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  1. Artikel ; Online: Direct-Acting Antiviral Therapy for Patients with Chronic Hepatitis C Infection and Decompensated Cirrhosis.

    Pearlman, Brian L

    Digestive diseases and sciences

    2024  Band 69, Heft 5, Seite(n) 1551–1561

    Abstract: Patients with chronic hepatitis C virus (HCV) infection and decompensated cirrhosis are an important population for antiviral therapy yet under-represented in clinical trials. HCV direct-acting antiviral (DAA) therapies, unlike interferon-containing ... ...

    Abstract Patients with chronic hepatitis C virus (HCV) infection and decompensated cirrhosis are an important population for antiviral therapy yet under-represented in clinical trials. HCV direct-acting antiviral (DAA) therapies, unlike interferon-containing regimens, can be safely utilized in decompensated patients. Per guidelines from the American Association for the Study of Liver Diseases (AASLD), therapy of choice in HCV and decompensated cirrhosis is sofosbuvir, an HCV polymerase inhibitor, combined with a replication complex inhibitor (NS5A inhibitor) with or without ribavirin. Combination therapy with a HCV protease inhibitor and an NS5A inhibitor is effective in this population but is specifically not recommended in AASLD guidelines due to safety concerns. Important risk factors for further decompensation during DAA therapy are serum albumin < 3.5 g/dL, MELD (Model for End-Stage Liver Disease) score > 14, or HCV genotype 3 infection. Although sustained virologic response (SVR) is achieved less often in patients with decompensated vs compensated cirrhosis, in clinical studies response rates are > 80%. Both Child-Turcotte-Pugh Class at baseline and viral genotype can affect these response rates. Achieving SVR lowers risk of mortality, but to a lesser extent than in individuals with compensated cirrhosis. Likewise, treating patients for HCV infection along with successful treatment for hepatocellular carcinoma improves risks of both liver-related and overall mortality. In fewer than one third of cases, treating transplant-eligible, HCV-infected patients pre-transplant enables their delisting from transplant wait lists.
    Mesh-Begriff(e) Humans ; Antiviral Agents/therapeutic use ; Hepatitis C, Chronic/drug therapy ; Hepatitis C, Chronic/complications ; Liver Cirrhosis/virology ; Liver Cirrhosis/drug therapy ; Drug Therapy, Combination ; Hepacivirus/genetics ; Hepacivirus/drug effects ; Sustained Virologic Response ; Sofosbuvir/therapeutic use
    Sprache Englisch
    Erscheinungsdatum 2024-04-05
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Review
    ZDB-ID 304250-9
    ISSN 1573-2568 ; 0163-2116
    ISSN (online) 1573-2568
    ISSN 0163-2116
    DOI 10.1007/s10620-024-08393-x
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: A Patient With Jaundice and Malaise.

    Pearlman, Brian L

    JAMA

    2022  Band 327, Heft 24, Seite(n) 2448–2449

    Mesh-Begriff(e) Humans ; Jaundice/etiology
    Sprache Englisch
    Erscheinungsdatum 2022-06-13
    Erscheinungsland United States
    Dokumenttyp Case Reports ; Journal Article
    ZDB-ID 2958-0
    ISSN 1538-3598 ; 0254-9077 ; 0002-9955 ; 0098-7484
    ISSN (online) 1538-3598
    ISSN 0254-9077 ; 0002-9955 ; 0098-7484
    DOI 10.1001/jama.2022.8384
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Nasal Deviation and Facial Asymmetry in Patients Undergoing Rhinoplasty.

    Scott, Brian L / Pearlman, Steven

    Aesthetic surgery journal

    2024  

    Abstract: Background: Existing literature conflicts on whether nasal deviation is primarily attributable to trauma or the result of asymmetric facial development.: Objectives: Establish the prevalence of nasal trauma and facial asymmetry in patients undergoing ...

