Changes in Vital Signs and Pupil Diameter Related to Pharmacologic Mydriasis in Premature Infants: A Randomized Double Blind Clinical Study

Retinopathy of Prematurity Clinical Trial

Official title: Changes in Vital Signs and Pupil Diameter Related to Pharmacologic Mydriasis in Premature Infants: A Randomized Double Blind Clinical Study

Status Completed

Clinical Trial Summary

Retinopathy of prematurity (ROP) is one of the common anatomic causes of blindness among Filipinos, accounting for 47.7% of the cases. With this retinopathy being preventable and treatable, ROP screening has been proven to be effective in preventing blindness, which is achieved with the usage of mydriatics. Even if the regimen of multiple alternate instillations of 0.5% tropicamide and 2.5% phenylephrine is the one recommended by international guidelines for ROP screening, the mydriatic regimen used by many of the country's institutions is the single instillation of 0.5% tropicamide + 0.5% phenylephrine applied via a cotton wick placed in the inferior fornix (SIW). There have been no studies yet on the safety and efficacy in premature infants of this mydriatic preparation and method, although it is hypothesized that the usage of a cotton wick promotes the possible systemic effects of the mydriatic combination used. This study then aims to determine the safety and efficacy of different mydriatic regimens in premature infants referred for screening of ROP using (1) multiple alternate instillations of 0.5% cyclopentolate hydrochloride and 2.5% phenylephrine (MAI), (2) single instillation of 0.5% tropicamide + 0.5% phenylephrine (SI), and (3) single instillation of 0.5% tropicamide + 0.5% phenylephrine with a cotton wick placed in the inferior fornix (SIW) in a tertiary Philippine hospital. This study was designed as a randomized, double blind, clinical study which enrolled sixty preterm infants referred for ROP Screening from January to July 2011. With instillations via MAI, SI, and SIW, systolic blood pressure (SBP), diastolic pressure (DBP), mean arterial pressure (MAP), heart rate, and oxygen saturation were monitored from ten minutes prior to instillation up to forty-five minutes after instillation. Pupil dilations were also measured at the forty-fifth minute.

