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  1. Article ; Online: Establishing the safety of phenobarbital treatment of alcohol withdrawal syndrome on general medical wards: A retrospective cohort study.

    Ronan, Matthew V / Ganatra, Rahul B / Saukkonen, Jussi

    Alcohol (Fayetteville, N.Y.)

    2023  Volume 116, Page(s) 29–34

    Abstract: Introduction: Concern about adverse effects from phenobarbital limits its use in treating alcohol withdrawal syndrome (AWS) on general medical wards. Benzodiazepines are the recommended treatment for inpatient management of AWS, yet a subset of patients ...

    Abstract Introduction: Concern about adverse effects from phenobarbital limits its use in treating alcohol withdrawal syndrome (AWS) on general medical wards. Benzodiazepines are the recommended treatment for inpatient management of AWS, yet a subset of patients have an inadequate response or experience complications of AWS despite treatment with benzodiazepines. Data supporting an alternative treatment are needed. We set out to estimate the rate of serious adverse events (SAEs) of phenobarbital treatment for AWS on general medical wards.
    Methods: Retrospective cohort study of all general medical ward patients hospitalized at a single tertiary urban VA Medical Center from October 2018-May 2021 who received phenobarbital for treatment of AWS. Primary outcomes were SAEs attributed to phenobarbital and treatment failure. SAEs were defined as ICU transfer or intubation for over-sedation, pneumonia, and death. Treatment failure was defined as progression of withdrawal resulting in seizure, ICU transfer, behavioral emergencies, or death.
    Results: During the study period, phenobarbital was administered in 29% (244) of all AWS hospitalizations. Among them, 93% had a history of AWS hospitalization and 68% had a history of complicated AWS. Fifty-three percent of patients met criteria for moderate, severe, or complicated withdrawal prior to phenobarbital initiation. The mean cumulative dose of phenobarbital per patient was 966.5 mg (13.6 mg/kg). SAEs occurred in 1 of 244 hospitalizations (0.4%): there were no intubations, ICU transfers for oversedation, or deaths due to phenobarbital or AWS. One case of pneumonia was possibly attributable to phenobarbital. Treatment failures (6 ICU transfers, 9 behavioral emergencies) were identified during 12 of 244 hospitalizations (4.9%).
    Conclusions: SAEs and treatment failures were infrequent among 148 patients treated with phenobarbital across 244 hospitalizations with a mean cumulative dose of 966.5 mg per patient. Our findings suggest that phenobarbital is a safe alternative treatment of AWS in general medical ward patients.
    MeSH term(s) Humans ; Substance Withdrawal Syndrome/drug therapy ; Substance Withdrawal Syndrome/epidemiology ; Alcoholism/drug therapy ; Alcoholism/epidemiology ; Retrospective Studies ; Emergencies ; Benzodiazepines/adverse effects ; Phenobarbital/adverse effects ; Pneumonia/chemically induced
    Chemical Substances Benzodiazepines (12794-10-4) ; Phenobarbital (YQE403BP4D)
    Language English
    Publishing date 2023-11-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 605912-0
    ISSN 1873-6823 ; 0741-8329
    ISSN (online) 1873-6823
    ISSN 0741-8329
    DOI 10.1016/j.alcohol.2023.10.005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: From the Heart.

    Garfinkel, Amanda C / Vaidya, Anand / Strymish, Judith / Brecher, Stephen M / Saukkonen, Jussi

    The New England journal of medicine

    2023  Volume 389, Issue 8, Page(s) e14

    MeSH term(s) Humans ; Heart ; Thorax
    Language English
    Publishing date 2023-08-23
    Publishing country United States
    Document type Case Reports ; Journal Article
    ZDB-ID 207154-x
    ISSN 1533-4406 ; 0028-4793
    ISSN (online) 1533-4406
    ISSN 0028-4793
    DOI 10.1056/NEJMimc2214471
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Challenges in reintroducing tuberculosis medications after hepatotoxicity.

