Echo Doppler parameters predict response to cardiac resynchronization therapy

Background  Cardiac resynchronization therapy (CRT) has been shown to reduce heart failure related morbidity and mortality. However, approximately 30% of patients do not respond to CRT. We investigated the usefulness of Echo Doppler parameters to predict reverse remodelling, functional improvement and mortality following CRT.
Materials and methods  Our population consists of 200 consecutive heart failure patients evaluated for ventricular dyssynchrony by echocardiography between February 1999 and May 2007 who subsequently received CRT. Patients were reassessed for signs of reverse remodelling after a mean follow-up of 10 months. Information on vital status was obtained from local registration authorities.
Results  Three parameters significantly predicted reverse remodelling in the logistic regression analysis: the Q-to-E-wave-delay (QED) at a cutoff of 550 ms (odds ratio 4·5, P -value 0·001), the interventricular mechanical delay (IVMD) at a cutoff of 60 ms (odds ratio 2·4, P -value 0·02), and the aortic electromechanical delay (A-EMD) at a cutoff of 140 ms (odds ratio 2·9, P -value 0·004). Furthermore, the QED and the IVMD also predicted all-cause mortality (hazard ratio 0·36, P -value 0·02 and 0·21, P -value 0·004, respectively). Adjustment for confounders did not alter the results.
Conclusions  The QED and IVMD predict reverse remodelling and survival following CRT. These parameters are easy to obtain, provide valuable prognostic information, and should thus be measured in CRT candidates evaluated by echocardiography.     

Fetal nuchal oedema: associated malformations and chromosomal defects.

During an 8-year period, oedema in the dorsal cervical region that produces a characteristic tremor on ballotement of the fetal head (nuchal oedema) was observed in 145 (7%) of the 2,086 fetuses that underwent karyotyping in our unit because of fetal malformations and/or growth retardation. Nuchal oedema was distinguished from nuchal cystic hygromata and from hydrops foetalis. In 132 (91%) of the cases with nuchal oedema, there were other fetal malformations, and 53 (37%) fetuses had chromosomal abnormalities, mainly trisomy 21 but also other trisomies, deletions or translocations, triploidy and Turner syndrome. Furthermore, the chromosomally normal fetuses with nuchal oedema had a very poor prognosis because, in many cases, there was an underlying skeletal dysplasia, a genetic syndrome or cardiac defect.     

Corneal flap displacement and drift in LASIK: comparison of Hansatome and Automated Corneal Shaper microkeratomes

PURPOSE: To describe and compare the displacement of corneal flaps created during laser in situ keratomileusis (LASIK) procedures performed with two different microkeratomes and analyze parameters (for example, pupil-to-hinge distance, drift during suction) that might affect the flap displacement or be influenced by flap displacement. DESIGN: This work was based on a cross-sectional study design. METHODS: Images copied from video recordings of 206 consecutive LASIK surgeries were analyzed to determine the distance from pupil center to corneal flap hinge (pupil-to-hinge distance), the hinge size, the distance from the center of the pupil to the margins of the flap, and the positions of the suction ring before and after vacuum in corneal flaps created by the Hansatome and the Automated Corneal Shaper (ACS) microkeratomes. Accurate measurements of all these variables could be obtained in 121 eyes (Hansatome: n = 66, right eye (OD) = 27 eyes, left eye (OS) = 39 eyes; ACS: n = 55, OD = 25 eyes, OS = 30 eyes), which were included in the analysis. Formulas were derived to calculate from the measurements the magnitude and direction of the drift of the suction ring during vacuum and the final displacement of the corneal flap. RESULTS: The mean +/- standard deviation (SD) drift of eyes during suction with the Hansatome was 0.27 +/- 0.02 mm and with the ACS was 0.12 +/- 0.02 mm (P <.001). The Hansatome induced, on average, more biased (temporal vs random) drift than did the ACS. The mean final displacement of the center of the flap from the center of the pupil was of equal magnitude for the two instruments (0.37 +/- 0.02 mm and 0.36 +/- 0.02 mm with the Hansatome and ACS, respectively). CONCLUSION: The drift induced by the Hansatome contributes to the horizontal component of the final decentration of the corneal flaps. This tendency for drift and the resultant decrease in pupil-to-hinge distance should be considered to minimize flap displacements during LASIK.     

Human corneal epithelial cell viability and morphology after dilute alcohol exposure

PURPOSE: To determine the effect of dilute alcohol on human corneal epithelial cellular morphology and viability. Dilute alcohol is used for epithelial removal during photorefractive keratectomy (PRK) and laser subepithelial keratomileusis (LASEK). METHODS: Corneal epithelial sheets harvested from human eyes after alcohol application during PRK were examined by light and electron microscopy (specimens I-IV). In addition, tissue cultures of human epithelial sheets were monitored for epithelial migration and attachment (specimens V-VII). To determine the effect of dilute alcohol on epithelial cell viability, simian virus (SV)40-immortalized human corneal epithelial cells were exposed to dilute alcohol in distilled water (EtOH-H2O) or to keratinocyte serum-free medium (EtOH-KSFM) for incubation periods of 20 to 45 seconds and concentrations of 10% to 70%. Cell membrane permeability and intracellular esterase activity were analyzed by calcein-acetoxymethyl ester (AM)/ethidium homodimer assay. TdT-mediated dUTP nick-end labeling (TUNEL) assay was used to detect apoptotic cells at 0, 8,12, 24, and 72 hours. RESULTS: Electron microscopy showed varying degrees of basement membrane alterations after alcohol application, including disruptions, discontinuities, irregularities, and duplication (specimens I-IV). Cellular destruction and vacuolization of basal epithelial cells associated with absent basement membrane were also observed (specimen III). One of three cultured epithelial sheets showed attachment and outgrowth in the tissue culture until day 15 (specimen V). Twenty-second exposure of cultured immortalized human cells to various concentrations of EtOH-H2O showed significant reduction of viable cells when EtOH-H2O concentration exceeded 25% (P = 0.005). Increasing the duration of application of 20% EtOH-H2O beyond 30 seconds resulted in a significant reduction in viable cells (69.69% +/- 16.34% at 30 seconds compared with 2.14% +/- 2.29%, 10.45% +/- 7.11%, and 11.09% +/- 15.73% at 35, 40, and 45 seconds, respectively; P = 0.01). TUNEL assay of cultured human corneal epithelial cells exposed to 20% EtOH-H(2)O for 20 and 40 seconds showed maximal labeling at 24 hours (58.05% +/- 33.10%) and 8 hours (94.12% +/- 1.21%), respectively. Exposure to 20% EtOH-KSFM for 20 and 40 seconds resulted in substantially lower TUNEL positivity (3.51% +/- 0.20% at 24 hours and 7.11% +/- 0.49% at 8 hours). CONCLUSIONS: The viability and electron microscopic findings in the basement membrane zone showed significant variation after treatment of the epithelium in vivo with dilute alcohol. The application of dilute alcohol on the monolayer of cultured corneal epithelial cells resulted in increasing cell death in a dose- and time-dependent manner.