Clinical Trial Description

I. Introduction Retinopathy of prematurity (ROP) is one of the common anatomic causes of blindness among Filipinos, accounting for 47.7% of the cases. With this retinopathy being preventable and treatable, ROP screening has been proven to be effective in preventing blindness, which is achieved with the usage of mydriatics. Even if the regimen of multiple alternate instillations of 0.5% tropicamide and 2.5% phenylephrine is the one recommended by international guidelines for ROP screening, the mydriatic regimen usually used by many of the country's institutions is the regimen of 0.5% tropicamide + 0.5% phenylephrine applied via a cotton wick placed in the inferior fornix. There have been no studies yet on the safety and efficacy in premature infants of this mydriatic preparation and method, although it is hypothesized that the usage of a cotton wick promotes the possible systemic effects of the mydriatic combination used. II. Significance It is the aim of this study to evaluate the safety and efficacy of the mydriatic regimens we use in our institution and compare it to the recommendation by the UK ROP Guidelines. In doing so, this study aims to (1) document vital sign changes in the infant during dilation, (2) identify adverse systemic changes due to the mydriatic regimen and (3) provide appropriate interventions and recommendations to address these adverse effects. These will greatly improve the ROP screening process in our institution. III. Objectives The general objective is to determine vital sign changes related to Pupil Dilation among preterm infants referred for ROP Screening from Neonatal Intensive Care Unit, Pediatric Wards and Eye Instrumentation Center of the Philippine General Hospital (PGH). Specifically, its objective is to compare the vital sign changes and mydriasis in (1) multiple alternate instillations of 0.5% Cyclopentolate Hydrochloride + 2.5% Phenylephrine (MAI) (2) single instillation of 0.5%/0.5% Phenylephrine + Tropicamide (SI) and (3) single instillation of 0.5%/0.5% Phenylephrine + Tropicamide with a cotton wick placed in the inferior fornix (SIW). IV. Methodology This study was designed as a randomized, double blind, clinical study which enrolled sixty preterm infants referred for ROP Screening from January to July 2011. Each subject was randomly distributed into the standard, instillation, and packing group. To avoid observer bias, two investigators were involved per monitoring during dilation. The first investigator was assigned only to place the monitoring devices and to administer the mydriatics contained in unmarked 1 mL syringe which content was unknown to him. The vital signs monitored during dilation were blood pressures (systolic, diastolic and mean arterial pressure (MAP)), heart rates and oxygen saturations using the newly calibrated Phillips Digital IntelliVue MP20 junior Cardiac monitors. A digital camera and a millimeter rule were used to approximate size of pupil dilatation. Measurement of all the vital signs and pupil dilation from a subject was derived from a single dilation session only. Prior to data collection up to the end of monitoring, other factors that may affect the vital signs of the preterm infants were addressed. This included hunger, cold temperature, and soiled diapers. Baseline vital signs determination was then performed 10 and 5 minutes prior to the first drop of mydriatic or proparacaine prior to packing. Additional reading will be done if there is a significant difference in the vital signs between 10 and 5 minutes prior to the initial drop. For the MAI, multiple alternate drops of 0.5% cyclopentolate then 2.5% phenylephrine every 5 minutes in two doses were instilled (total of 0.2 milliliter of 0.5% cyclopentolate and 0.2 millimeter of 2.5% Phenylephrine). Vital signs were continuously recorded at time 0, 5, 10, 15, 20, 25, 30, 35, 40 and 45. At the 45th minute, a lid retractor was placed in the eyes of the subject after a drop of topical anesthesia. Pictures of the eyes were taken with a millimeter rule to serve as measurement reference. For the SI, only a drop of 0.5%/0.5% tropicamide + phenylephrine was properly instilled at time 0 (total of 0.1 milliliter). Vital signs were continuously recorded at time 0, 5, 10, 15, 20, 25, 30, 35, 40 and 45. At the 45th minute, a lid retractor was placed in the eyes of the subject after a drop of topical anesthesia. Pictures of the eyes were taken with a millimeter rule to serve as measurement reference. For the SIW, a cotton wisp soaked with a drop of 0.5%/0.5% tropicamide + phenylephrine was placed on the lower fornix in each eye of the infant (total of 0.1 milliliter). The weight of the cotton wisp was standardized at 0.02 milligram using a digital weighing scale. Vital signs were continuously recorded at time 0, 5, 10, 15, 20, 25, 30, 35, 40 and 45. At the 45th minute, a lid retractor is placed in the eyes of the subject after a drop of topical anesthesia. Pictures of the eyes were taken with a millimeter rule to serve as measurement reference. Pictures were uploaded into the computer monitor for the actual measurement. Vital sign changes were monitored using the newly calibrated Phillips Digital IntelliVue MP20 junior Cardiac monitors. In the presence of significant vital sign changes, immediate intervention will be done. In the presence of a significant increase in BP or heart rate, the infant will be observed. Both changes are expected from undergoing a stressful procedure such as placing a lid retractor in measuring the pupil dilation. The infant will be referred to the NICU ROD for further work up should tachycardia persist even after the examination. The blood pressure, heart rate and sensorium will be continuously monitored so as to avoid any ensuing bradycardia. In the presence of a significant drop in BP, the infant will be referred to the NICU ROD for further work up to determine the possible source. Fluid challenge will be done to check if the cause of hypotension is just attributable to hypovolemia. The investigator will determine body temperature to check for hypothermia. If hypothermic, slow rewarming will be done by placing back the infant inside a close incubator or beside a radiant warmer. Blood glucose will be checked for hypoglycemia. Should hyperglycemia be detected, the infant can be started on 2cc/kg D5water. Infant will be worked up for infection as well. During events of hypoxia or oxygen desaturation of less than 85%, the infant will be given supportive ventilation as required. Oxygen saturation will be monitored using the pulse oximeter. In the event of an apnea happening, supportive ventilation will be provided immediately, together with significant stimulation. The infant will be referred to the NICU ROD for possible intubation. In the event of bradycardia, significant stimulation will be started on the infant. The infant will be referred to the NICU ROD for further work-up to determine the cause. The investigator is also to determine body temperature to check for hypothermia. If hypothermic, slow rewarming will be done by placing back the infant inside a close incubator or beside a radiant warmer. Blood glucose will be determined to check for hypoglycemia. Should hyperglycemia be detected, the infant can be started on 2cc/kg D5water. Infant can be worked up for infection as well. In the event that a subject suffers from any of the abovementioned adverse effects, the appropriate interventions cited will be administered free of charge. Should the adverse effects believed by the investigators to be secondary to the ROP screening only and additional expenses are needed to procure medicines or equipment, the investigators will shoulder the expenses. If the medicine or equipment is immediately needed, the relative may spend first for them and have the expenses reimbursed with the investigators later. Should the amount to procure the said medicine or equipment cannot be produced by the relative, the investigators can be immediately contacted to assist the relatives immediately. All other expenses will be shouldered by the investigators through reimbursements. Expenses amounting to P500 for the medicine and P1000 for the equipment will be shouldered by the investigators. Should it exceed these limits, the infant will be referred to any charitable institution for further assistance. The blood pressure (systole, diastole and MAP), HR and oxygen saturation obtained during dilatation were analyzed. They were graphed to determine patterns from baseline up to 45 minutes. Wilcoxon signed rank test was used to assess statistical significance for oxygen saturation, being a non-parametric variable. Poor dilatation among ROP patients with the advanced disease will be noted. A subgroup analysis was also done to determine the any relationship between the amounts of mydriatic used to the weight of the infant. An interim analysis was done within the study to assess if the two mydriatic regimens were particularly beneficial or harmful compared to the concurrent standard group. Either the Pocock or the Flemming method will be used to decide if this study needed to terminate earlier than planned. Unblinding can be done should it be made necessary during the interim analysis or during course of the study. This protocol was submitted to the PGH ERB for ethics review and approval. It was conducted only upon approval from the ERB. All patient information were anonymized and are confidential. There is no funding received by the investigators for the conduct of this research. ;

Related Conditions & MeSH terms

• Mydriasis
• Retinopathy of Prematurity

• NCT number: NCT04838665
• Study type: Interventional
• Source: University of the Philippines
• Status: Completed
• Phase: Phase 4
• Start date: September 30, 2011
• Completion date: September 30, 2011