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1.
Int Ophthalmol ; 43(8): 2669-2677, 2023 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-36894822

RESUMO

PURPOSE: To assess and compare the efficiency of quick response (QR) code versus telephone contact for post-discharge follow-up in patients receiving low-risk ophthalmic day surgery. METHODS: One hundred and sixty patients undergoing strabismus day-care surgery with general anesthesia were randomly allocated to either the intervention group using QR code (QR group) or the control group receiving telephone call (TEL group) for post-discharge follow-up. The primary outcome was the follow-up overall attendance rate on the second postoperative day. Secondary outcomes included attendance rate at the first scheduled follow-up, number of text message reminders, elapsed time and estimated cost for follow-up, omission rate of follow-up responses, and patient satisfaction. RESULTS: The overall attendance rate of follow-up was significantly higher in the QR group than that in the TEL group (97.5% vs. 87.5%, p = 0.016). As compared with the TEL group, the QR group significantly reduced the number of text message reminders with higher attendances at the first scheduled follow-up (p < 0.001, p = 0.001). Besides, the TEL group cost a median time of 258 s and a median cost of RMB 5.8 yuan to complete a follow-up consultant, but was associated with a significantly high omission rate of follow-up responses comparing to the QR group (p = 0.002). Patient satisfaction was comparable between two groups. CONCLUSION: QR code follow-up can be more efficient than traditional telephone contact in assessing the post-discharge recovery after strabismus day surgery, which provides a safe and intuitively alternative follow-up pathway for identifying issues that may necessitate further clinical care for more low-risk ophthalmic day surgeries.


Assuntos
Assistência ao Convalescente , Alta do Paciente , Humanos , Seguimentos , Procedimentos Cirúrgicos Ambulatórios , Telefone
2.
J Perianesth Nurs ; 35(6): 586-591.e1, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-32855052

RESUMO

PURPOSE: To verify the feasibility of the clinical-based discharge (CBD) criteria and identify the reasons of long postanesthesia care unit length of stay (PACU-LOS) for ophthalmic ambulatory surgical patients under general anesthesia. DESIGN: A prospectively observational study conducted at a tertiary eye center in China. METHODS: Medical records were collected from patients admitted for strabismus ambulatory surgery under general anesthesia from September 2018 to March 2019. The patients were discharged home once met the CBD criteria based on a combination of the modified Aldrete's scoring system and Chung's Post-Anesthetic Discharge Scoring System. Postoperative complications were recorded in the PACU and within 24 hours after discharge. Multivariate logistic regression was applied to identify the factors relating to late discharges. FINDINGS: All patients (N = 400) were safely and successfully same-day discharged home as none of the patients informed severe emergency events or unanticipated readmission. Nine displayed discharge delays mainly because of mild postoperative nausea and vomiting (PONV) although met the discharge criteria. About 85.5% of patients were discharged within a PACU-LOS of 150 minutes, 379 (94.8%) were within 180 minutes, and the cutoff time in PACU-LOS was 150 minutes. Multivariable analysis indicated that sevoflurane anesthesia and the presence of PONV were related to late discharges (PACU-LOS of greater than 150 minutes, all P < .05). CONCLUSIONS: The CBD criteria can efficiently and safely guide the ophthalmic ambulatory surgical patients to discharge home on the same-surgery day, whereas sevoflurane anesthesia and the presence of PONV are associated with a relatively long PACU-LOS.


Assuntos
Procedimentos Cirúrgicos Ambulatórios , Alta do Paciente , Procedimentos Cirúrgicos Ambulatórios/enfermagem , Período de Recuperação da Anestesia , Anestesia Geral/efeitos adversos , China , Humanos , Tempo de Internação
3.
Am J Emerg Med ; 35(8): 1126-1130, 2017 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-28347608

RESUMO

OBJECTIVES: Mucosal atomization device (MAD) was designed to increase the bioavailability of intranasal medications by facilitating absorption, the present study aimed to evaluate and compare the sedation effects of intranasal dexmedetomidine delivered as drops versus sprays on pediatric responses to intravenous cannulation. METHODS: One hundred and six pediatric patients (aged from 2 to 5years) scheduled for elective ophthalmic surgery were intranasally received a dose of 2µg/kg in 20µl/kg of dexmedetomidine for sedation to reduce response to venous cannulation. The patients were randomized into syringe group and MAD group in which dexmedetomidine was delivered as drops or sprays via syringe or MAD respectively. The primary outcome was the response to peripheral vein cannulation assessed by the FLACC scores (faces, legs, activity, cry and consolability) 30min after intranasal administration of dexmedetomidine. The secondary outcomes included acceptance for intranasal medication, sedation onset time, and needle insertion times and any adverse event at the preoperative holding area. RESULTS: The FLACC scores in MAD group were significantly decreased than that treated by drops (P=0.021). The acceptance for intranasal administration between both groups was comparable (P>0.05), the onset time and the incidences in two and more times of needle insertion did not differ significantly between syringe and MAD groups (all P>0.05). None of patients were required to clinically intervene in heart rates reduction and none suffered respiratory depression after administrations of dexmedetomidine in either group. CONCLUSION: Intranasal dexmedetomidine by sprays offers better sedation effects to reduce responses to venous cannulation than drops.


