-time diagnosis of encephalopathy, cerebellar dysfunction, or peripheral neuropathy were included...
March 15, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38485588/advanced-model-based-approach-to-evaluate-human-plasma-cerebrospinal-fluid-and-neuronal-mtorc1-activation-biomarkers-after-nv-5138-administration-in-healthy-volunteers
#22
JOURNAL ARTICLE
Azmi Nasser, J Randall Owen, Roberto Gomeni, Alisa R Kosheleff, Jeanelle Portelli, Lilian W Adeojo, Thomas E Hughes
PURPOSE: NV-5138 ([S]-2-amino-5,5-difluoro-4,4-dimethylpentanoic acid) is an orally bioavailable, small-molecule activator of the mechanistic target of rapamycin complex 1 (mTORC1) pathway in development for treatment-resistant depression. The authors established a model to describe the relationship between plasma and cerebrospinal fluid (CSF) concentrations of NV-5138 and between CSF concentrations and potential biomarkers thought to be associated with mTORC1 activity (ie, orotic acid, N-acetylmethionine, and N-formylmethionine)...
March 13, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38462427/thiazolidinediones-are-partially-effective-bitter-blockers
#23
JOURNAL ARTICLE
Ha Nguyen, Cailu Lin, Ivona Sasimovich, Katherine Bell, Amy Huang, Emilia Leszkowicz, Nancy E Rawson, Danielle R Reed
PURPOSE: The bad bitter taste of some medicines is a barrier to overcoming noncompliance with medication use, especially life-saving drugs given to children and the elderly. Here, we evaluated a new class of bitter blockers (thiazolidinediones, TZDs). METHODS: In this study, 2 TZDs were tested, rosiglitazone (ROSI) and a simpler form of TZD, using a high-potency sweetener as a positive control (neohesperidin dihydrochalcone, NHDC). We tested bitter-blocking effects using the bitter drugs tenofovir alafenamide fumarate (TAF), a treatment for HIV and hepatitis B infection, and praziquantel (PRAZ), a treatment for schistosomiasis, by conducting taste testing with 2 separate taste panels: a general panel (N = 97, 20-23 years, 82...
March 9, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38461122/global-risdiplam-compassionate-use-program-for-patients-with-type-1-or-2-spinal-muscular-atrophy
#24
JOURNAL ARTICLE
Rakesh Kantaria, Karen Baker, Senam Beckley-Kartey, Ksenija Gorni, Isabelle Montrocher-Ober, Laurence Vindevoghel
PURPOSE: Spinal muscular atrophy (SMA) is a genetic neuromuscular disease causing progressive muscle weakness and reducing life expectancy. Risdiplam (Evrysdi; Genentech/F. Hoffmann-La Roche Ltd, Basel, Switzerland) is a drug approved for use in the treatment of patients with SMA. The ongoing global risdiplam Compassionate Use Program (CUP), initiated in November 2019, is the largest CUP in SMA, currently providing access to risdiplam for >2000 patients with type 1 or 2 SMA in 59 countries...
March 8, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38458901/nirmatrelvir-and-ritonavir
#25
EDITORIAL
Paul Beninger
No abstract text is available yet for this article.
March 7, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38429119/attainment-of-target-in-therapeutic-range-of-international-normalized-ratio-and-correlates-among-patients-on-warfarin-therapy-at-jimma-medical-center-jimma-ethiopia
#26
JOURNAL ARTICLE
Abdulkadir Urgessa Jada, Gashahun Mekonnen Disassa, Belete Habte Melesse, Mohammed Mecha Abafogi, Eyob Girma Abera, Kelil Hussein Jibicho, Kedir Negesso Tukeni
PURPOSE: Warfarin is effective therapy to prevent thromboembolic complications of venous thromboembolism, atrial fibrillation, and cardiac thrombus, among valvular heart diseases, including in patients treated with prostheses and/or repair. Its optimum effect is achieved when the international normalized ratio (INR) is in the target therapeutic range, but a subtherapeutic level increases risk of thromboembolism and complications. This study aimed to assess the attainment of target therapeutic range, proportion, and factors associated with subtherapeutic level of warfarin...
