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  1. Book ; Thesis: Recurrent streptococcal pharyngotonsillitis

    Orrling, Arne

    studies on etiology and treatment

    (Doctoral dissertation series; 2006,32 ; 2006,32)

    2006  

    Author's details Arne Orrling
    Series title Doctoral dissertation series; 2006,32 ; 2006,32
    Doctoral dissertation series
    Doctoral dissertation series; 2006,32
    Collection Doctoral dissertation series
    Doctoral dissertation series; 2006,32
    Language English ; Swedish
    Size Getr. Zählung : Ill., graph. Darst.
    Publishing country Sweden
    Document type Book ; Thesis
    Thesis / German Habilitation thesis Lund, Univ., Diss., 2006
    Note Zsfassung in schwed. Sprache
    HBZ-ID HT014724925
    ISBN 91-85481-57-2 ; 978-91-85481-57-6
    Database Catalogue ZB MED Medicine, Health

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  2. Article ; Online: Simultaneous determination of folate and methotrexate metabolites in serum by LC-MS/MS during high-dose methotrexate therapy.

    Hansson, Karin / Orrling, Henrik / Blomgren, Anders / Isaksson, Anders / Schliamser, Gloria / Heldrup, Jesper / Pronk, Cornelis Jan

    Journal of chromatography. B, Analytical technologies in the biomedical and life sciences

    2021  Volume 1186, Page(s) 123007

    Abstract: High-dose methotrexate (HDMTX) is a central component in the treatment of acute lymphoblastic leukemia, osteosarcoma, and some lymphomas and brain tumors. MTX is given at lethal doses and then is followed by rescue treatment with folinic acid (FA). ... ...

    Abstract High-dose methotrexate (HDMTX) is a central component in the treatment of acute lymphoblastic leukemia, osteosarcoma, and some lymphomas and brain tumors. MTX is given at lethal doses and then is followed by rescue treatment with folinic acid (FA). Despite FA rescue, many patients suffer severe toxicity. The pharmacokinetics of FA rescue have not been sufficiently studied. However, optimization of FA rescue could potentially increase anti-tumor effects, whilst decreasing organ toxicity. Here, we describe our efforts to establish and optimize a liquid chromatography tandem mass spectrometric (LC-MS/MS) method for the simultaneous determination of five essential components of the folate cycle, as well as MTX and its two metabolites. The method was applied to 6 individual patients receiving HDMTX, with 3 or 4 measurements for each patient. The method allows analysis of samples that were initially frozen. This notion, together with the test results in the 6 pilot patients, shows the feasibility of this method to study MTX and FA pharmacokinetics during HDMTX treatment. The method has the potential to optimize HDMTX and FA rescue treatment in individual patients.
    MeSH term(s) Antineoplastic Agents/administration & dosage ; Antineoplastic Agents/blood ; Chromatography, Liquid/methods ; Dose-Response Relationship, Drug ; Folic Acid/administration & dosage ; Folic Acid/blood ; Humans ; Methotrexate/administration & dosage ; Methotrexate/blood ; Pilot Projects ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/blood ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy ; Tandem Mass Spectrometry/methods
    Chemical Substances Antineoplastic Agents ; Folic Acid (935E97BOY8) ; Methotrexate (YL5FZ2Y5U1)
    Language English
    Publishing date 2021-11-10
    Publishing country Netherlands
    Document type Evaluation Study ; Journal Article
    ZDB-ID 1180823-8
    ISSN 1873-376X ; 0378-4347 ; 1570-0232 ; 1387-2273
    ISSN (online) 1873-376X
    ISSN 0378-4347 ; 1570-0232 ; 1387-2273
    DOI 10.1016/j.jchromb.2021.123007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Pharyngotonsillitis.

    Stjernquist-Desatnik, Anna / Orrling, Arne

    Periodontology 2000

    2009  Volume 49, Page(s) 140–150

    MeSH term(s) Adolescent ; Anti-Bacterial Agents/therapeutic use ; Child ; Child, Preschool ; Humans ; Pharyngitis/drug therapy ; Pharyngitis/microbiology ; Pharyngitis/virology ; Streptococcal Infections/drug therapy ; Streptococcal Infections/microbiology ; Streptococcus/pathogenicity ; Tonsillitis/drug therapy ; Tonsillitis/microbiology ; Tonsillitis/virology ; Virulence Factors
    Chemical Substances Anti-Bacterial Agents ; Virulence Factors
    Keywords covid19
    Language English
    Publishing date 2009-01-19
    Publishing country Denmark
    Document type Journal Article ; Review
    ZDB-ID 1200504-6
    ISSN 1600-0757 ; 0906-6713
    ISSN (online) 1600-0757
    ISSN 0906-6713
    DOI 10.1111/j.1600-0757.2008.00282.x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: The European Lead Factory: A Blueprint for Public-Private Partnerships in Early Drug Discovery.

