67 research outputs found

    p53 Expression in Pretreatment Specimen Predicts Response to Neoadjuvant Chemotherapy Including Anthracycline and Taxane in Patients with Primary Breast Cancer.

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    While clinical and pathologic responses are important prognostic parameters, biological markers from core needle biopsy (CNB) are needed to predict neoadjuvant chemotherapy (NAC) response, to individualize treatment, and to achieve maximal efficacy. We retrospectively evaluated the cases of 183 patients with primary breast cancer who underwent surgery after NAC (anthracycline and taxane) at the National Cancer Center Hospital (NCCH). We analyzed EGFR, HER2, and p53 expression and common clinicopathological features from the CNB and surgical specimens of these patients. These biological markers were compared between sensitive patients (pathological complete response;pCR) and insensitive patients (clinical no change;cNC and clinical progressinve disease;cPD). In a comparison between the 9 (5%) sensitive patients and 30 (16%) insensitive patients, overexpression of p53 but not overexpression of either HER2 or EGFR was associated with a good response to NAC. p53 (p0.045) and histological grade 3 (p0.011) were important and significant predictors of the response to NAC. The correspondence rates for histological type, histological grade 3, ER, PgR, HER2, p53, and EGFR in insensitive patients between CNB and surgical specimens were 70%, 73%, 67%, 70%, 80%, 93%, and 73%. The pathologic response was significantly associated with p53 expression and histological grade 3. The correspondence rate of p53 expression between CNB and surgical specimens was higher than that of other factors. We conclude that the level of p53 expression in the CNB was an effective and reliable predictor of treatment response to NAC

    Epidemiology of potentially inappropriate medication use in elderly patients in Japanese acute care hospitals.

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    [Purpose]The elderly receive many medications which may have adverse effects. Little evidence is available about the epidemiology of potentially inappropriate medications being prescribed to the elderly in Japan as defined by the Beers criteria, or whether or not these medications result in harm when used in this population. [Methods]We conducted a prospective cohort study of patients aged ≄65 years who were admitted to three acute care hospitals in Japan. Trained research nurses followed up patients from randomly selected wards and collected data about their medications and all potential adverse drug events (ADEs). Two independent reviewers evaluated all the data. The use of potentially inappropriate medications and their effects on patients were identified using the updated Beers criteria. [Results]A total of 2155 elderly patients were eligible; 56.1% received at least one drug listed in the Beers criteria (BL drug). The rates of BL drug prescriptions were 103.8 per 100 admissions and 53.7 per 1000 patient-days, and the incidence rate of ADEs related to BL drugs was 1.7 per 100 BL drug prescriptions. Among patients aged ≄65 years, relatively younger patients (p = 0.0002) and those with less complications (p = 0.04) were likely to be prescribed BL drugs. [Conclusions]Although BL drugs were frequently prescribed to elderly Japanese inpatients, the incidence of related ADEs appeared infrequent. These data suggest that re-evaluation of the appropriateness of the Beers criteria is needed before they are used in Japan and other nations to assess quality or for decision support

    Coincidence analysis to search for inspiraling compact binaries using TAMA300 and LISM data

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    Japanese laser interferometric gravitational wave detectors, TAMA300 and LISM, performed a coincident observation during 2001. We perform a coincidence analysis to search for inspiraling compact binaries. The length of data used for the coincidence analysis is 275 hours when both TAMA300 and LISM detectors are operated simultaneously. TAMA300 and LISM data are analyzed by matched filtering, and candidates for gravitational wave events are obtained. If there is a true gravitational wave signal, it should appear in both data of detectors with consistent waveforms characterized by masses of stars, amplitude of the signal, the coalescence time and so on. We introduce a set of coincidence conditions of the parameters, and search for coincident events. This procedure reduces the number of fake events considerably, by a factor ∌10−4\sim 10^{-4} compared with the number of fake events in single detector analysis. We find that the number of events after imposing the coincidence conditions is consistent with the number of accidental coincidences produced purely by noise. We thus find no evidence of gravitational wave signals. We obtain an upper limit of 0.046 /hours (CL =90= 90 %) to the Galactic event rate within 1kpc from the Earth. The method used in this paper can be applied straightforwardly to the case of coincidence observations with more than two detectors with arbitrary arm directions.Comment: 28 pages, 17 figures, Replaced with the version to be published in Physical Review