    Saukkonen, Jussi

    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

    2010  Volume 50, Issue 6, Page(s) 840–842

    MeSH term(s) Antitubercular Agents/administration & dosage ; Antitubercular Agents/adverse effects ; Antitubercular Agents/therapeutic use ; Chemical and Drug Induced Liver Injury ; Drug Therapy, Combination/methods ; Humans ; Treatment Outcome ; Tuberculosis/complications ; Tuberculosis/drug therapy
    Chemical Substances Antitubercular Agents
    Language English
    Publishing date 2010-03-15
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 1099781-7
    ISSN 1537-6591 ; 1058-4838
    ISSN (online) 1537-6591
    ISSN 1058-4838
    DOI 10.1086/650577
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Monitoring for tuberculosis drug hepatotoxicity: moving from opinion to evidence.

    Saukkonen, Jussi J / Powell, Krista / Jereb, John A

    American journal of respiratory and critical care medicine

    2012  Volume 185, Issue 6, Page(s) 598–599

    MeSH term(s) Antitubercular Agents/therapeutic use ; Chemical and Drug Induced Liver Injury/prevention & control ; Female ; Humans ; Liver Function Tests/standards ; Male ; Monitoring, Physiologic/standards ; Practice Guidelines as Topic ; Tuberculosis/drug therapy
    Chemical Substances Antitubercular Agents
    Language English
    Publishing date 2012-03-15
    Publishing country United States
    Document type Editorial ; Comment
    ZDB-ID 1180953-x
    ISSN 1535-4970 ; 0003-0805 ; 1073-449X
    ISSN (online) 1535-4970
    ISSN 0003-0805 ; 1073-449X
    DOI 10.1164/rccm.201112-2174ED
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Book: Über das Vorkommen von freien Nucleotiden in ruhenden und wachsenden Geweben

    Saukkonen, Jussi J.

    (Annales medicinae experimentalis et biologiae Fenniae ; 34, Suppl. 3)

    1956  

    Author's details von Jussi J. Saukkonen
    Series title Annales medicinae experimentalis et biologiae Fenniae ; 34, Suppl. 3
    Collection
    Language German
    Size 78 S. ; 8-o
    Publisher Mercatorin Kirjap
    Publishing place Helsinki
    Publishing country Finland
    Document type Book
    HBZ-ID HT010313210
    Database Catalogue ZB MED Medicine, Health

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  6. Article ; Online: Community-acquired Pneumonia Guideline Recommendations-Impact of a Consensus-based Process versus Systematic Reviews.

    Wilson, Kevin C / Schoenberg, Noah C / Cohn, David L / Crothers, Kristina / Fennelly, Kevin P / Metlay, Joshua P / Saukkonen, Jussi J / Strange, Charlie / Waterer, Grant / Dweik, Raed

    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

    2020  Volume 73, Issue 7, Page(s) e1467–e1475

    Abstract: Background: The American Thoracic Society (ATS)/Infectious Diseases Society of America (IDSA) Community-acquired Pneumonia (CAP) guidelines were developed using systematic reviews to inform every recommendation, as suggested by the Institute of Medicine ...