February 29, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38403509/comparison-of-empiric-antibiotic-treatment-regimens-for-hospitalized-non-severe-community-acquired-pneumonia-a-retrospective-multicenter-cohort-study
#27
JOURNAL ARTICLE
Sidney D Reeves, Aaron P Hartmann, Amanda C Tedder, Paul A Juang, Mikaela Hofer, Marin H Kollef, Scott T Micek, Kevin D Betthauser
PURPOSE: Consensus guidelines for hospitalized, non-severe community-acquired pneumonia (CAP) recommend empiric macrolide + β-lactam or respiratory fluoroquinolone monotherapy in patients with no risk factors for resistant organisms. In patients with allergies or contraindications, doxycycline + β-lactam is a recommended alternative. The purpose of this study was to compare differences in outcomes among guideline-recommended regimens in this population. METHODS: This retrospective, multicenter cohort study included patients ≥18 years of age with CAP who received respiratory fluoroquinolone monotherapy, empiric macrolide + β-lactam, or doxycycline + β-lactam...
February 24, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38403508/effectiveness-tolerability-and-safety-of-different-amphotericin-b-formulations-in-invasive-fungal-infections-a-multicenter-retrospective-observational-study
#28
JOURNAL ARTICLE
Francelise Bridi Cavassin, Marcello Mihailenko Chaves Magri, Jose Ernesto Vidal, Fabianne Altruda de Moraes Costa Carlesse, Diego Rodrigues Falci, João Luís Baú-Carneiro, Giovanni Luís Breda, Fábio de Araújo Motta, Cássia Silva de Miranda Godoy, Renata de Bastos Ascenço Soares, Carla Sakuma De Oliveira, Ana Verena Almeida Mendes, Hugo Paz Morales, Patrícia Silva Montes, Mariane Taborda, Caroline Martins Rego, Maíra Araujo Félix, Paula Pacheco Katopodis, Julia Raquel da Silva do Ó, Mirela Pereira Lima Abrão, Talita Teles Teixeira Pereira, Flávio Queiroz-Telles
PURPOSE: Data on the real-life use of amphotericin B lipid complex (ABLC) compared with other available formulations are limited. This study aimed to evaluate the effectiveness, tolerability, and safety of different amphotericin B (AMB) intravenously administered in the context of hospital practice for the treatment of invasive fungal infections (IFI) and to provide new insights into the profile of ABLC. METHODS: This is a multicenter, retrospective, observational study conducted at 10 tertiary Brazilian hospitals...
February 24, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38369451/physiologically-based-pharmacokinetic-modeling-of-lacosamide-in-patients-with-hepatic-and-renal-impairment-and-pediatric-populations-to-support-pediatric-dosing-optimization
#29
JOURNAL ARTICLE
Xinyu Zhu, Lingfeng Guo, Lei Zhang, Yichao Xu
PURPOSE: Lacosamide (LCM) is a new-generation anti-seizure medication that is efficacious in patients with focal seizures with or without secondary generalization. Until now, the efficacy, safety, and tolerability of LCM are still lacking in Chinese epilepsy patients, particularly for pediatric populations and patients with renal or hepatic impairment. METHODS: This study was conducted to develop a physiologically based pharmacokinetic (PBPK) model to characterize the pharmacokinetics of LCM in Chinese populations and predict the pharmacokinetics of LCM in Chinese pediatric populations and patients with renal or hepatic impairment...
February 17, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38368167/effect-of-optimizing-the-induction-regimen-in-preventing-cough-reactions-in-patients-undergoing-general-anesthesia-a-prospective-randomized-controlled-study
#30
JOURNAL ARTICLE
Lei Wang, Xing Lu, Yi Cheng, You-Chuan Zhang, De-Xiang Zhao, Yan-Hong Zhu
PURPOSE: During the induction of general anesthesia, opioids and endotracheal intubation may cause coughing. This study aimed to investigate the safety and effectiveness of an optimized drug induction scheme for general anesthesia to prevent coughing in patients. METHODS: A total of 220 patients aged 18 to 65 years who underwent surgery under general anesthesia with endotracheal intubation were randomly assigned to two groups, each with 110 patients. One group was administered a divided sufentanil bolus (group A) and the other with a single sufentanil bolus (group B)...
