高血壓 高尿酸 慢性腎病 胰島素 https://2019medicinenote.blogspot.com/2019/12/blog-post_57.html . 糖尿病相關筆記~目錄 https://2019medicinenote.blogspot.com/2020/01/blog-post_4.html

2019年12月17日 星期二

野外與登山醫學--- 高海拔肺水腫HAPE的藥物治療

非藥物治療包括下降, 給氧氣.

藥物治療包括:
Nifedipine: 可作為氧氣和下降的輔助治療. 或沒有氧氣也無法下降的輔助治療. 但實驗證據不夠多.
Tadalafil/sildenafil:
dexamethasone: 學理上有效但沒有臨床試驗證實, 目前建議用於合併AMS/HACE的 HAPE病患
beta agonist: 也許有效但沒有臨床試驗證實
無效的藥物包括: 其他利尿劑, 硝化甘油, 嗎啡.

Pharmacologic interventions — A summary of medications used to treat HAPE is provided (table 4). More thorough discussions of these treatments are found below.
Nifedipine — In the field setting, oxygen and descent remain the most important treatments for HAPE. Nifedipine may be considered adjunctive therapy when oxygen is unavailable and descent is difficult or impossible, although little clinical evidence supports the practice. (See 'General approach to treatment' above.)
Nifedipine is a nonspecific calcium channel blocker that acts by reducing pulmonary vascular resistance and PA pressure, as well as systemic resistance and blood pressure. It also slightly improves PaO2.
Recommended dosages vary, but a common regimen is to give 30 mg of a slow release formulation every 12 hours. Nifedipine is well tolerated by most patients and is unlikely to cause significant hypotension in previously healthy persons. Clinicians should give or be prepared to give isotonic intravenous fluid (eg, normal saline) to any critically ill HAPE patient who may be intravascularly depleted and is receiving nifedipine.
One unblinded uncontrolled study of six patients with HAPE found that nifedipine treatment led to clinical improvement [40]. However, another observational study involving 133 patients with HAPE reported that nifedipine offered no advantage when used as an adjunct to oxygen and descent [30].
Tadalafil and sildenafil — Tadalafil and sildenafil are phosphodiesterase-5 (PDE-5) inhibitors that augment the pulmonary vasodilatory effects of nitric oxide by blocking the degradation of cyclic guanosine monophosphate (cGMP), the intracellular mediator of nitric oxide. Nitric oxide is a potent pulmonary vasodilator and reduces hypoxic pulmonary vasoconstriction (HPV) and pulmonary hypertension in HAPE [5]. Both tadalafil and sildenafil have been shown to be effective as prophylaxis for HAPE, but neither has been studied as treatment [41-43]. (See 'Prophylactic medications' below.)
Nevertheless, based upon their mechanism of action, both tadalafil and sildenafil may be effective adjunct treatments for established HAPE when neither oxygen nor descent is an available option. These drugs may have advantages over nifedipine because they lower PA pressure with less risk of lowering systemic blood pressure. The appropriate dose for treatment is unknown but might be similar to that used for prophylaxis (tadalafil 10 mg by mouth every 12 hours; sildenafil 50 mg by mouth every eight hours).
Dexamethasone — Although glucocorticoids may have a role in prophylaxis, they have not been studied as treatment for HAPE. We reserve glucocorticoids for treatment of high altitude cerebral edema or severe acute mountain sickness, which may co-exist with HAPE. (See 'Prophylactic medications' below.)
Beta agonist — Salmeterol may be useful in the treatment of HAPE, but this remains unstudied. (See 'Prophylactic medications' below.)
Ineffective or contraindicated therapies — Diuretic therapy, nitrates, and morphine are no longer recommended in the treatment of HAPE and could be harmful.

預防急性痛風發作

Prophylaxis for acute gout flares after initiation of urate-lowering therapy 

Rheumatology, Volume 53, Issue 11, November 2014, Pages 1920–1926,
https://academic.oup.com/rheumatology/article/53/11/1920/1792549

當開始降尿酸藥物治療之後, 如何預防痛風急性發作
有兩種第一線治療, 可以使用六個月
1. 低劑量秋水仙素 colchicine 0.5 mg qd or BID
2. 低劑量消炎止痛藥物 NSAID naproxen 250 mg bid.
如果因任何原因無法使用上述兩種藥物治療. 可考慮低劑量類固醇
prednisone 或 prednisolone.
近期還有其他研究, 在服用 allopurinol 期間, 使用介白素抑制劑 IL-1 inhibitor 輔助治療
canakinumab
rilonacept


Abstract
This review summarizes evidence relating to prophylaxis for gout flares after the initiation of urate-lowering therapy (ULT). We searched MEDLINE via PubMed for articles published in English from 1963 to 2013 using MEsH terms covering all aspects of prophylaxis for flares. Dispersion of monosodium urate crystals during the initial phase of deposit dissolution with ULT exposes the patient to an increased rate of acute flares that could contribute to poor treatment adherence. Slow titration of ULT might decrease the risk of flares. According to the most recent international recommendation, the two first-line options for prophylaxis are low-dose colchicine (0.5 mg once or twice a day) or low-dose NSAIDs such as naproxen 250 mg orally twice a day. They can be given for up to 6 months. If these drugs are contraindicated, not tolerated or ineffective, low-dose corticosteroids (prednisone or prednisolone) might be used. Recently, reports for four trials described the efficacy of canakinumab and rilonacept, two IL-1 inhibitors, for preventing flares during the initiation of allopurinol therapy. Prophylaxis for flares induced by ULT is an important consideration in gout management. Low-dose colchicine and low-dose NSAIDs are the recommended first-line therapies. Although no IL-1 blockers are approved as prophylactic treatment, this class of drug could become an interesting option for patients with gout with intolerance or contraindication to colchicine, NSAIDs or corticosteroids.

秒懂家醫科-血糖血脂(膽固醇)

2025-07-02 11:48AM 【門診醫學】 2024年美國糖尿病學會指引 【門診醫學】高膽固醇血症的治療建議 【預防醫學:什麼食物會升高膽固醇?】