    Abstract Background: Existing literature conflicts on whether nasal deviation is primarily attributable to trauma or the result of asymmetric facial development.
    Objectives: Establish the prevalence of nasal trauma and facial asymmetry in patients undergoing rhinoplasty. Determine if a correlation exists between the laterality of facial asymmetry and nasal deviation.
    Methods: Retrospective review of patients who underwent primary rhinoplasty with the senior author over a 12-month period. Patient charts were reviewed and clinical photographs were analyzed.
    Results: 144 patients underwent rhinoplasty over the study period. 68 patients underwent revision rhinoplasty and were excluded. Of the 76 patients who underwent primary rhinoplasty, 9% reported prior nasal trauma, 68% had deviated nasal bones, 46% had deviated nasal tips, 70% had asymmetric midfaces, and 36% had deviated chins. In patients without prior trauma history, nasal bones were most commonly deviated towards the side of midface hypoplasia (53%, p=0.008). The nasal tip was most commonly deviated contralateral to the side of septal deviation (59%, p=0.001). There was no association between nasal bone and chin deviation. Nasal tip deviation was not associated with midface hypoplasia or chin deviation.
    Conclusions: Nasal deviation is primarily driven by asymmetric facial growth rather than the result of nasal trauma.
    Sprache Englisch
    Erscheinungsdatum 2024-06-04
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 2087022-X
    ISSN 1527-330X ; 1090-820X ; 1084-0761
    ISSN (online) 1527-330X
    ISSN 1090-820X ; 1084-0761
    DOI 10.1093/asj/sjae125
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Buch: Challenging cases in the management of hepatitis C viral infection

    Pearlman, Brian L.

    a case study compendium

    (Gastroenterology & hepatology ; 5,4, Suppl. 11)

    2009  

    Verfasserangabe faculty Brian Pearlman
    Serientitel Gastroenterology & hepatology ; 5,4, Suppl. 11
    Überordnung
    Sprache Englisch
    Umfang 14 S. : Ill.
    Verlag Gastro-Hep Comm
    Erscheinungsort New York, NY
    Erscheinungsland Vereinigte Staaten
    Dokumenttyp Buch
    HBZ-ID HT015936000
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  5. Artikel ; Online: How Would You Manage This Patient With Nonalcoholic Fatty Liver Disease?

    Pearlman, Brian L

    Annals of internal medicine

    2019  Band 171, Heft 11, Seite(n) 861–862

    Mesh-Begriff(e) Humans ; Israel ; Liver ; Non-alcoholic Fatty Liver Disease ; Teaching Rounds
    Sprache Englisch
    Erscheinungsdatum 2019-12-02
    Erscheinungsland United States
    Dokumenttyp Letter ; Comment
    ZDB-ID 336-0
    ISSN 1539-3704 ; 0003-4819
    ISSN (online) 1539-3704
    ISSN 0003-4819
    DOI 10.7326/L19-0667
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Buch: Treatment options for HCV nonresponders and relapse patients

    Pearlman, Brian L. / Sjogren, Maria H.

    (Gastroenterology & hepatology ; 6,3, Suppl. 6 : Clinical roundtable monograph)

    2010  

    Verfasserangabe faculty Brian L. Pearlman ; Maria H. Sjogren
    Serientitel Gastroenterology & hepatology ; 6,3, Suppl. 6 : Clinical roundtable monograph
    Überordnung
    Sprache Englisch
    Umfang 10 S. : graph. Darst.
    Verlag Gastro-Hep Communications
    Erscheinungsort New York, NY
    Erscheinungsland Vereinigte Staaten
    Dokumenttyp Buch
    HBZ-ID HT016677437
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  7. Artikel ; Online: Simulation-based Exercises to Improve the Performance of Cosmetic Consultations.

    Ahmed, Areeba / Wilson, Sarah / Kyllo, Rachel L / Koza, Eric / Shi, Victoria / Haq, Misha / Ma, Melissa / Poon, Emily / Worley, Brandon / Harikumar, Vishnu / Pearlman, Ross / Schlessinger, Daniel I / Cahn, Brian A / Alam, Murad

    Journal of the American Academy of Dermatology

    2024  

    Sprache Englisch
    Erscheinungsdatum 2024-05-03
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 603641-7
    ISSN 1097-6787 ; 0190-9622
    ISSN (online) 1097-6787
    ISSN 0190-9622
    DOI 10.1016/j.jaad.2024.04.065
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: Review article: novel antivirals for hepatitis C-sofosbuvir/velpatasvir/voxilaprevir, glecaprevir/pibrentasvir.