    Results of the search for inspiraling compact star binaries from TAMA300's observation in 2000-2004

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    We analyze the data of TAMA300 detector to search for gravitational waves from inspiraling compact star binaries with masses of the component stars in the range 1-3Msolar. In this analysis, 2705 hours of data, taken during the years 2000-2004, are used for the event search. We combine the results of different observation runs, and obtained a single upper limit on the rate of the coalescence of compact binaries in our Galaxy of 20 per year at a 90% confidence level. In this upper limit, the effect of various systematic errors such like the uncertainty of the background estimation and the calibration of the detector's sensitivity are included.Comment: 8 pages, 4 Postscript figures, uses revtex4.sty The author list was correcte

    Observation results by the TAMA300 detector on gravitational wave bursts from stellar-core collapses

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    We present data-analysis schemes and results of observations with the TAMA300 gravitational-wave detector, targeting burst signals from stellar-core collapse events. In analyses for burst gravitational waves, the detection and fake-reduction schemes are different from well-investigated ones for a chirp-wave analysis, because precise waveform templates are not available. We used an excess-power filter for the extraction of gravitational-wave candidates, and developed two methods for the reduction of fake events caused by non-stationary noises of the detector. These analysis schemes were applied to real data from the TAMA300 interferometric gravitational wave detector. As a result, fake events were reduced by a factor of about 1000 in the best cases. The resultant event candidates were interpreted from an astronomical viewpoint. We set an upper limit of 2.2x10^3 events/sec on the burst gravitational-wave event rate in our Galaxy with a confidence level of 90%. This work sets a milestone and prospects on the search for burst gravitational waves, by establishing an analysis scheme for the observation data from an interferometric gravitational wave detector

    タンキ ăƒ€ă‚€ă‚Źă‚Ż ăƒ„ă‚Šă‚·ăƒłă‚»ă‚€ ă‚«ăƒ†ă‚€ ïŒ’ăƒăƒłă‚»ă‚€ ノ わクセむ ガ ă‚·ăƒ„ă‚Šă‚źăƒ§ă‚Š ă‚čル ă‚·ă‚»ăƒ„ ニ ă‚Șă‚±ăƒ« ăƒ’ăƒ€ăƒȘ ハット ă‚żă‚€ă‚±ăƒł ノ ă‚žăƒƒă‚żă‚€ ăƒăƒ§ă‚Šă‚”