Assuntos
Cateterismo Periférico/métodos , Sedação Consciente/métodos , Dexmedetomidina/administração & dosagem , Hipnóticos e Sedativos/administração & dosagem , Nebulizadores e Vaporizadores , Soluções Oftálmicas/administração & dosagem , Procedimentos Cirúrgicos Oftalmológicos , Administração Intranasal , Cateterismo Periférico/efeitos adversos , Pré-Escolar , China , Protocolos Clínicos , Esquema de Medicação , Feminino , Frequência Cardíaca/efeitos dos fármacos , Humanos , Masculino , Procedimentos Cirúrgicos Oftalmológicos/métodos , Resultado do Tratamento
4.
Paediatr Anaesth ; 27(6): 629-636, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28414899

RESUMO

BACKGROUND AND AIM: Pediatric ophthalmic examinations can be conducted under sedation either by chloral hydrate or by dexmedetomidine. The objective was to compare the success rates and quality of ophthalmic examination of children sedated by intranasal dexmedetomidine vs oral chloral hydrate. METHODS: One hundred and forty-one children aged from 3 to 36 months (5-15 kg) scheduled to ophthalmic examinations were randomly sedated by either intranasal dexmedetomidine (2 µg·kg-1 , n = 71) or oral chloral hydrate (80 mg·kg-1 , n = 70). The primary endpoint was successful sedation to complete the examinations including slit-lamp photography, tonometry, anterior segment analysis, and refractive error inspection. The secondary endpoints included quality of eye position, intraocular pressure, onset time, duration of examination, recovery time, discharge time, any side effects during examination, and within 48 h after discharge. RESULTS: Sixty-one children were sedated by dexmedetomidine with a success rate of 85.9%, which is significantly higher than that by chloral hydrate (64.3%) [OR 3.39, 95% CI: 1.48-7.76, P = 0.003]. Furthermore, children in the dexmedetomidine group displayed better eye position in anterior segment analysis than in chloral hydrate group median difference. All children displayed stable hemodynamics and none suffered hypoxemia in both groups. Oral chloral hydrate induced higher percentages of vomiting and altered bowel habit after discharge than dexmedetomidine. CONCLUSIONS: Intranasal dexmedetomidine provides more successful sedation and better quality of ophthalmic examinations than oral chloral hydrate for small children.


Assuntos
Hidrato de Cloral , Sedação Consciente/métodos , Dexmedetomidina , Olho , Hipnóticos e Sedativos , Exame Físico/métodos , Administração Intranasal , Administração Oral , Catarata/congênito , Catarata/diagnóstico , Pré-Escolar , Hidrato de Cloral/administração & dosagem , Hidrato de Cloral/efeitos adversos , Sedação Consciente/efeitos adversos , Dexmedetomidina/administração & dosagem , Dexmedetomidina/efeitos adversos , Feminino , Humanos , Hipnóticos e Sedativos/administração & dosagem , Hipnóticos e Sedativos/efeitos adversos , Lactente , Masculino , Resultado do Tratamento
6.
Ying Yong Sheng Tai Xue Bao ; 13(10): 1231-4, 2002 Oct.
Artigo em Zh | MEDLINE | ID: mdl-12557665

RESUMO

The growth and competition of a C3 crop rice and a C4 weed, barnyardgrass under FACE(free-air carbon dioxide enrichment) conditions were studied by field experiment. The results showed that under FACE condition, the biomass and yield, leaf number, tiller number, and leaf area index of rice increased, while those of barnyardgrass decreased. Both of the leaf area indexed of rice and barnyardgrass were decreased, while their net assimilation rate increased. When the ratio of planting density of rice and barnyardgrass was 1:1, all of the ratio of biomass, yield, leaf area index, tiller and net assimilation rate were increased under FACE condition. It indicated that the competition between rice and barnyardgrass changed under FACE condition. The competition ability of rice(C3 crop) was enhanced relatively, while that of barnyardgrass weakened.


Assuntos
Dióxido de Carbono/fisiologia , Echinochloa/fisiologia , Oryza/fisiologia , Ecossistema , Folhas de Planta/fisiologia
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