    Karawajczyk, Anna / Orrling, Kristina M / de Vlieger, Jon S B / Rijnders, Ton / Tzalis, Dimitrios

    Frontiers in medicine

    2017  Volume 3, Page(s) 75

    Abstract: The European Lead Factory (ELF) is a public-private partnership (PPP) that provides researchers in Europe with a unique platform for translation of innovative biology and chemistry into high-quality starting points for drug discovery. It combines an ... ...

    Abstract The European Lead Factory (ELF) is a public-private partnership (PPP) that provides researchers in Europe with a unique platform for translation of innovative biology and chemistry into high-quality starting points for drug discovery. It combines an exceptional collection of small molecules, high-throughput screening (HTS) infrastructure, and hit follow-up capabilities to advance research projects from both private companies and publicly funded researchers. By active interactions with the wider European life science community, ELF connects and unites bright ideas, talent, and experience from several disciplines. As a result, ELF is a unique, collaborative lead generation engine that has so far resulted in >4,500 hit compounds with a defined biological activity from 83 successfully completed HTS and hit evaluation campaigns. The PPP has also produced more than 120,000 novel innovative library compounds that complement the 327,000 compounds contributed by the participating pharmaceutical companies. Intrinsic to its setup, ELF enables breakthroughs in areas with unmet medical and societal needs, where no individual entity would be able to create a comparable impact in such a short time.
    Language English
    Publishing date 2017-01-19
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2775999-4
    ISSN 2296-858X
    ISSN 2296-858X
    DOI 10.3389/fmed.2016.00075
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Safety and Tolerability of Online Adaptive High-Field Magnetic Resonance-Guided Radiotherapy.

    Westerhoff, Jasmijn M / Daamen, Lois A / Christodouleas, John P / Blezer, Erwin L A / Choudhury, Ananya / Westley, Rosalyne L / Erickson, Beth A / Fuller, Clifton D / Hafeez, Shaista / van der Heide, Uulke A / Intven, Martijn P W / Kirby, Anna M / Lalondrelle, Susan / Minsky, Bruce D / Mook, Stella / Nowee, Marlies E / Marijnen, Corrie A M / Orrling, Kristina M / Sahgal, Arjun /
    Schultz, Christopher J / Faivre-Finn, Corinne / Tersteeg, Robbert J H A / Tree, Alison C / Tseng, Chia-Lin / Schytte, Tine / Silk, Dustin M / Eggert, Dave / Luzzara, Marco / van der Voort van Zyp, Jochem R N / Verkooijen, Helena M / Hall, William A

    JAMA network open

    2024  Volume 7, Issue 5, Page(s) e2410819

    Abstract: Importance: In 2018, the first online adaptive magnetic resonance (MR)-guided radiotherapy (MRgRT) system using a 1.5-T MR-equipped linear accelerator (1.5-T MR-Linac) was clinically introduced. This system enables online adaptive radiotherapy, in which ...