    Pearlman, Brian L / Hinds, Andrew E

    Alimentary pharmacology & therapeutics

    2018  Band 48, Heft 9, Seite(n) 914–923

    Abstract: Background: In 2017, the hepatitis C treatment regimens sofosbuvir/velpatasvir/voxilaprevir (SOF/VEL/VOX) and glecaprevir/pibrentasvir (G/P) received approval from the U.S. Food and Drug Administration. Although both SOF/VEL/VOX (NS5B polymerase ... ...

    Abstract Background: In 2017, the hepatitis C treatment regimens sofosbuvir/velpatasvir/voxilaprevir (SOF/VEL/VOX) and glecaprevir/pibrentasvir (G/P) received approval from the U.S. Food and Drug Administration. Although both SOF/VEL/VOX (NS5B polymerase inhibitor/NS5A inhibitor/NS3/4A protease inhibitor) and G/P (NS3/4A protease inhibitor/NS5A inhibitor) are pangenotypic regimens, they are indicated for distinct subsets of patients with hepatitis C.
    Aim: To compare and contrast available safety and efficacy data for SOF/VEL/VOX and G/P and outline their clinical utility.
    Methods: For each of the regimens, this review outlines the indications, safety information, and the major clinical studies in which SOF/VEL/VOX and G/P were evaluated.
    Results: SOF/VEL/VOX is positioned as a salvage regimen for patients previously treated with NS5A inhibitors and for genotype 1a- and 3-infected patients who had failed other sofosbuvir-containing regimens. G/P is the first pangenotypic regimen with an 8-week duration for treatment-naïve, non-cirrhotic patients, and it is indicated for patients with any genotype who have advanced kidney disease, including those on dialysis.
    Conclusion: The addition of SOF/VEL/VOX and G/P to existing hepatitis C treatment options will expand the number of patients who are eligible for and responsive to treatment, thus increasing the possibility of eliminating hepatitis C as a public health issue.
    Mesh-Begriff(e) Antiviral Agents/therapeutic use ; Benzimidazoles/therapeutic use ; Carbamates/therapeutic use ; Clinical Trials, Phase III as Topic/methods ; Hepatitis C, Chronic/diagnosis ; Hepatitis C, Chronic/drug therapy ; Hepatitis C, Chronic/epidemiology ; Heterocyclic Compounds, 4 or More Rings/therapeutic use ; Humans ; Macrocyclic Compounds/therapeutic use ; Quinoxalines/therapeutic use ; Sofosbuvir/therapeutic use ; Sulfonamides/therapeutic use
    Chemische Substanzen Antiviral Agents ; Benzimidazoles ; Carbamates ; Heterocyclic Compounds, 4 or More Rings ; Macrocyclic Compounds ; Quinoxalines ; Sulfonamides ; voxilaprevir (0570F37359) ; pibrentasvir (2WU922TK3L) ; glecaprevir (K6BUU8J72P) ; velpatasvir (KCU0C7RS7Z) ; Sofosbuvir (WJ6CA3ZU8B)
    Sprache Englisch
    Erscheinungsdatum 2018-10-04
    Erscheinungsland England
    Dokumenttyp Journal Article ; Review
    ZDB-ID 639012-2
    ISSN 1365-2036 ; 0269-2813 ; 0953-0673
    ISSN (online) 1365-2036
    ISSN 0269-2813 ; 0953-0673
    DOI 10.1111/apt.14977
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel ; Online: Protease inhibitors for the treatment of chronic hepatitis C genotype-1 infection: the new standard of care.

    Pearlman, Brian L

    The Lancet. Infectious diseases

    2012  Band 12, Heft 9, Seite(n) 717–728

    Abstract: For the past decade, the standard treatment for chronic hepatitis C infection has been pegylated-interferon plus ribavirin. With US Food and Drug Administration approval of boceprevir and telaprevir--two protease inhibitors--the standard-of-care ... ...

