Comparison of safety between high and low doses of sulbactam/ampicillin: A retrospective observational study in Japanese patients with pneumonia
Autor: | Takashi Miyabe, Kazutaka Yamauchi, Ichiro Nakakura, Kaori Imanishi, Rumi Sako |
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Rok vydání: | 2020 |
Předmět: |
Adult
0301 basic medicine Microbiology (medical) medicine.medical_specialty Anemia 030106 microbiology Hematocrit Gastroenterology 03 medical and health sciences 0302 clinical medicine Japan Internal medicine medicine Humans Pharmacology (medical) Aspartate Aminotransferases 030212 general & internal medicine Adverse effect Blood urea nitrogen Retrospective Studies medicine.diagnostic_test business.industry Incidence (epidemiology) Pneumonia Sulbactam medicine.disease Elevated alkaline phosphatase Infectious Diseases Propensity score matching Ampicillin Drug Therapy Combination medicine.symptom business medicine.drug |
Zdroj: | Journal of Infection and Chemotherapy. 26:1152-1157 |
ISSN: | 1341-321X |
DOI: | 10.1016/j.jiac.2020.06.004 |
Popis: | Although 12 g/day sulbactam/ampicillin (SBT/ABPC) is approved in Japan, differences in the frequency of adverse effects induced by conventional (≤6 g/day) and high (≥9 g/day) doses remain unclear. We performed a retrospective observational study on SBT/ABPC-treated hospitalized adult patients with pneumonia from October 2015 to January 2018 to compare the safety between high and low doses. Patients were divided into high-dose (≥9 g/day, n = 200) and low-dose (≤6 g/day, n = 246) groups. We used logistic regression to determine propensity scores for the high-dose and low-dose groups and compared the incidence of adverse effects after propensity score adjustment (n = 200 in each group). Following propensity score adjustment, the frequency of elevated alanine aminotransferase (ALT) level was still significantly higher in the high-dose group than in the low-dose group (21% versus 11%, p = 0.006). In contrast, the frequencies of elevated alkaline phosphatase, aspartate aminotransferase, and serum creatinine levels and decreased white blood cell and platelet counts, and incidence of anemia, were not. Changes in blood urea nitrogen levels, erythrocyte count, and hematocrit were not significantly different between the two dose groups. There were two cases of rash reported to the Pharmaceuticals and Medical Devices Agency as an adverse effect in the high-dose group. Thirty-day mortality rates were not significantly different after propensity score adjustment. Our analysis suggests that an increase in the ALT grade was more frequent in patients treated with a daily dose of SBT/ABPC of ≥9 g. |
Databáze: | OpenAIRE |
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