    Abstract Importance: In 2018, the first online adaptive magnetic resonance (MR)-guided radiotherapy (MRgRT) system using a 1.5-T MR-equipped linear accelerator (1.5-T MR-Linac) was clinically introduced. This system enables online adaptive radiotherapy, in which the radiation plan is adapted to size and shape changes of targets at each treatment session based on daily MR-visualized anatomy.
    Objective: To evaluate safety, tolerability, and technical feasibility of treatment with a 1.5-T MR-Linac, specifically focusing on the subset of patients treated with an online adaptive strategy (ie, the adapt-to-shape [ATS] approach).
    Design, setting, and participants: This cohort study included adults with solid tumors treated with a 1.5-T MR-Linac enrolled in Multi Outcome Evaluation for Radiation Therapy Using the MR-Linac (MOMENTUM), a large prospective international study of MRgRT between February 2019 and October 2021. Included were adults with solid tumors treated with a 1.5-T MR-Linac. Data were collected in Canada, Denmark, The Netherlands, United Kingdom, and the US. Data were analyzed in August 2023.
    Exposure: All patients underwent MRgRT using a 1.5-T MR-Linac. Radiation prescriptions were consistent with institutional standards of care.
    Main outcomes and measures: Patterns of care, tolerability, and technical feasibility (ie, treatment completed as planned). Acute high-grade radiotherapy-related toxic effects (ie, grade 3 or higher toxic effects according to Common Terminology Criteria for Adverse Events version 5.0) occurring within the first 3 months after treatment delivery.
    Results: In total, 1793 treatment courses (1772 patients) were included (median patient age, 69 years [range, 22-91 years]; 1384 male [77.2%]). Among 41 different treatment sites, common sites were prostate (745 [41.6%]), metastatic lymph nodes (233 [13.0%]), and brain (189 [10.5%]). ATS was used in 1050 courses (58.6%). MRgRT was completed as planned in 1720 treatment courses (95.9%). Patient withdrawal caused 5 patients (0.3%) to discontinue treatment. The incidence of radiotherapy-related grade 3 toxic effects was 1.4% (95% CI, 0.9%-2.0%) in the entire cohort and 0.4% (95% CI, 0.1%-1.0%) in the subset of patients treated with ATS. There were no radiotherapy-related grade 4 or 5 toxic effects.
    Conclusions and relevance: In this cohort study of patients treated on a 1.5-T MR-Linac, radiotherapy was safe and well tolerated. Online adaptation of the radiation plan at each treatment session to account for anatomic variations was associated with a low risk of acute grade 3 toxic effects.
    MeSH term(s) Humans ; Radiotherapy, Image-Guided/methods ; Radiotherapy, Image-Guided/adverse effects ; Male ; Female ; Middle Aged ; Aged ; Neoplasms/radiotherapy ; Neoplasms/diagnostic imaging ; Adult ; Prospective Studies ; Magnetic Resonance Imaging/methods ; Feasibility Studies ; Cohort Studies ; Aged, 80 and over
    Language English
    Publishing date 2024-05-01
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2574-3805
    ISSN (online) 2574-3805
    DOI 10.1001/jamanetworkopen.2024.10819
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Identification of Phenylpyrazolone Dimers as a New Class of Anti-Trypanosoma cruzi Agents.

    Sijm, Maarten / Siciliano de Araújo, Julianna / Ramos Llorca, Alba / Orrling, Kristina / Stiny, Lydia / Matheeussen, An / Maes, Louis / de Esch, Iwan J P / de Nazaré Correia Soeiro, Maria / Sterk, Geert Jan / Leurs, Rob

    ChemMedChem

    2019  Volume 14, Issue 18, Page(s) 1662–1668

    Abstract: Chagas disease is becoming a worldwide problem; it is currently estimated that over six million people are infected. The two drugs in current use, benznidazole and nifurtimox, require long treatment regimens, show limited efficacy in the chronic phase of ...

    Abstract Chagas disease is becoming a worldwide problem; it is currently estimated that over six million people are infected. The two drugs in current use, benznidazole and nifurtimox, require long treatment regimens, show limited efficacy in the chronic phase of infection, and are known to cause adverse effects. Phenotypic screening of an in-house library led to the identification of 2,2'-methylenebis(5-(4-bromophenyl)-4,4-dimethyl-2,4-dihydro-3H-pyrazol-3-one), a phenyldihydropyrazolone dimer, which shows an in vitro pIC
    MeSH term(s) Animals ; Cells, Cultured ; Dimerization ; Dose-Response Relationship, Drug ; Humans ; Mice ; Molecular Structure ; Parasitic Sensitivity Tests ; Pyrazolones/chemical synthesis ; Pyrazolones/chemistry ; Pyrazolones/pharmacology ; Structure-Activity Relationship ; Trypanocidal Agents/chemical synthesis ; Trypanocidal Agents/chemistry ; Trypanocidal Agents/pharmacology ; Trypanosoma cruzi/drug effects
    Chemical Substances Pyrazolones ; Trypanocidal Agents ; pyrazolone (39455-90-8)
    Language English
    Publishing date 2019-08-23
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2218496-X
    ISSN 1860-7187 ; 1860-7179
    ISSN (online) 1860-7187
    ISSN 1860-7179
    DOI 10.1002/cmdc.201900370
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Penicillin V, loracarbef and clindamycin in tonsillar surface fluid during acute group A streptococcal pharyngotonsillitis.

    Orrling, Arne / Kamme, Carl / Stjernquist-Desatnik, Anna

    Scandinavian journal of infectious diseases

    2005  Volume 37, Issue 6-7, Page(s) 429–435

    Abstract: Patients with acute group A- strepotococcal pharyngotonsillitis were randomly assigned to treatment for 10 d with either phenoxymethylpenicillin (PcV), loracarbef or clindamycin. The concentrations of the drugs, respectively, were determined in tonsillar ...

