Correlation of effectiveness and tolerability assessments from a pharmacy-based observational study investigating the fixed-dose combination of 400 mg ibuprofen plus 100 mg caffeine for the treatment of acute headache.
急性頭痛治療のためのイブプロフェン400mgとカフェイン100mgの固定用量配合剤を調査した薬局ベースの観察研究における有効性と忍容性評価の相関 (機械翻訳の邦題)
記録の確認項目
- 研究デザイン
- その他の原著論文
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- 出版年
- 2023
- 出典
- doi.org
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- 有効な記録
- 状態確認日
- 2026/08/17
- 収集日
- 2026/08/03
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- 確認期限内
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- 自動処理
- 記録状態
- 公開
日本語要約(機械生成)
本研究は、ドイツの地域薬局で実施された観察研究の二次解析であり、市販の鎮痛薬(イブプロフェン400mg+カフェイン100mg)を購入した頭痛患者を対象に、痛みの軽減開始時間(OPR)、その評価(AOPR)、有効性・忍容性の評価、2時間後の疼痛強度などを調査し、これらの相関を分析した。その結果、OPRとAOPRの相関は高く(r=0.594)、15分以内の鎮痛開始は「非常に速い」、30分以内は「速い」と評価された。また、有効性評価と2時間後の疼痛強度変化率(%PID)の相関(r=0.487)、OPR/AOPRと%PID、忍容性評価、有効性評価の間にも有意な正の相関が認められた(r=0.206〜0.608)。さらに、過去の治療と比較して、89%以上の患者が本剤の鎮痛速度、有効性、忍容性を同等以上と評価した。これらの結果から、急性頭痛薬の有効性評価は、鎮痛開始時間や忍容性評価と強く関連することが示唆された。
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抄録
Introduction: Observational studies are valuable for investigating correlations between patient-reported treatment outcomes. In this study, we report a secondary analysis of a published pharmacy-based observational (patient-centered "real-world" outcomes) study on experiences reported by patients who treated their headache with an over-the-counter analgesic.Methods: A pharmacy-based exploratory survey was conducted in German community pharmacies. Patients buying a fixed-dose analgesic combination product (400 mg ibuprofen + 100 mg caffeine; IbuCaff) to treat their headache were offered a questionnaire that contained-among others-questions about time to onset of pain relief (OPR), assessment of time to onset of pain relief (AOPR), assessment of efficacy and tolerability, and pain intensity 2 h after intake. A correlation analysis of the data was performed. Moreover, perceived treatment effects compared to other acute headache medications used in the past were collected.Results: The correlation between OPR and AOPR was high (Spearman rank correlation r = 0.594, p < 0.0001). Headache patients assessed the onset of analgesic action within 15 min as "very fast" and within 30 min as "fast". The other readouts were correlated as well [assessment of efficacy and % pain intensity difference (%PID) at 2 h: r = 0.487; OPR/AOPR and %PID at 2 h: r = 0.295/0.318; OPR/AOPR and assessment of tolerability: r = 0.206/0.397; OPR/AOPR and assessment of efficacy: r = 0.406/0.594; assessment of efficacy and assessment of tolerability: r = 0.608; p < 0.0001 for all correlations]. Compared to previous treatments, most patients (>89%) assessed the speed of analgesic action, efficacy, and tolerability of IbuCaff as equal to or better than for the previous treatment.Discussion: Headache patients assessed the onset of analgesia within 15 min as "very fast" and within 30 min as "fast". Efficacy assessments for acute headache medication appear to be highly correlated.
DOI 10.3389/fneur.2023.1273846
PMID 37941578
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