Wednesday, December 19, 2012

癌因性疲憊症將有ICD疾病碼(Cancer-Related Fatigue, CRF)in ICD-10 !!


Cancer Related Fatigue   Author(s): Gary M Reisfield MD and George R Wilson MD  Background While several recent studies have found fatigue to be the single most prevalent, severe, and disabling symptom in cancer patients – exceeding even pain – it remains both underrecognized and poorly treated by physicians (1). This Fast Fact reviews diagnostic and treatment approaches in the palliative care setting.  Characteristics of Fatigue Cancer-related fatigue (CRF) is a persistent sense of tiredness/diminished energy related to cancer and/or its treatment, which is not relieved by rest, and which causes diminution in functional capacity and quality of life. Additional proposed ICD-10 features include: diminished concentration; diminished motivation; insomnia or hypersomnia; nonrestorative sleep; short-term memory deficits, and marked emotional reactivity to fatigue that are not primarily consequences of depression (2).  Causes   CRF is often multifactorial, with biochemical, physiological, psychological, and behavioral dimensions that remain poorly defined. Assessment is aimed at identifying correctable causes and determining the impact of CRF on both patients and caregivers. Common causes of CRF include:  Direct effect from cancer and/or treatments Sedating medications Deconditioning Psychiatric co-morbidities (e.g. depression, anxiety) Hypoxemia, or severe anemia (Hb ≤8 g/dL) and possibly moderate anemia (Hb ≤11g/dL) Systemic infection and/or or significant organ dysfunction (e.g. heart, liver, kidney, lung) Electrolyte abnormalities (e.g. Na+, K+, Mg++ , Ca++) Nutritional imbalance/impairment Sleep disturbance Uncontrolled pain  Specific Treatments   Treatment should be directed toward correcting identifiable causes, e.g. elimination of sedating drugs, correction of anemia or electrolyte imbalance.  NonSpecific Treatments Nonspecific treatments may be helpful in reducing fatigue, optimizing function, and promoting adaptation.   Education: Educate patient/family about CRF in order to normalize the symptom and promote adaptation/adjustment through setting realistic goals; modifying and prioritizing activities; and planning activities around diurnal variations in energy levels. Exercise: Several randomized controlled trials showed benefit of exercise in managing fatigue in patients undergoing active antineoplastic treatment (3). Aerobic exercise (low to moderate intensity; progressive) is ideal, but benefits may be realized with resistance training. A reasonable goal is 20-30 minutes of (cumulative) exercise per day, 4-5 days per week.Drug Therapy: There is little good data for non-specific drug therapy in CRF. The following drugs have been used with variable success: Psychostimulants: While there is a growing literature on the use of psychostimulants for CRF, there is a lack of good controlled trails. Methylphenidate: small studies have shown some efficacy in CRF, but a recent RCT of methylphenidate, 5 mg po q2h prn (maximum dose: 20 mg/d) showed no difference from placebo at one week (4). Start with 2.5-5 mg and titrate as necessary to 15-30 mg po at 08:00 and noon. Modafanil: pilot studies indicate efficacy in the treatment of fatigue associated with depression, MS, ALS, and HIV. Potentially fewer side effects than other psychostimulants. Start with 50 mg po qam and titrate as necessary to 200-400 mg po qam. Corticosteroids: These may provide a modest duration of benefit (2-4 weeks) offset by the potential for significant toxicity. Reported regimens have included prednisone 7.5-10 mg po qd; dexamethasone 1-2 mg po qd; methylprednisolone 32 mg po qd. Megestrol acetate: Two double-blind, crossover studies showed reduction in CRF with doses of 160 mg po tid (5,6).


References  

nMorrow GR, Shelke AR, Roscoe JA. Management of cancer-related fatigue. Cancer Investigation. 2005; 23:229-239. Fatigue PDQ. National Cancer Institute. Available at: www.cancer.gov/cancertopics/pdq/supportivecare/fatigue.

n Mock V. Evidence-based treatment of cancer-related fatigue. J Natl Cancer Inst Monogr. 2004; 32:112-118.

nBruera E, Valero V, Driver L, et al. Patient-controlled methylphenidate for cancer fatigue: a double-blind, randomized, placebo-controlled trial. J Clin Oncol. 2006; 24:2073-2078.

nBruera E, Macmillan K, Hanson J, et al. A controlled trial of megestrol acetate on appetite, caloric intake, nutritional status, and other symptoms in patients with advanced cancer. Cancer. 1990; 66:1279-1282.

nBruera E, Ernst S, Hagen N, et al. Effectiveness of megestrol acetate in patients with advanced cancer: a randomized, double-blind, crossover study. Cancer Prev Control 1998; 2:74-78.

nFast Facts and Concepts are edited by Drew A Rosielle MD, Palliative Care Center, Medical College of Wisconsin. For more information write to: drosiell@mcw.edu. More information, as well as the complete set of Fast Facts, are available at EPERC: www.eperc.mcw.edu.  

nVersion History: This Fast Fact was originally edited by David E Weissman MD and published in January 2007. Current version re-copy-edited in April 2009.  

nCopyright/Referencing Information: Users are free to download and distribute Fast Facts for educational purposes only. Reisfield GM, Wilson GR. Cancer-Related Fatigue. Fast Facts and Concepts. January 2007; 173. Available at: http://www.eperc.mcw.edu/fastfact/ff_173.htm.  

nDisclaimer: Fast Facts and Concepts provide educational information. This information is not medical advice. Health care providers should exercise their own independent clinical judgment. Some Fast Facts cite the use of a product in a dosage, for an indication, or in a manner other than that recommended in the product labeling. Accordingly, the official prescribing information should be consulted before any such product is used.  