February 16, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38360447/therapeutic-effect-and-side-effects-of-pharmacotherapy-in-patients-with-parkinson-disease-and-myasthenia-gravis-a-systematic-review-of-case-reports-and-case-series-studies
#31
REVIEW
Haoyu Xie, Yadi Liu, Cindy Schmidt, Jung Hung Chien, Chuhuai Wang
PURPOSE: The co-existence of Parkinson disease (PD) and myasthenia gravis (MG) in an individual should be exceptionally rare. The purpose of this study was to systematically review the current literature regarding the therapeutic effect and side effects of pharmacotherapy on patients with PD and MG. METHODS: Five bioscience and engineering databases (MEDLINE via PubMed, Cochrane Library, Scopus, EMBASE, and China National Knowledge Infrastructure) were searched from inception through February 21, 2022...
February 14, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38350757/effect-of-household-income-on-cardiovascular-diseases-cardiovascular-biomarkers-and-socioeconomic-factors
#32
JOURNAL ARTICLE
Mengjin Hu, Boyu Li, Tao Yang, Yuejin Yang, Chunlin Yin
PURPOSE: To examine whether household income is causally related to cardiovascular diseases and investigate the potential reasons. METHODS: Using 2-sample Mendelian randomization analyses, we obtained summary statistics from genome-wide association studies of household income and a range of cardiovascular diseases, biomarkers, and socioeconomic factors. FINDINGS: Higher household income was causally associated with lower risks of coronary heart disease (odd ratio [OR] = 0...
February 12, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38350756/efficacy-of-sevoflurane-and-propofol-anesthesia-on-perioperative-adverse-cardiovascular-events-and-hemodynamics-in-elderly-patients-with-diabetes
#33
JOURNAL ARTICLE
Liling Jia, Hongfeng Li, Tuping Li
PURPOSE: This study was undertaken to compare the effects of sevoflurane and propofol anesthesia on perioperative hemodynamics and perioperative adverse cardiovascular events (PACE) in elderly patients with diabetes undergoing general anesthesia for noncardiac surgery. METHODS: According to the random number table (n = 40), 80 patients with diabetes undergoing noncardiac general anesthesia were divided into a control group and an observation group. In the control group, the patients were given propofol 4 to 6 mg/(kg·h), continuously pumped to maintain anesthesia...
February 12, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38342708/phase-i-studies-innovations-and-issues
#34
JOURNAL ARTICLE
Paul Beninger
INTRODUCTION: Emeritus Editor-in-Chief, Richard Shader, published 2 editorials in 2014 to state that Clinical Therapeutics' would no longer consider simple innovator vs generic bioequivalence studies for publication and would require a rationale for the choice of agents when submitting drug-drug interaction studies for consideration. The intervening decade of developments in this field provides an opportunity to comment on these trends. Lewis Scheiner anchors the subsequent discussion in a "Learn and Confirm" super-structure of thinking about the goals of early development of pharmaceutical agents...
February 10, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38423866/a-relative-bioavailability-bioequivalence-and-food-effect-study-of-niraparib-tablets-in-patients-with-advanced-solid-tumors
#35
RANDOMIZED CONTROLLED TRIAL
Gerald Falchook, Amita Patnaik, Debra L Richardson, R Donald Harvey, Manish R Sharma, Navid Hafez, Erika Hamilton, Sarina A Piha-Paul, Minal Barve, Trisha Wise-Draper, Manish R Patel, Afshin Dowlati, Joseph Pascuzzo, Shou-Ching Tang, Christina Faltermeier, Izabela A Malinowska, Luda Shtessel, Alina Striha, Elizabeth Potocka
PURPOSE: The poly (ADP-ribose) polymerase inhibitor niraparib is indicated as maintenance treatment in patients with certain subtypes of advanced ovarian cancer, and is being investigated in patients with other solid tumors. Niraparib is available in 100-mg capsules with a starting dosage of 200 or 300 mg/d. This study assessed the relative bioavailability (BA) and bioequivalence (BE) between a 1 × 300-mg tablet relative to 3 × 100-mg niraparib capsules. In addition, the food effect (FE) of a high-fat meal on the pharmacokinetic (PK) properties of tablet-formulated niraparib was investigated...