    Abstract Background: The American Thoracic Society (ATS)/Infectious Diseases Society of America (IDSA) Community-acquired Pneumonia (CAP) guidelines were developed using systematic reviews to inform every recommendation, as suggested by the Institute of Medicine Standards for Trustworthy Guidelines. Recent studies suggest that an expert consensus-based approach, called the Convergence of Opinion on Recommendations and Evidence (CORE) process, can produce recommendations that are concordant with recommendations informed by systematic reviews.
    Purpose: The goal of the study was to evaluate the efficacy of the CORE process had it been used to develop the ATS/IDSA CAP guidelines.
    Methods: Experts in CAP who were not on the guideline panel and had no knowledge of the guideline's systematic reviews or recommendations were recruited to participate in the CORE process, addressing the same questions asked by the guideline panel. Recommendations derived from the CORE process were compared to the guideline recommendations. Concordance of the course of action, strength of recommendation, and quality of evidence were determined.
    Results: Using a threshold of 70% of experts selecting the same course of action to make a recommendation, the CORE process yielded a recommendation for 20 of 31 (65%) questions. Among the 20 CORE-derived recommendations, 19 (95%) were concordant with the guideline recommendations (kappa agreement 0.88, 95% CI .64-1.00). There was less agreement among the strength of recommendations (58%) and quality of evidence (42%).
    Conclusions: If the CORE process had been used, 11 systematic reviews would have been necessary rather than 31, with minimal impact on the recommended courses of action.
    MeSH term(s) Community-Acquired Infections/drug therapy ; Consensus ; Humans ; Pneumonia/drug therapy
    Language English
    Publishing date 2020-09-21
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1099781-7
    ISSN 1537-6591 ; 1058-4838
    ISSN (online) 1537-6591
    ISSN 1058-4838
    DOI 10.1093/cid/ciaa1428
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Rifampin and pyrazinamide for latent tuberculosis infection: clinical trials and general practice.

    Saukkonen, Jussi

    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

    2004  Volume 39, Issue 4, Page(s) 566–568

    MeSH term(s) Clinical Trials as Topic ; Family Practice ; Humans ; Pyrazinamide/therapeutic use ; Rifampin/therapeutic use ; Tuberculosis/drug therapy ; Tuberculosis/microbiology
    Chemical Substances Pyrazinamide (2KNI5N06TI) ; Rifampin (VJT6J7R4TR)
    Language English
    Publishing date 2004-08-15
    Publishing country United States
    Document type Comment ; Editorial ; Review
    ZDB-ID 1099781-7
    ISSN 1537-6591 ; 1058-4838
    ISSN (online) 1537-6591
    ISSN 1058-4838
    DOI 10.1086/422728
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Nonparticipation reasons in a randomized international trial of a new latent tuberculosis infection regimen.

    Hedges, Kimberley N Chapman / Borisov, Andrey S / Saukkonen, Jussi J / Scott, Nigel A / Hecker, Emily J / Bozeman, Lorna / Dukes Hamilton, Carol / Kerrigan, Amy / Bessler, Patricia / Moreno-Martinez, Antonio / Arevalo, Bert / Goldberg, Stefan V

    Clinical trials (London, England)

    2019  Volume 17, Issue 1, Page(s) 39–51

    Abstract: Background/aims: Efficient recruitment of eligible participants, optimizing time and sample size, is a crucial component in conducting a successful clinical trial. Inefficient participant recruitment can impede study progress, consume staff time and ... ...