    Abstract Patients with acute group A- strepotococcal pharyngotonsillitis were randomly assigned to treatment for 10 d with either phenoxymethylpenicillin (PcV), loracarbef or clindamycin. The concentrations of the drugs, respectively, were determined in tonsillar surface fluid (TSF), serum and the saliva in each patient on altogether 5 occasions; before, during and 4 d after end of therapy. On the same occasions blood was drawn for analysis of C-reactive protein (CRP) and orosomucoid. On the last d of treatment PcV could be detected in TSF in 1 of 6 patients only. Loracarbef had a slower decrease in TSF during therapy and measurable levels did occur 2 d after end of therapy corresponding to MIC 100 for GAS. This may be related to the somewhat better clinical results of the cephalosporins than of PcV, and possibly indicates that an extended therapy with these drugs in primary GAS pharyngotonsillitis for more than the arbitrarily chosen 10 d could reduce the number of recurrent episodes. PcV and loracarbef were not detected in serum after the end of treatment. The concentration of clindamycin in both TSF and the saliva was fairly longstanding during therapy and reached levels exceeding MIC 100 for GAS, in both TSF and serum 2 d after the end of treatment. Several investigations have shown that GAS, especially in the stationary phase may invade respiratory epithelial cells and are present intracellularly in patients with acute pharyngotonsillitis as well as in asymptomatic carriers. The same T-type, identical DNA fingerprints and arbitrarily primed patterns are found in GAS before and after treatment failure indicating that the primary episode and the failures are caused by the same strain. The longstanding concentrations of clindamycin in TSF, roughly independent of the degree of the local inflammation combined with its intracellular accumulation and activity against resting GAS seem to explain the efficiency of the drug in recurrent GAS pharyngotonsillitis. CRP and orosomucoid were of limited value in differing between bacterial and viral pharyngtonsillitis and a correlation between antibiotic concentration and CRP/orosomucoid levels was not found.
    MeSH term(s) Adult ; Aged ; Anti-Bacterial Agents/pharmacokinetics ; Anti-Bacterial Agents/therapeutic use ; C-Reactive Protein ; Cephalosporins/pharmacokinetics ; Cephalosporins/therapeutic use ; Clindamycin/pharmacokinetics ; Clindamycin/therapeutic use ; Female ; Humans ; Male ; Middle Aged ; Orosomucoid ; Palatine Tonsil/metabolism ; Penicillin V/pharmacokinetics ; Penicillin V/therapeutic use ; Streptococcal Infections/drug therapy ; Streptococcal Infections/microbiology ; Streptococcus pyogenes ; Tissue Distribution ; Tonsillitis/drug therapy
    Chemical Substances Anti-Bacterial Agents ; Cephalosporins ; Orosomucoid ; Clindamycin (3U02EL437C) ; loracarbef (3X11EVM5SU) ; C-Reactive Protein (9007-41-4) ; Penicillin V (Z61I075U2W)
    Language English
    Publishing date 2005
    Publishing country England
    Document type Clinical Trial ; Journal Article ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 390956-6
    ISSN 1651-1980 ; 0036-5548
    ISSN (online) 1651-1980
    ISSN 0036-5548
    DOI 10.1080/00365540410020947
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Fragment-based screening in tandem with phenotypic screening provides novel antiparasitic hits.

    Blaazer, Antoni R / Orrling, Kristina M / Shanmugham, Anitha / Jansen, Chimed / Maes, Louis / Edink, Ewald / Sterk, Geert Jan / Siderius, Marco / England, Paul / Bailey, David / de Esch, Iwan J P / Leurs, Rob

    Journal of biomolecular screening

    2015  Volume 20, Issue 1, Page(s) 131–140

    Abstract: Methods to discover biologically active small molecules include target-based and phenotypic screening approaches. One of the main difficulties in drug discovery is elucidating and exploiting the relationship between drug activity at the protein target ... ...

