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18 B

Nat Rev Microbiol 2007,5(11):883–891.PubMedCrossRef

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2008; Stevens 2002) Items were assigned to a factor if their fac

2008; Stevens 2002). Items were assigned to a factor if their factor loading was 0.40 or greater (Stevens 2002). In case of cross-loadings, they were assigned to the factor with highest factor loading. The selection of items forming the definite subscale was based on the following considerations: 1. The content of the items: selected items should clearly represent the subconstruct

with as many different facets as possible.   2. Factor loading: items with higher factor loadings were preferred.   3. Cronbach’s alpha: items with highest contribution mTOR activity to the scale’s overall alpha were proposed for selection.   The analyses were repeated after each deletion of items until the unidimensional structure of each subscale was stable without

further improvement in the alpha coefficient. MM-102 clinical trial A Cronbach’s alpha of at least 0.70 was regarded sufficient and above 0.80 as good (Nunnally 1978; Streiner and Norman 2008). Since the item pool was too large (231 items) to analyze in one PCA, we analyzed four clusters of themes that are related to each other from a theoretical point of view. This division is in line with existing models of job performance (Viswevaran and Ones 2000). Our first cluster, “cognitive aspects of work functioning”, corresponds with the idea of task performance. The second cluster, “causing incidents”, corresponds with counterproductive behavior, although we do not regard causing incidents as voluntary, which is part of the definition of counterproductive behavior. Our third cluster, “interpersonal behavior”, and fourth cluster, “energy

and Metabolism inhibitor motivation”, are in accordance with organizational performance and the extra effort needed to perform the work, respectively. Meloxicam See Table 2 for the allocation of themes to the clusters. Finally, to test whether the selected subscale structure remained stable, a confirmatory factor analysis with all remaining items from all clusters was carried out, using the Oblique Multiple Group Method (Stuive et al. 2008; Stuive et al. 2009). Based on the highest item test correlations for each item on each subscale, it can be determined for which subscale the individual items have the best fit. Possible incorrect assignments of items to subtests were corrected in this step. All statistical analyses were performed using SPSS version 16.0, except for the Parallel Analysis, which was conducted using Monte Carlo PCA for Parallel Analysis (Watkins 2006). Results Results part 1: development of the item pool The literature reviews together with the five focus groups initially yielded 13 themes of impaired work functioning with underlying items. The themes resulting from the systematic literature review and the focus groups overlapped to a large extent. However, the focus group data provided more detailed themes on task execution and comprehensive examples of behavior for all themes.

5 months (standard deviation 4 0 months) The time between the fi

5 months (standard deviation 4.0 months). The time between the first and third QFT was, on average, 19.8 months (standard deviation 5.5 months). No association was observed between the time span of the QFTs and the probability of conversion or reversion in the QFT (data not shown). Nine HCWs were diagnosed with active TB, all but SBI-0206965 ic50 two were acid-fast bacillus (AFB)-positive, culturally confirmed cases. In one person, diagnosis was based solely on PCR (Table 6). All persons with active TB were positive in the first QFT. The TST was ≥15 mm in seven and 10–14 mm in two of them. Seven HCWs had

pulmonary TB, one pleural TB, and one skin TB. Six active TB cases were diagnosed within 2 months of the first QFT. The other three cases were diagnosed three, seven, and 19 months after the first positive QFT. In one case, a second QFT was performed at the time of diagnosis 3 months after the first QFT and an Belnacasan concentration increase from 0.51 to 1.96 IU/mL was observed. The median of the INF-γ concentration in those with actual Luminespib purchase pulmonary TB was 2.26 IU/mL, the minimum was 0.51 IU/mL, and the maximum 6.32 UI/mL. For the HCW with pleural TB the INF-γ in the first QFT was 0.42 IU/mL and in the skin TB case it was >10 IU/mL. After diagnosis and treatment,

a reversion occurred in the patient with pleural TB and a sharp decline occurred in the HCW with cutaneous TB (>10–1.04 IU/mL). Carteolol HCl For the other six cases, increases and decreases of INF-γ concentration were observed three times, respectively. A positive QFT led to diagnosis in four HCWs with no symptoms. In the other 5 HCWs with pulmonary, active TB, typical symptoms such as cough, fever, weakness, or weight loss were observed along with a positive QFT. Table 6 Characteristics of the 9 HCWs diagnosed with active TB TB Gender Age TST mm 1st QFT IU/mL Months between 1st QFT and diagnosis 2nd QFT IU/mL Symptoms at first QFT Pneumal Female 26 17 0.51 3 1.96* None Pneumal Female 39 18 3.97 <1 6.29 None Pneumal Female 25 16 6.32 19 1.30

Cough Pneumal Female 29 17 2.11 <1 3.28 Cough Pneumal Female 25 13 1.30 <1 1.22 Cough, fever Pneumal Female 31 22 0.92 7 0.56 Cough, weakness, weight loss Pneumal Female 25 14 2.41 <2 3.57 None Pleurala Male 26 20 0.42 <1 0.10 None Cutaneousb Female 50 21 >10 <1 1.04 Skin lesion * In all but the first case, the second QFTs were performed after diagnosis a Positive PCR, if not indicated otherwise all cases were AFB-positive and culturally confirmed bCulturally confirmed Discussion Our study is the largest follow-up study for serial testing to date. Furthermore, it is also the only study on serial testing that actually observed active TB cases, thus allowing conclusions about test interpretation in serial testing to be based on these findings.