    Abstract For the past decade, the standard treatment for chronic hepatitis C infection has been pegylated-interferon plus ribavirin. With US Food and Drug Administration approval of boceprevir and telaprevir--two protease inhibitors--the standard-of-care treatment for genotype-1 infection, the main genotype worldwide, is now peginterferon plus ribavirin and a protease inhibitor. Rates of sustained virological response or cure with triple combination treatment have improved substantially, both in patients who have had previous treatment and in those who have not. Improvements have been most substantial in populations regarded as difficult to treat, such as individuals with cirrhosis. However, despite improved response rates, protease inhibitors have incremental toxic effects, high costs, increased pill burden, and many drug interactions. Moreover, because new antiviral drugs directly inhibit hepatitis C virus, viral resistance has become an important issue, essentially precluding use of protease inhibitor monotherapy, and potentially restricting future treatment options for patients who consequently do not achieve sustained virological response. Protease inhibitors are the first of many antiviral medications that will probably be combined in future interferon-free regimens.
    Mesh-Begriff(e) Antiviral Agents/administration & dosage ; Antiviral Agents/adverse effects ; Drug Resistance, Viral ; Drug Therapy, Combination/adverse effects ; Drug Therapy, Combination/methods ; Genotype ; Hepacivirus/classification ; Hepacivirus/genetics ; Hepacivirus/isolation & purification ; Hepatitis C, Chronic/drug therapy ; Hepatitis C, Chronic/virology ; Humans ; Interferon-alpha/administration & dosage ; Oligopeptides/administration & dosage ; Oligopeptides/adverse effects ; Polyethylene Glycols/administration & dosage ; Proline/administration & dosage ; Proline/adverse effects ; Proline/analogs & derivatives ; Protease Inhibitors/administration & dosage ; Protease Inhibitors/adverse effects ; Recombinant Proteins/administration & dosage ; Ribavirin/administration & dosage ; Standard of Care/trends ; United States
    Chemische Substanzen Antiviral Agents ; Interferon-alpha ; Oligopeptides ; Protease Inhibitors ; Recombinant Proteins ; Polyethylene Glycols (30IQX730WE) ; Ribavirin (49717AWG6K) ; telaprevir (655M5O3W0U) ; N-(3-amino-1-(cyclobutylmethyl)-2,3-dioxopropyl)-3-(2-((((1,1-dimethylethyl)amino)carbonyl)amino)-3,3-dimethyl-1-oxobutyl)-6,6-dimethyl-3-azabicyclo(3.1.0)hexan-2-carboxamide (89BT58KELH) ; Proline (9DLQ4CIU6V) ; peginterferon alfa-2a (Q46947FE7K)
    Sprache Englisch
    Erscheinungsdatum 2012-09
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Review
    ZDB-ID 2061641-7
    ISSN 1474-4457 ; 1473-3099
    ISSN (online) 1474-4457
    ISSN 1473-3099
    DOI 10.1016/S1473-3099(12)70060-9
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: Metabolic effects of tumescent liposuction.

    Ahmed, Areeba / Kyllo, Rachel L / Koza, Eric / Haq, Misha / Shi, Victoria J / Ma, Melissa / Weil, Alexandra / Wan, Hoi Ting / Poon, Emily / Pearlman, Ross / Schlessinger, Daniel I / Cahn, Brian A / Alam, Murad

    Archives of dermatological research

    2023  Band 316, Heft 1, Seite(n) 59

    Mesh-Begriff(e) Humans ; Lipectomy/adverse effects ; Lidocaine ; Anesthesia, Local
    Chemische Substanzen Lidocaine (98PI200987)
    Sprache Englisch
    Erscheinungsdatum 2023-12-27
    Erscheinungsland Germany
    Dokumenttyp Letter
    ZDB-ID 130131-7
    ISSN 1432-069X ; 0340-3696
    ISSN (online) 1432-069X
    ISSN 0340-3696
    DOI 10.1007/s00403-023-02809-w
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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