    Abstract Methods to discover biologically active small molecules include target-based and phenotypic screening approaches. One of the main difficulties in drug discovery is elucidating and exploiting the relationship between drug activity at the protein target and disease modification, a phenotypic endpoint. Fragment-based drug discovery is a target-based approach that typically involves the screening of a relatively small number of fragment-like (molecular weight <300) molecules that efficiently cover chemical space. Here, we report a fragment screening on TbrPDEB1, an essential cyclic nucleotide phosphodiesterase (PDE) from Trypanosoma brucei, and human PDE4D, an off-target, in a workflow in which fragment hits and a series of close analogs are subsequently screened for antiparasitic activity in a phenotypic panel. The phenotypic panel contained T. brucei, Trypanosoma cruzi, Leishmania infantum, and Plasmodium falciparum, the causative agents of human African trypanosomiasis (sleeping sickness), Chagas disease, leishmaniasis, and malaria, respectively, as well as MRC-5 human lung cells. This hybrid screening workflow has resulted in the discovery of various benzhydryl ethers with antiprotozoal activity and low toxicity, representing interesting starting points for further antiparasitic optimization.
    MeSH term(s) 3',5'-Cyclic-AMP Phosphodiesterases/antagonists & inhibitors ; Antiparasitic Agents/chemistry ; Antiparasitic Agents/pharmacology ; Chagas Disease/drug therapy ; Cyclic Nucleotide Phosphodiesterases, Type 4 ; Drug Discovery/methods ; Drug Evaluation, Preclinical/methods ; Enzyme Inhibitors/chemistry ; Enzyme Inhibitors/pharmacology ; Humans ; Inhibitory Concentration 50 ; Neglected Diseases/drug therapy ; Parasitic Sensitivity Tests/methods ; Protozoan Proteins/antagonists & inhibitors ; Trypanosoma cruzi/drug effects ; Trypanosoma cruzi/enzymology
    Chemical Substances Antiparasitic Agents ; Enzyme Inhibitors ; Protozoan Proteins ; 3',5'-Cyclic-AMP Phosphodiesterases (EC 3.1.4.17) ; Cyclic Nucleotide Phosphodiesterases, Type 4 (EC 3.1.4.17) ; PDE4D protein, human (EC 3.1.4.17) ; PDEB1 protein, Trypanosoma brucei (EC 3.1.4.17)
    Language English
    Publishing date 2015-01
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1433680-7
    ISSN 1552-454X ; 1087-0571
    ISSN (online) 1552-454X
    ISSN 1087-0571
    DOI 10.1177/1087057114549735
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Patterns of Care, Tolerability, and Safety of the First Cohort of Patients Treated on a Novel High-Field MR-Linac Within the MOMENTUM Study: Initial Results From a Prospective Multi-Institutional Registry.

    de Mol van Otterloo, Sophie R / Christodouleas, John P / Blezer, Erwin L A / Akhiat, Hafid / Brown, Kevin / Choudhury, Ananya / Eggert, Dave / Erickson, Beth A / Daamen, Lois A / Faivre-Finn, Corinne / Fuller, Clifton D / Goldwein, Joel / Hafeez, Shaista / Hall, Emma / Harrington, Kevin J / van der Heide, Uulke A / Huddart, Robert A / Intven, Martijn P W / Kirby, Anna M /
    Lalondrelle, Susan / McCann, Claire / Minsky, Bruce D / Mook, Stella / Nowee, Marlies E / Oelfke, Uwe / Orrling, Kristina / Philippens, Marielle E P / Sahgal, Arjun / Schultz, Christopher J / Tersteeg, Robbert J H A / Tijssen, Rob H N / Tree, Alison C / van Triest, Baukelien / Tseng, Chia-Lin / Hall, William A / Verkooijen, Helena M

    International journal of radiation oncology, biology, physics

    2021  Volume 111, Issue 4, Page(s) 867–875

    Abstract: Purpose: High-field magnetic resonance-linear accelerators (MR-Linacs), linear accelerators combined with a diagnostic magnetic resonance imaging (MRI) scanner and online adaptive workflow, potentially give rise to novel online anatomic and response ... ...

