Patient satisfaction and follow-up adherence to glaucoma case management clinic in China.

AIM: To assess glaucoma patient satisfaction and follow-up adherence in case management and identify associated predictors to improve healthcare quality and patient outcomes. METHODS: In this cross-sectional study, a total of 119 patients completed a Patient Satisfaction Questionnaire-18 and a sociodemographic questionnaire. Clinical data was obtained from the case management system. Follow-up adherence was defined as completing each follow-up within ±30d of the scheduled time set by ophthalmologists during the study period. RESULTS: Average satisfaction scored 78.65±7, with an average of 4.39±0.58 across the seven dimensions. Age negatively correlated with satisfaction (P=0.008), whilst patients with follow-up duration of 2 or more years reported higher satisfaction (P=0.045). Multivariate logistics regression analysis revealed that longer follow-up durations were associated with lower follow-up adherence (OR=0.97, 95%CI, 0.95-1.00, P=0.044). Additionally, patients with suspected glaucoma (OR=2.72, 95%CI, 1.03-7.20, P=0.044) and those with an annual income over 100 000 Chinese yuan demonstrated higher adherence (OR=5.57, 95%CI, 1.00-30.89, P=0.049). CONCLUSION: The case management model proves effective for glaucoma patients, with positive adherence rates. The implementation of this model can be optimized in the future based on the identified factors and extended to glaucoma patients in more hospitals.

Ag/AgxH3-xPMo12O40 Nanowires with Enhanced Visible-Light-Driven Photocatalytic Performance.

Photocatalysis, a promising technology platform to address the environmental problems, has been attracting considerable attention. In this paper, Ag/AgxH3-xPMo12O40 (simplified as Ag/AgHPMo12) nanowires have been synthesized by a facile solid reaction route and in situ photodeposited method. The results of SEM and TEM indicate that the diameters of AgHPMo12 nanowires are about 45 ± 10 nm, and Ag nanoparticles with diameters in the range of 5-15 nm are uniformly anchored on the surface of AgHPMo12 nanowires. The Ag content in the Ag/AgHPMo12 composite was manipulated by the light irradiation time (Ag/AgHPMo12-x; x stands for the irradiation time; x = 2, 4, 6, 8 h, respectively). With increasing irradiation time, the light absorption of as-synthesized samples in the visible region was gradually enhanced. The Ag/AgHPMo12-4 exhibits the best photocatalytic performance for the degradation of methyl orange and reduction of Cr2O72- under visible-light (λ > 420 nm) irradiation. The study of the photocatalytic mechanism reveals that both Ag and AgHPMo12 can be excited by visible light. The photoinduced electrons were transferred from AgHPMo12 to metallic Ag, and combined with the Ag plasmonic holes. The Ag plasmonic electrons were trapped by O2 to form ·O2-, or directly reduced Cr2O72- to Cr3+. Meanwhile, the ·O2- species and the photogenerated holes of AgHPMo12 were used to oxidize MO or i-PrOH; thus, they showed highly efficient and recyclable photocatalytic performance for removing the organic and inorganic pollutants.

A Surfactant-Encapsulating Polyoxometalate Nanowire Assembly as a New Carrier for Nanoscale Noble-Metal Catalysts.

The loading of noble-metal nanoparticles (NMNPs) onto various carriers to obtain stable and highly efficient catalysts is currently an important strategy in the development of noble metal (NM)-based catalytic reactions and their applications. We herein report a nanowire supramolecular assembly constructed from the surfactant-encapsulating polyoxometalates (SEPs) CTAB-PW12 , which can act as new carriers for NMNPs. In this case, the Ag NPs are loaded onto the SEP nanowire assembly with a narrow size distribution from 5 to 20 nm in diameter; the average size is approximately 10 nm. The Ag NPs on the nanowire assemblies are well stabilized and the over agglomeration of Ag NPs is avoided owing to the existence of well-arranged polyoxometalate (POM) units in the SEP assembly and the hydrophobic surfactant on the surface of the nanowire assembly. Furthermore, the loading amount of the Ag NPs can be adjusted by controlling the concentration of the AgNO3 aqueous solution. The resultant Ag/CTAB-PW12 composite materials exhibit high activity and good stability for the catalytic reduction of 4-nitrophenol (4-NP) with NaBH4 in isopropanol/H2 O solution. The NMNPs-loaded SEP nanoassembly may represent a new composite catalyst system for application in NM-based catalysis.

Keggin-Type Polyoxometalate-Based Metal-Organic Networks for Photocatalytic Dye Degradation.

The reaction of Keggin-type polyoxometalate (POM) units, transition-metal (TM) ions, and a rigid bis(imidazole) ligand (1,4-bis(1-imidazolyl)benzene (bimb)) in a hydrothermal environment led to the isolation of four new POM-based metal-organic networks, [H2 L][CuL][SiW12 O40 ]⋅2 H2 O (1), [H2 L]2 [Co(H2 O)3 L][SiW11 CoO39 ]⋅6 H2 O (2), KH[CuL]2 [SiW11 CoO39 (H2 O)]⋅2 H2 O (3), and [CuL]4 [GeW12 O40 ]⋅H2 O (4; L=bimb). All four compounds were characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis, powder X-ray diffraction, and single-crystal X-ray diffraction. Compounds 1 and 3 are new 3D networks with 1D channels. Compounds 2 and 4 contain 2D networks, which further stack into 3D supramolecular networks. The contributions of pH value, the negative charge of the POM, and the TM coordination modes to the construction of 3D networks were elucidated by comparing the synthetic conditions and structures of compounds 1-4. The photocatalytic properties of compounds 1-4 were investigated using methylene blue (MB) degradation under UV light. All compounds showed good catalytic activity and structural stability. The possible catalytic mechanism was discussed on the basis of active-species trapping experiments. The different photocatalytic activities of compounds 1-4 were explained by comparison of the band gaps of different POM species and different packing modes of POM units in these hybrid compounds.

Polyoxometalate-based entangled coordination networks induced by an extended bis(triazole) ligand.

The introduction of an extended bridging bis(triazole) ligand, that is, 4,4'-bis(1,2,4-triazol-1-ylmethyl)biphenyl (BBPTZ), into the hydrothermal reaction system containing transition metal ions and Keggin-type polyoxometalates (POMs) led to the isolation of three new organic-inorganic hybrid entangled coordination networks, [Cu(I)2Cu(II)(BBPTZ)6][SiW12O40]⋅12H2O (1), [Ni(BBPTZ)2(H2O)][H2SiW12O40]⋅11H2O (2), and [Ni2(BBPTZ)4(H2O)2][SiW12O40]⋅3H2O (3). All three compounds were characterized by elemental analysis, IR spectroscopy, TG analysis, powder X-ray diffraction, and single-crystal X-ray diffraction. Compound 1 contains a 2-D POM-based metal-organic layer entangled with 1-D ladder-like metal-organic chains. The adjacent 2-D networks are parallel to each other, further stacking into a 3-D supramolecular framework with 1-D channels. Compound 2 exhibits a 1-D cantilever-type loop-containing chain. The Keggin-type POMs act as the cantilever groups, leading to the adjacent catilever-type chains interwaving together to form a 3-D supramolecular open framework with two types of channels. Compound 3 possesses a 3-D open framework based on 2-D metal-organic undulated layer and Keggin-type POM clusters. Three sets of such frameworks further interpenetrate with each other to form an interesting three-fold interpenetrating framework. The photocatalytic activities of compounds 1-3 for the decomposition of methylene blue (MB) under UV light have been investigated.