    Abstract Background/aims: Efficient recruitment of eligible participants, optimizing time and sample size, is a crucial component in conducting a successful clinical trial. Inefficient participant recruitment can impede study progress, consume staff time and resources, and limit quality and generalizability or the power to assess outcomes. Recruitment for disease prevention trials poses additional challenges because patients are asymptomatic. We evaluated candidates for a disease prevention trial to determine reasons for nonparticipation and to identify factors that can be addressed to improve recruitment efficiency.
    Methods: During 2001-2009, the Tuberculosis Trials Consortium conducted Study 26 (PREVENT TB), a randomized clinical trial at 26 sites in four countries, among persons with latent tuberculosis infection at high risk for tuberculosis disease progression, comparing 3 months of directly observed once-weekly rifapentine plus isoniazid with 9 months of self-administered daily isoniazid. During March 2005-February 2008, non-identifying demographic information, risk factors for experiencing active tuberculosis disease, and reasons for not enrolling were collected from screened patients to facilitate interpretation of trial data, to meet Consolidated Standards of Reporting Trials standards, and to evaluate reasons for nonparticipation.
    Results: Of the 7452 candidates screened in Brazil, Canada, Spain, and the United States, 3584 (48%) were not enrolled, because of ineligibility (41%), site decision (10%), or patient choice (49%). Among those who did not enroll by own choice, and for whom responses were recorded on whether they would accept treatment outside of the study (n = 1430), 68% reported that they planned to accept non-study latent tuberculosis infection treatment. Among 1305 patients with one or more reported reasons for nonparticipation, study staff recorded a total of 1886 individual reasons (reason count: median = 1/patient; range = 1-9) for why patients chose not to enroll, including grouped concerns about research (24% of 1886), work or school conflicts (20%), medication or health beliefs (16%), latent tuberculosis infection beliefs (11%), and patient lifestyle and family concerns (10%).
    Conclusion: Educational efforts addressing clinical research concerns and beliefs about medication and health, as well as study protocols that accommodate patient-related concerns (e.g. work, school, and lifestyle) might increase willingness to enter clinical trials. Findings from this evaluation can support development of communication and education materials for clinical trial sites at the beginning of a trial to allow study staff to address potential participant concerns during study screening.
    MeSH term(s) Adolescent ; Adult ; Antitubercular Agents/therapeutic use ; Child ; Child, Preschool ; Clinical Trials, Phase III as Topic ; Drug Therapy, Combination ; Female ; Humans ; Isoniazid/therapeutic use ; Latent Tuberculosis/drug therapy ; Latent Tuberculosis/prevention & control ; Male ; Patient Selection ; Randomized Controlled Trials as Topic/methods ; Refusal to Participate ; Rifampin/analogs & derivatives ; Rifampin/therapeutic use ; Risk Factors ; Young Adult
    Chemical Substances Antitubercular Agents ; Isoniazid (V83O1VOZ8L) ; Rifampin (VJT6J7R4TR) ; rifapentine (XJM390A33U)
    Language English
    Publishing date 2019-11-06
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 2138796-5
    ISSN 1740-7753 ; 1740-7745
    ISSN (online) 1740-7753
    ISSN 1740-7745
    DOI 10.1177/1740774519885380
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Acute respiratory failure from abused substances.

    Wilson, Kevin C / Saukkonen, Jussi J

    Journal of intensive care medicine

    2004  Volume 19, Issue 4, Page(s) 183–193

    Abstract: Acute respiratory failure is a common complication of drug abuse. It is more likely to develop in the setting of chronic lung disease or debility in those with limited respiratory reserve. Drugs may acutely precipitate respiratory failure by compromising ...

    Abstract Acute respiratory failure is a common complication of drug abuse. It is more likely to develop in the setting of chronic lung disease or debility in those with limited respiratory reserve. Drugs may acutely precipitate respiratory failure by compromising respiratory pump function and/or by causing pulmonary pathology. Polysubstance overdoses are common, and clinicians should anticipate complications related to multiple drugs. Impairment of respiratory pump function may develop from central nervous system (CNS) depression (suppression of the medulla oblongata, stroke or seizures) or respiratory muscle fatigue (increased respiratory workload, metabolic acidosis). Drug-related respiratory pathology may result from parenchymal (aspiration-related events, pulmonary edema, hemorrhage, pneumothorax, infectious and non-infectious pneumonitides), airway (bronchospasm and hemorrhage), or pulmonary vascular insults (endovascular infections, hemorrhage, and vasoconstrictive events). Alcohol, cocaine, amphetamines, opiates, and benzodiazepines are the most commonly abused drugs that may induce events leading to acute respiratory failure. While decontamination and aggressive supportive measures are indicated, specific therapies to correct seizures, metabolic acidosis, pneumothorax, infections, bronchospasm, and agitation should be considered. Drug-related respiratory failure when due to CNS depression alone may portend well, but in patients with drug-related significant pulmonary pathology, a protracted course of illness may be anticipated.
    MeSH term(s) Acute Disease ; Administration, Inhalation ; Alcoholism/complications ; Amphetamines/poisoning ; Benzodiazepines/poisoning ; Bronchial Spasm/etiology ; Cannabis/poisoning ; Cocaine/poisoning ; Critical Care/methods ; Humans ; Narcotics/poisoning ; Pneumonia/etiology ; Pneumothorax/etiology ; Pulmonary Edema/etiology ; Respiratory Distress Syndrome, Adult/etiology ; Respiratory Insufficiency/etiology ; Respiratory Insufficiency/physiopathology ; Respiratory Physiological Phenomena/drug effects ; Respiratory Tract Infections/etiology ; Solvents/poisoning ; Substance-Related Disorders/complications
    Chemical Substances Amphetamines ; Narcotics ; Solvents ; Benzodiazepines (12794-10-4) ; Cocaine (I5Y540LHVR)
    Language English
    Publishing date 2004-07
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 632828-3
    ISSN 1525-1489 ; 0885-0666
    ISSN (online) 1525-1489
    ISSN 0885-0666
    DOI 10.1177/0885066604263918
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Predicting non-completion of treatment for latent tuberculous infection: a prospective survey.