    Abstract Purpose: High-field magnetic resonance-linear accelerators (MR-Linacs), linear accelerators combined with a diagnostic magnetic resonance imaging (MRI) scanner and online adaptive workflow, potentially give rise to novel online anatomic and response adaptive radiation therapy paradigms. The first high-field (1.5T) MR-Linac received regulatory approval in late 2018, and little is known about clinical use, patient tolerability of daily high-field MRI, and toxicity of treatments. Herein we report the initial experience within the MOMENTUM Study (NCT04075305), a prospective international registry of the MR-Linac Consortium.
    Methods and materials: Patients were included between February 2019 and October 2020 at 7 institutions in 4 countries. We used descriptive statistics to describe the patterns of care, tolerability (the percentage of patients discontinuing their course early), and safety (grade 3-5 Common Terminology Criteria for Adverse Events v.5 acute toxicity within 3 months after the end of treatment).
    Results: A total 943 patients participated in the MOMENTUM Study, 702 of whom had complete baseline data at the time of this analysis. Patients were primarily male (79%) with a median age of 68 years (range, 22-93) and were treated for 39 different indications. The most frequent indications were prostate (40%), oligometastatic lymph node (17%), brain (12%), and rectal (10%) cancers. The median number of fractions was 5 (range, 1-35). Six patients discontinued MR-Linac treatments, but none due to an inability to tolerate repeated high-field MRI. Of the 415 patients with complete data on acute toxicity at 3-month follow-up, 18 (4%) patients experienced grade 3 acute toxicity related to radiation. No grade 4 or 5 acute toxicity related to radiation was observed.
    Conclusions: In the first 21 months of our study, patterns of care were diverse with respect to clinical utilization, body sites, and radiation prescriptions. No patient discontinued treatment due to inability to tolerate daily high-field MRI scans, and the acute radiation toxicity experience was encouraging.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; Humans ; Magnetic Resonance Imaging ; Male ; Middle Aged ; Particle Accelerators ; Prospective Studies ; Radiotherapy Planning, Computer-Assisted ; Registries ; Young Adult
    Language English
    Publishing date 2021-07-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 197614-x
    ISSN 1879-355X ; 0360-3016
    ISSN (online) 1879-355X
    ISSN 0360-3016
    DOI 10.1016/j.ijrobp.2021.07.003
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Penicillin treatment failure in group A streptococcal tonsillopharyngitis: no genetic difference found between strains isolated from failures and nonfailures.

    Orrling, A / Karlsson, E / Melhus, A / Stjernquist-Desatnik, A

    The Annals of otology, rhinology, and laryngology

    2001  Volume 110, Issue 7 Pt 1, Page(s) 690–695

    Abstract: Despite penicillin (pcV) treatment, tonsillopharyngitis caused by group A streptococci (GAS) is associated with bacterial failure rates as high as 25%. The reason for this rate of failure is not fully understood. One explanation might be that certain DNA ...

    Abstract Despite penicillin (pcV) treatment, tonsillopharyngitis caused by group A streptococci (GAS) is associated with bacterial failure rates as high as 25%. The reason for this rate of failure is not fully understood. One explanation might be that certain DNA profiles of GAS strains are responsible for treatment failures. Using arbitrarily primed polymerase chain reaction (AP-PCR), we compared the DNA profiles of GAS strains from 4 patients with several treatment failures following pcV treatment of tonsillopharyngitis with the profiles of strains of the same T type from patients who were clinically and bacteriologically cured after a single course of pcV. The isolates were obtained during the same time period and from the same geographic area. Thirty-seven strains of T types 4, 12, and R28 were investigated. Eleven different DNA profiles could be detected with the AP-PCR technique. Five DNA profiles were identified as T type 12, 3 as T type 4, and 3 as T type R28. The DNA profiles of the strains from the 4 patients with several treatment failures differed, but all isolates from each one of these patients exhibited the same or a very similar profile. The DNA profiles of the failure strains were also represented in nonfailure strains. Treatment failure in these 4 patients therefore seems to be due to insufficient eradication of GAS, rather than to reinfection with a new strain. The finding that the same DNA profile can be present in both failure and nonfailure strains suggests that the treatment failure may be to some extent host-related and not only due to bacterial factors.
    MeSH term(s) Adult ; Child ; Child, Preschool ; DNA, Bacterial/genetics ; Female ; Humans ; Infant ; Male ; Microbial Sensitivity Tests ; Penicillin Resistance/genetics ; Penicillin V/adverse effects ; Penicillin V/therapeutic use ; Pharyngitis/drug therapy ; Pharyngitis/microbiology ; Polymerase Chain Reaction ; Streptococcal Infections/drug therapy ; Streptococcal Infections/microbiology ; Streptococcus pyogenes/drug effects ; Streptococcus pyogenes/genetics ; Tonsillitis/drug therapy ; Tonsillitis/microbiology ; Treatment Failure
    Chemical Substances DNA, Bacterial ; Penicillin V (Z61I075U2W)
    Language English
    Publishing date 2001-07
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 120642-4
    ISSN 1943-572X ; 0003-4894
    ISSN (online) 1943-572X
    ISSN 0003-4894
    DOI 10.1177/000348940111000716
    Database MEDical Literature Analysis and Retrieval System OnLINE

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