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    盼的:æœŹć­Šé€šäżĄćˆ¶èȘČçš‹ăźć­Šç”ŸăŒć°±æ„­ă™ă‚‹æ–œèš­ă§äœ“éš“ă™ă‚‹ăƒ’ăƒ€ăƒȘăƒ»ăƒăƒƒăƒˆäș‹äŸ‹ă‚’ć…šć›œ300ćșŠä»„äžŠăźç—…é™ąăšæŻ”èŒƒă—ç‰čćŸŽă‚’æ˜Žă‚‰ă‹ă«ă—ă€äș‹æ•…ć ±ć‘Šăźă—ăăżă‚„æ„è­˜ă«ă€ă„ăŠăźćźŸæ…‹ă‚’çŸ„る。æ–čæł•:ćŻŸè±ĄăŻ1ćčŽæŹĄç”Ÿ188損。2013ćčŽèłȘ敏箙èȘżæŸ»ă‚’ćźŸæ–œă€‚èȘżæŸ»ć†…ćźčăŻèƒŒæ™Żă€äș‹æ•…ć ±ć‘Šăźă—ăăżă€æ„è­˜ă€ăƒ’ăƒ€ăƒȘăƒ»ăƒăƒƒăƒˆäœ“éš“ă§ă€ć°è±Ąçš„ăȘäœ“éš“ă‚„æ°—æŒăĄăŻè‡Șç”±èš˜èŒ‰ăšă—ăŸă€‚ç”æžœ:曞揎率52%ă€‚ć°±æ„­ă™ă‚‹æ–œèš­ăŻ200ćșŠä»„äž‹ăźç—…é™ąă€æ–œèš­ăŒçŽ„7ć‰Čă‚’ć ă‚ăŸă€‚ăƒ’ăƒ€ăƒȘăƒ»ăƒăƒƒăƒˆäœ“éš“ăŻă€Œç™‚é€ŠäžŠăźäž–è©±ă€ă§ă€ç†±ć‚·ăƒ»æšŽćŠ›ăƒ»èȘ€ćš„ăƒ»ć…„æ”Žăƒ»é›ąé™ąă€ă€ŒèŠłćŻŸæƒ…ć ±ă€ăŒé«˜çŽ‡ă§ă€è‡Șç”±èš˜èŒ‰ă‹ă‚‰ăŻæłšć°„ăƒ»äžŽè–Źăƒ»è»ąć€’è»ąèœăŒäžŠäœă‚’ć ă‚ăŸă€‚äș‹æ•…栱摊た仕甄みは玄90%ăŒäżæœ‰ă—ă€æ„è­˜ă§ăŻçŽ„30%ăŒć ±ć‘Šă«æ¶ˆæ„”çš„ă§ă‚ăŁăŸă€‚ç”è«–:ć­Šç”ŸăŒć°±æ„­ă™ă‚‹æ–œèš­ă§ăźăƒ’ăƒ€ăƒȘăƒ»ăƒăƒƒăƒˆäœ“éš“ăźç‰čćŸŽăŻă€ç™‚é€ŠäžŠăźäž–è©±ăšćŒ»ćž«ă€æ‚Łè€…ăƒ»ćź¶æ—ă«é–ąă™ă‚‹é …ç›źăŒć…šć›œèȘżæŸ»ă‚ˆă‚Šé«˜ă„æŻ”çŽ‡ă‚’ć ă‚ăŸă€‚äș‹æ•…ć ±ć‘Šăźă—ăăżăŻæœ‰ă‚‹ă‚‚ăźăźé‹ç”šćźŸæ…‹ă‚„äș‹æ•…ć ±ć‘Šăźæ„è­˜ăźè§Łæ˜ŽăŻä»ŠćŸŒăźèȘČ題である。Objective: To reveal characteristics and perception of near-miss errors and its reporting system of hospitals where the students are employed, comparing with a national data of larger scale hospitals over 300 beds.Methods: A questionnaire survey was conducted in 2013 on 188 first-year working students in a correspondence course. Main question items were consisted of the background information, experience, perception, and the system of reporting near-miss errors. Significant events were asked in the form of an open question. Results: The response rate was 52%. Around 70% of the hospitals had less than 200 beds. There was an increase of the near-miss errors of burns, violence, aspirations, bathing, leaving hospitals, and observation on patient care. Also, increased cases at injection, medication, and falls were observed in open questions. Ninety percent of the facilities had a system of reporting near-miss cases but 30% of nurses were passive about the reporting. Conclusion:Features of near-miss errors at targeted hospitals were revealed as there were increased cases at patient care, and items related to doctors, patients or their families. Although most facilities have the system of incident report, analysis of the perception on near-miss errors and actual implementation of the system is further needed

    Why Are Outcomes Different for Registry Patients Enrolled Prospectively and Retrospectively? Insights from the Global Anticoagulant Registry in the FIELD-Atrial Fibrillation (GARFIELD-AF).