    Shieh, Fred K / Snyder, Graham / Horsburgh, C Robert / Bernardo, John / Murphy, Claire / Saukkonen, Jussi J

    American journal of respiratory and critical care medicine

    2006  Volume 174, Issue 6, Page(s) 717–721

    Abstract: Unlabelled: Treatment of latent tuberculosis (TB) infection (LTBI) is essential for the elimination of TB in the United States, but treatment is often not completed. Little is known about patients' reasons for not completing treatment. We hypothesized ... ...

    Abstract Unlabelled: Treatment of latent tuberculosis (TB) infection (LTBI) is essential for the elimination of TB in the United States, but treatment is often not completed. Little is known about patients' reasons for not completing treatment. We hypothesized that certain health beliefs, lifestyle, and clinic- and regimen-related barriers to provision of care could predict non-completion of LTBI treatment.
    Methods: We administered a survey in English, Chinese, or Spanish to patients with LTBI at the first TB clinic visit. Using chi(2) and logistic regression analysis, we assessed demographics, TB risk factors, and survey responses as predictors of non-completion of 6 mo of isoniazid.
    Results: 217 patients, 90% foreign-born, completed the survey, and 28.6% of which finished at least 6 mo of isoniazid under usual clinic conditions. Multivariate analysis identified two independent predictors of non-completion: low risk perception of progressing to active TB without LTBI treatment (odds ratio [OR], 0.31 [0.13-0.72], 95% confidence interval [CI]), p = 0.007, accounting for 20% of non-completers, and not wanting venipuncture (OR, 0.43 [0.22-0.85], 95% CI), p = 0.015, accounting for 37% of non-completers. Another 18% shared both predictors; thus these two predictors accounted for 75% of non-completers in total.
    Conclusions: Patients assess LTBI treatment risks and inconveniences relative to low perceived benefits at treatment outset. Predictors of LTBI treatment non-completion are identifiable at the first visit. Targeting TB high-risk individuals, minimizing inconveniences, further education, and use of diagnostic tests with improved specificity for TB may address these concerns.
    MeSH term(s) Adult ; Antitubercular Agents/therapeutic use ; Female ; Humans ; Incidence ; Isoniazid/therapeutic use ; Male ; Massachusetts/epidemiology ; Patient Compliance ; Population Surveillance ; Prognosis ; Prospective Studies ; Risk Factors ; Treatment Failure ; Tuberculosis/drug therapy ; Tuberculosis/epidemiology
    Chemical Substances Antitubercular Agents ; Isoniazid (V83O1VOZ8L)
    Language English
    Publishing date 2006-09-15
    Publishing country United States
    Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1180953-x
    ISSN 1535-4970 ; 1073-449X ; 0003-0805
    ISSN (online) 1535-4970
    ISSN 1073-449X ; 0003-0805
    DOI 10.1164/rccm.200510-1667OC
    Database MEDical Literature Analysis and Retrieval System OnLINE

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