Journals / Ege Klinikleri Tıp Dergisi / 2021 / Cilt: 59 - Sayı: 3

Evaluation of the Efficacy and Safety of D-Colefor (25-OH Vitamin D) Patients

D-Colefor (25-OH Vitamin D) Kullanmış Hastalarda Etkinlik ve Güvenliğinin Değerlendirilmesi

Pages
1–4
Publication Date
2022-10-11
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Results: It was determined that the use of the capsule form of oral vitamin D twice a week for eight weeks for 2x20000 IU increased serum vitamin D levels of 58.8% of the patients to the adequate dose of 30 ng/dl and above.

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: This study evaluates the vitamin D results inpatients diagnosed with vitamin D deficiency and used the oral vitamin D in capsule form twice a week for 2x20000UI during eight weeks (D-Colefor 14 capsules).
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Key Findings & Data:Material and Methods: Patients who were found to have vitamin D deficiency and whose vitamin D level was 20 ng/dl and below, who used oral vitamin D (D-Colefor capsule) 40000 IU per week (2X20000 IU for two days) for eight weeks and whose vitamin D measurement was made at the end of eight weeks were included in the study.
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Conclusion & Impact:Results: It was determined that the use of the capsule form of oral vitamin D twice a week for eight weeks for 2x20000 IU increased serum vitamin D levels of 58.8% of the patients to the adequate dose of 30 ng/dl and above.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objective: This study evaluates the vitamin D results inpatients diagnosed with vitamin D deficiency and used the oral vitamin D in capsule form twice a week for 2x20000UI during eight weeks (D-Colefor 14 capsules). Material and Methods: Patients who were found to have vitamin D deficiency and whose vitamin D level was 20 ng/dl and below, who used oral vitamin D (D-Colefor capsule) 40000 IU per week (2X20000 IU for two days) for eight weeks and whose vitamin D measurement was made at the end of eight weeks were included in the study. Our study was conducted retrospectively bys scanning patient files. We planned to investigate the treatment results by determining the percentage of patients whose vitamin D level exceeded 30 ng/dl, which was considered sufficient, after eight weeks. Results: It was determined that the use of the capsule form of oral vitamin D twice a week for eight weeks for 2x20000 IU increased serum vitamin D levels of 58.8% of the patients to the adequate dose of 30 ng/dl and above.

Özet

Amaç: D vitaminin eksikliği tanısı alan hastalarda, kullanıma giren kapsül formundaki oral D vitamini preparatını haftada iki gün 2x20000 UI 8 hafta (D-Colefor 14 kapsül) kullanmış hastaların D vitamini sonuçlarının değerlendirilmesi. Materyal ve Metod: D vitamin eksikliği tespit edilmiş olup D vitamin düzeyi 20 ng/dl ve altında olan oral D vitamini ( D-Colefor kapsül) tedavisini haftada 40000 IU(iki gün 2X20000 IU) 8 hafta kullanmış olan ve 8 hafta bitiminde D vitamin ölçümü yapılmış olan hastalar çalışmaya alınmıştır. Çalışmamız retrospektif olarak hasta dosyaları taranarak yapılmıştır. Sekiz hafta sonunda D vitamin düzeyinin yeterli olarak kabul edilen 30 ng/dl üzerine çıkan hasta sayılarının oranını belirleyerek tedavi sonuçlarını araştırmayı planladık. Sonuç: Oral D vitamininin kapsül formunun 8 hafta boyunca hafta da iki doz 2x20000 IU kullanımının serum D vitamin düzeylerini hastaların %58.8 ‘de yeterli doz olan 30 ng/dl ve üzerine yükselttiği saptanmıştır

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Cite This Article

DUMAN, G., SARIAKÇALI, B., TUNAHAN, H. (2022). Evaluation of the Efficacy and Safety of D-Colefor (25-OH Vitamin D) Patients. Ege Klinikleri Tıp Dergisi, Cilt: 59 - Sayı: 3, 1–4. https://ajindex.com/articles/495587

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