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    Background: Retrospective and prospective observational studies are designed to reflect real-world evidence on clinical practice, but can yield conflicting results. The GARFIELD-AF Registry includes both methods of enrolment and allows analysis of differences in patient characteristics and outcomes that may result. Methods and Results: Patients with atrial fibrillation (AF) and ≄1 risk factor for stroke at diagnosis of AF were recruited either retrospectively (n = 5069) or prospectively (n = 5501) from 19 countries and then followed prospectively. The retrospectively enrolled cohort comprised patients with established AF (for a least 6, and up to 24 months before enrolment), who were identified retrospectively (and baseline and partial follow-up data were collected from the emedical records) and then followed prospectively between 0-18 months (such that the total time of follow-up was 24 months; data collection Dec-2009 and Oct-2010). In the prospectively enrolled cohort, patients with newly diagnosed AF (≀6 weeks after diagnosis) were recruited between Mar-2010 and Oct-2011 and were followed for 24 months after enrolment. Differences between the cohorts were observed in clinical characteristics, including type of AF, stroke prevention strategies, and event rates. More patients in the retrospectively identified cohort received vitamin K antagonists (62.1% vs. 53.2%) and fewer received non-vitamin K oral anticoagulants (1.8% vs . 4.2%). All-cause mortality rates per 100 person-years during the prospective follow-up (starting the first study visit up to 1 year) were significantly lower in the retrospective than prospectively identified cohort (3.04 [95% CI 2.51 to 3.67] vs . 4.05 [95% CI 3.53 to 4.63]; p = 0.016). Conclusions: Interpretations of data from registries that aim to evaluate the characteristics and outcomes of patients with AF must take account of differences in registry design and the impact of recall bias and survivorship bias that is incurred with retrospective enrolment. Clinical Trial Registration: - URL: http://www.clinicaltrials.gov . Unique identifier for GARFIELD-AF (NCT01090362)

    Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry.

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    BACKGROUND: The Global Anticoagulant Registry in the FIELD-Atrial Fibrillation (GARFIELD-AF) is an ongoing prospective noninterventional registry, which is providing important information on the baseline characteristics, treatment patterns, and 1-year outcomes in patients with newly diagnosed non-valvular atrial fibrillation (NVAF). This report describes data from Indian patients recruited in this registry. METHODS AND RESULTS: A total of 52,014 patients with newly diagnosed AF were enrolled globally; of these, 1388 patients were recruited from 26 sites within India (2012-2016). In India, the mean age was 65.8 years at diagnosis of NVAF. Hypertension was the most prevalent risk factor for AF, present in 68.5% of patients from India and in 76.3% of patients globally (P < 0.001). Diabetes and coronary artery disease (CAD) were prevalent in 36.2% and 28.1% of patients as compared with global prevalence of 22.2% and 21.6%, respectively (P < 0.001 for both). Antiplatelet therapy was the most common antithrombotic treatment in India. With increasing stroke risk, however, patients were more likely to receive oral anticoagulant therapy [mainly vitamin K antagonist (VKA)], but average international normalized ratio (INR) was lower among Indian patients [median INR value 1.6 (interquartile range {IQR}: 1.3-2.3) versus 2.3 (IQR 1.8-2.8) (P < 0.001)]. Compared with other countries, patients from India had markedly higher rates of all-cause mortality [7.68 per 100 person-years (95% confidence interval 6.32-9.35) vs 4.34 (4.16-4.53), P < 0.0001], while rates of stroke/systemic embolism and major bleeding were lower after 1 year of follow-up. CONCLUSION: Compared to previously published registries from India, the GARFIELD-AF registry describes clinical profiles and outcomes in Indian patients with AF of a different etiology. The registry data show that compared to the rest of the world, Indian AF patients are younger in age and have more diabetes and CAD. Patients with a higher stroke risk are more likely to receive anticoagulation therapy with VKA but are underdosed compared with the global average in the GARFIELD-AF. CLINICAL TRIAL REGISTRATION-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01090362
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