Struggles and successes: experiences of a beta test site.

More than 400 hospitals participated in the first stages of beta testing for Joint Commission-developed indicators. One hospital chosen as a beta test site describes how this experience led to an evaluation of its own performance.

Automated phase sensing and control of an external Talbot cavity laser with phase-contrast imaging.

We describe a novel phase-sensing and control system, based on phase-contrast imaging, operating within a linear external cavity laser consisting of 18 GaAlAs edge-emitting gain stripes. The system is used to achieve single-spatial-mode operation and diffraction-limited output from the linear cavity, which uses diffractive coupling at a Talbot plane to achieve coherent operation.

Intracavity phase correction of an external Talbot cavity laser with the use of liquid crystals.

Arrays of GaAlAs emitters have been diffractively coupled by using an external Talbot cavity to support a single spatial mode; however, element-to-element phase differences distort the desired spatial mode. To enable element-to-element phase correction, we incorporated a 20-element array of tunable liquid-crystal phase shifters into a 20-element GaAlAs external Talbot cavity laser. Using the tunable phase shifters, we corrected spatial mode distortions, which resulted in 663 mW of nearly diffraction-limited power.

Distinguishing characteristics of a new neuroblastoma cell line.

The characteristics of a new neuroblastoma cell line (MC-NB-1) established from the bone marrow of a 2-year-old male are described. Morphologically, the cells appear as flattened and epithelial-like or as small and spherical. Electron microscopy demonstrated microtubules and dense core secretory granules. The doubling time was approximately 35 hr. Isoenzyme patterns and catecholamine secretion indicated a human line of neuronal origin. The soft agar tumor colony forming system demonstrated drug resistance in vitro comparable to in vivo nonresponsiveness. The stemline karyotype of MC-NB-1 is 44,Y,del(1) (p22:), -4, -7, +del(7)(q22:), -16, +t(7;16)(16pter leads to 16q24::7q22 leads to 7q32), -17. Additionally, double-minute bodies were observed. However, no evidence of homogeneous staining regions (HSRs) were detected.

In vitro enhancement of peripheral blood mononuclear cell natural killer activity following short term incubation with fetal calf serum.

This study demonstrates that short term incubation of blood mononuclear cells (MC) in heterologous sera enhances their natural killer (NK) but not their antibody dependent killer (K) activity, and confirms that NK stimulation is not related to blastogenesis. MC were obtained from healthy donors and incubated with RPMI 1640 supplemented with various serum sources. NK and K activity of incubated vs. fresh MC against SK-N-SH, Chang or Raji cell line targets were compared in a 4-hr 51Cr release assay. A significant (p less 0.01) increase in NK cytotoxicity was detected when MC were incubated with fetal calf serum (FCS) or human AB serum (ABS) at 37 degrees C. When a more sensitive NK target cell (K-562) was used only the cells incubated in FCS demonstrated increased NK cytotoxicity. Augmentation of NK cell activity by FCS was not related to blastogenesis, mitosis, natural antibodies against lymphocytes or target cells, immunoglobulin complexes or alterations in MC OKT4 and OKT8 subpopulations. In contrast to NK activity, K cytotoxicity was not increased after incubation at 37 degrees C in FCS or ABS, and it was depressed in IPT (p less than 0.05). Thus FCS is capable of stimulating NK cell activity against human tumor cell lines in less in less than 24 hr.