 

ACGME Competencies: Medical Knowledge, Patient Care  Keyword(s): Non-Pain Symptoms and Syndromes  

 

懷特新藥申請健保核價 明年Q1可望過關 自由時報-20121220 上午05:00 〔自由時報記者陳永吉/台北報導〕行政院正研議給予國內自行研發完成的新藥健保核價,估計相關辦法會在年底完成,懷特(4108)研發的「懷特血寶」主要是針對癌末病人的「癌因性疲憊症」進行治療,上個月底已經正式遞件申請健保核價,昨天懷特董事長李成家說,應該明年第一季就能核准,因此明年公司營運將比今年好。李成家表示,懷特血寶現為處分藥,是由美吾華銷售團隊在北中南各大醫院進行推廣,由於沒有健保核價,每針需自費12650元,如果能取得健保核價,希望能減少病人負擔。懷特總經理黃中洋則指出,現在全台灣約有5萬名癌末病患,許多癌末病患因為化療、放療都極為痛苦,過去癌因性疲憊症因為不是疾病的一種,所以醫生無法開立處方,但根據ICD(國際疾病傷害及死因分類標準)明年最新的第十個版本,已將癌因性疲憊症列為疾病的一種,未來相關病患就有處方藥可以使用。黃中洋表示,懷特血寶4月拿到藥證後,銷售一季優於一季,且當時各大醫院主要採購藥品時間已過,只能用臨時採購來購買,所以數量不多,但明年血寶將有機會列為各醫院採購的藥品選項,如果又能獲得健保核價,相信銷售能更上一層樓。由於懷特還有多項新藥持續研發中,仍在燒錢階段,因此李成家對明年懷特能否轉虧為盈,沒有太大把握,但李成家表示,近期完成增資後,取得12億元資金,除了繼續研發新藥外,也會添購新廠房,會以既有且符合PIC/S規範的整廠為優先考慮,合併也是選項之一,將可增加懷特未來的營運動能。

 

台灣44家PIC/S GMP認證藥廠!!


國際授證-領先日、韓 我明年起加入 醫藥品稽查協約組織2012-12-19 中國時報 邱俐穎/台北報導國內藥品實施GMP屆滿30周年,衛生署食品藥物管理局昨舉辦研討會,並宣布台灣領先日本、南韓,明年11起正式成為國際「醫藥品稽查協約組織」(PIC/S)第43個會員。國內自民國71年起實施藥品GMP管理制度,歷經2年半努力終於在今年10月成功叩關。衛生署長邱文達表示,正式成為PIC/S43個會員,是衛生署藥政管理上的重要里程碑。邱文達指出,目前國內藥品用量7成來自學名藥,獲得國際PIC/S GMP認證的藥廠所生產的學名藥,相對於同成分的原廠藥,具備相同品質與藥效,讓醫療資源能夠更廣泛、有效的運用在民眾身上。邱文達說,目前國內已有44家通過PIC/S GMP認證,預計在民國103年底前全面完成PIC/S GMPPIC/S主席代表瑞薇絲(Dr. Vasiliki Gerogia Revithi)昨正式授予食品藥物管理局長康照洲PIC/S入會證書。

 

國衛院長 龔行健出任

 中央社2012-12-20 09:56 AM (中央社記者龍瑞雲台北20日電)國家衛生研究院今天表示,經國衛院董事會決議與行政院同意,由中央研究院院士龔行健擔任第五任院長,明天就任。 國衛院指出,前院長伍焜玉831卸任院長職務後,由副院長王陸海代理職務。國衛院表示,為辦理新任院長遴選作業,國衛院董事會成立院長遴選委員會,負責在國內外徵才評選後向董事會舉薦候選人任務,最後經董事會與候選人逐一面談後,由龔行健脫穎而出。龔行健自台灣大學化學系畢業後,赴美國加州理工學院攻讀化學博士學位,並在美國加州大學舊金山分校醫學院進行博士後研究。國衛院指出,龔行健研究領域主要是腫瘤病毒學及癌症生物學,且在反轉錄病毒、皰疹病毒以及原癌基因研究上有重大發現。多年來研究成果豐碩,共有200餘篇創新研究論文發表在國際雜誌,並於1998年當選中央研究院院士,是享譽國際知名學者,學術成就與聲望獲國際肯定。國衛院說,龔行健熟悉國內相關醫藥衛生發展。近幾年回國擔任台北醫學大學轉譯醫學綜合實驗室特聘講座教授及國立清華大學生命科學院特聘講座教授,對國內醫藥衛生研究有深刻的認識。1011220

 

資誠聯合 多年成功佈局生技事業群 !