March 2024: Clinical Therapeutics
https://read.qxmd.com/read/38326158/lenacapavir
#36
EDITORIAL
Paul Beninger
No abstract text is available yet for this article.
February 6, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38310052/use-of-dulaglutide-semaglutide-and-tirzepatide-in-diabetes-and-weight-management
#37
JOURNAL ARTICLE
Jason Powell, James Taylor
PURPOSE: Glucagon-like peptide 1 receptor agonists (GLP1-RA) are effective therapies in lowering glycosylated hemoglobin (HbA1c ), providing cardioprotective benefits, and lowering weight. The use of GLP1-RA solely for weight-loss has become commonplace in many practices, which in turn has made it difficult in some areas for those with type 2 diabetes (T2DM) to obtain these much-needed medications. METHODS: Using recent published literature, along with clinical experience, it has become apparent that many GLP1-RAs have become difficult to obtain for patients with diabetes...
February 2, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38307725/the-safety-and-efficacy-of-abaloparatide-on-postmenopausal-osteoporosis-a-systematic-review-and-meta-analysis
#38
JOURNAL ARTICLE
Fuxin Xu, Yurun Wang, Xinjian Zhu
PURPOSE: The aging of the population increases the incidence of postmenopausal osteoporosis, which threatens the health of elderly women. Abaloparatide is a synthetic peptide analogue of the human parathyroid hormone-related protein that has recently been approved for the treatment of postmenopausal osteoporosis. Its efficacy and safety have not been systematically evaluated. Therefore, studies on the efficacy and safety of abaloparatide could be of assistance in the clinical medication of postmenopausal osteoporosis...
February 1, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38307724/a-physiologically-based-pharmacokinetic-modeling-approach-to-assess-the-potential-for-drug-interactions-between-trofinetide-and-cyp3a4-metabolized-drugs
#39
JOURNAL ARTICLE
Mona Darwish, James M Youakim, Inger Darling, Viera Lukacova, Joel S Owen, Heather Bradley
PURPOSE: Trofinetide is the first drug to be approved by the US Food and Drug Administration for use in the treatment of patients with Rett syndrome, a multisystem disorder requiring multimodal therapies. Cytochrome P450 (CYP) 3A4 metabolizes >50% of therapeutic drugs and is the CYP isozyme most commonly expressed in the liver and intestines. In vitro studies suggest the concentration of trofinetide producing 50% inhibition (IC50 ) of CYP3A4 is >15 mmol/L; that concentration was much greater than the target clinical concentration associated with the maximal intended therapeutic dose (12 g)...
February 1, 2024: Clinical Therapeutics
https://read.qxmd.com/read/38216351/efficacy-and-safety-of-csf-1-0-4-pilocarpine-hydrochloride-in-presbyopia-pooled-results-of-the-near-phase-3-randomized-clinical-trials
#40
RANDOMIZED CONTROLLED TRIAL
Edward Holland, Paul Karpecki, Murray Fingeret, Jack Schaeffer, Preeya Gupta, Nicole Fram, Gerard Smits, Teresa Ignacio, Richard Lindstrom
PURPOSE: This study was undertaken to evaluate the safety and efficacy of CSF-1 (0.4% pilocarpine hydrochloride ophthalmic solution) for use in individuals with presbyopia. METHODS: Two Phase 3 multicenter, randomized, double-masked, vehicle-controlled, parallel-group clinical trials were conducted in 35 private ophthalmology clinics in the United States from October 2020 to February 2022. Key inclusion criteria were the following: (1) age 45-64 years, (2) distance-corrected near visual acuity (DCNVA) at 40 cm ≥0...
February 2024: Clinical Therapeutics
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