1.A Case of Common Variable Immune Deficiency Presenting as Recurrent Pneumococcal Pneumonia.
Juhong JEONG ; Jae Hwa CHO ; Haesung NAM ; Jeong Seon RYU ; Sung Min KWAK ; Hong Lyeol LEE
Tuberculosis and Respiratory Diseases 2011;71(4):282-285
Common variable immune deficiency (CVID) is the most common primary immune deficiency, which is manifested as chronic recurrent respiratory infections and hypoglobulinemia. CVID usually presents in the second or third decade of life. A 33-year-old woman was admitted with recurrent pneumococcal pneumonia with bacteremia and had very low levels of serum immunoglobulin G, M and A. This case emphasized a high index of suspiciousness for diagnosis of CVID in a mid-adulthood patient presenting with recurrent pneumonia with hypoglobulinemia.
Adult
;
B-Lymphocytes
;
Bacteremia
;
Common Variable Immunodeficiency
;
Female
;
Humans
;
Immunoglobulin G
;
Pneumonia
;
Pneumonia, Pneumococcal
;
Respiratory Tract Infections
2.A Case of Spinal Epidural Abscess Due to Pneumococcal Bacteremia.
Sangjoon MIN ; Juhong JEONG ; Myeongdong LEE ; Jinyeob YEO ; Seong Hyun KIM ; Jihyeon BAEK ; Jin Soo LEE ; Moon Hyeon CHEONG
Soonchunhyang Medical Science 2011;17(2):143-146
Streptococcus pneumoniae (pneumococcus) has been known to cause pneumonia, sinusitus, otitis media, meningitis, endocardiditis, myelitis and arthritis. Spinal epidural abscess by S. pneumoniae has been diagnosed rarely among the patients with spinal trauma, intravenous drug abuse, alcoholism, diabetes mellitus, long term steroid use, chronic renal failure, and acquired immune deficiency syndrome. We experienced a case of pneumococcal spinal epidural abscess occurred in 75-year-old female with L1 compression fracture since 4 years ago. Her spine magnetic resonance imaging revealed epidural abscess at the level from L3 to S1. S. pneumonia was identified on blood which was susceptible to penicillin. She was immediately treated with antibiotics and surgical exploration. The pneumococcal spinal epidural abscess is very unusual. Therefore, we report here this case with a brief review of the literature.
Acquired Immunodeficiency Syndrome
;
Aged
;
Alcoholism
;
Anti-Bacterial Agents
;
Arthritis
;
Bacteremia
;
Diabetes Mellitus
;
Epidural Abscess
;
Female
;
Fractures, Compression
;
Humans
;
Kidney Failure, Chronic
;
Magnetic Resonance Imaging
;
Meningitis
;
Myelitis
;
Otitis Media
;
Penicillins
;
Pneumonia
;
Spine
;
Streptococcus pneumoniae
;
Substance Abuse, Intravenous
3.Evaluation of the Regulatory Required Post-Authorization Safety Study for Propacetamol:Nested Case-Control and Case-Time-Control Studies
Sungho BEA ; Dongwon YOON ; Han Eol JEONG ; Juhong JUNG ; Seung-Mok PARK ; Juhee JEON ; Young-Min YE ; Jae-Hyun LEE ; Ju-Young SHIN
Yonsei Medical Journal 2024;65(2):120-128
Purpose:
Following the withdrawal of propacetamol in Europe owing to safety issues, the regulatory authority of South Korea requested a post-marketing surveillance study to investigate its safety profile.
Materials and Methods:
We conducted nested case-control and case-time-control (CTC) analyses of cases and controls identified for outcomes of interest, including anaphylaxis, thrombosis, and Stevens–Johnson syndrome (SJS), using the claims database of South Korea, 2010–2019. Risk-set sampling was used to match each case with up to 10 controls for age, sex, cohort entry date, and follow-up duration. Exposure to anaphylaxis, thrombosis, and SJS was assessed within 7, 90, and 30 days of the index date, respectively. We calculated odds ratios (OR) with 95% confidence intervals (CIs) using conditional logistic regression to assess the risk of outcomes associated with propacetamol.
Results:
We identified cases of anaphylaxis (n=61), thrombosis (n=95), and SJS (n=1) and matched them to controls (173, 268, and 4, respectively). In the nested case-control analysis, the ORs for anaphylaxis and SJS were inestimable given the small number of propacetamol users during the risk period; meanwhile, the OR for thrombosis was 1.60 (95% CI 0.71–3.62). In the CTC design, the effect estimate was only estimated for thrombosis (OR 0.56, 95% CI 0.09–3.47).
Conclusion
In both nested case-control and CTC analyses, propacetamol was not associated with an increased risk of anaphylaxis, thrombosis, or SJS. The findings from this study, which used routinely collected clinical data, provide reassuring real-world evidence regarding the safety of propacetamol in a nationwide population to support regulatory decision-making.