浩鼎(4174) 本公司更換會計師事務所及簽證會計師發言時間 101/12/1918:27:03發言人 許友恭 發言人職稱 執行長 發言人電話 (02)2655-8799 主旨 : 本公司更換會計師事務所及簽證會計師符合條款第7款事實發生日101/12/19說明 1.董事會通過日期(事實發生日):101/12/192.舊會計師事務所名稱:安永聯合會計事務所3.舊任簽證會計師姓名1:蕭翠慧會計師4.舊任簽證會計師姓名2:曾祥裕會計師5.新會計師事務所名稱:資誠聯合會計事務所6.新任簽證會計師姓名1:曾惠瑾會計師7.新任簽證會計師姓名2:張明輝會計師8.變更會計師之原因:本公司因考量業務發展及管理需求,更換會計師事務所9.說明係由公司主動終止委任或不再繼續委任或前任會計師主動終止委任或不再繼續接受委任:公司主動終止委任10.公司通知或接獲通知終止之日期:101/12/2011.最近二年度已申報或即將編製之財務報告是否曾經會計師調整或提出內部控制重大改進事項之建議:12.公司對上開調整或建議事項有無不同意見(若有不同意見,請詳細說明每一事項之性質、公司原處理方法與最後處理結果暨繼任會計師對各該事項之書面意見):不適用13.公司正式委任繼任會計師前,是否曾就上開前任會計師所做調整及建議事項之處理及其對財務報表可能簽發之意見,諮詢該會計師(若有,請輸入詢問事項及結果):不適用14.說明是否授權前任會計師對繼任會計師所提合理之詢問(包括上開所述不同意見之情事)充分回答:15.其他應敘明事項:無以上資料均由各公司依發言當時所屬市場別之規定申報後,由本系統對外公佈,資料如有虛偽不實,均由該公司負責.

 

台微體ProDex 積極尋找新臨床適應症 !!


台微體 雙題材帶旺行情【經濟日報╱記者黃文奇/台北報導】 2012.12.20 03:37 am 新藥股年底掛牌潮還有一波,帶動行情續旺!興櫃股王台微體(4152)將在明(21)日以158元掛牌上櫃。台微體過去已有4項新藥成功授權,法人透露,明年仍將有3項新藥完成授權。台微體昨日興櫃參考價收收272.5元,受到掛牌前暖身運動激勵,昨日上漲31.52元動能最強。除了台微體之外,另受惠新藥公司掛牌潮持續帶動,醣聯、基亞、智擎等各擁授權、併購題材,動能繼續攀高。台微體至今已完成4項授權案,公司透露,目前還有3項藥物正在規劃授權,並已經有洽談對象。法人透露,台微體明年有機會授權的項目,包括治療全身性黴菌的安畢黴(AmBiL)、抗老年黃斑部病變的ProDex,後者預計明年將於台、美兩地提出新藥臨床試驗審查申請(IND),並將從臨床12期同步進行。另外,第3項正待授權中的藥物,還有多重機制抗癌新藥「立普帝康」(Lipotecan),已獲歐盟及美國認可為孤兒藥,也入選為首批加入「兩岸藥品研發合作專案試辦計畫」指標案。台微體為永豐餘集團轉投資新藥研發公司,承銷價格為158元,較目前的興櫃價格明顯偏低,而其新藥授權金將在明年陸續大筆認列,因此具有想像空間。此外甫掛牌上櫃的醣聯,連兩日演出蜜月行情,醣聯和台微體同為新藥研發公司,又都有授權金題材加持,因此讓比價行情續攀。醣聯精於醣質領域研究,2009年以治療大腸癌的GNX8進度最快,授權給日本大塚製藥,總授權額度達1.96億美元(約新台幣57億元);推估今年在GXN順利進入臨床後,醣聯即可認列300萬美元的里程碑金。另外,智擎、基亞近期也頗受矚目,智擎2011年以2.2億美元高額授權金,將旗下抗胰臟癌新藥PEP022.2億美元的高架授權給美商梅里馬克,明年上半年也可望有大筆階段里程碑進帳。近期,也吸引電子大廠群光投資智擎近3.5億元。基亞銷售上海子公司浩源的題材繼續發酵,近期基亞將持有70.5%股權的上海核酸檢驗公司浩源,售予美商珀金埃爾默,總價款6,800萬美元,今年第4季已認列4.6億元,每股稅後純益貢獻3.84元,今年確定轉盈。展望明年,基亞還將陸續認列後續簽約款,及未來3年的3,000萬美元里程碑金,備受矚目。【2012/12/20 經濟日報】

 

 

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