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Pattern and Prevalence of Color Vision Disorders amongst Secondary School Students in Rivers State, Nigeria
Study Design: A community based descriptive cross sectional study.
Place and Duration of Study: Department of Ophthalmology, University of Port Harcourt Teaching Hospital from the 20th of January to the 30th of April 2014.
Methodology: A community based descriptive cross sectional study where study subjects were selected using multi-stage random sampling technique with inclusion criteria of consenting students with visual acuity >6/24. Ethical clearance for test was obtained from institution. Socio-demographic data obtained using an interviewer administered questionnaire. A comprehensive ocular examination was done and color vision assessed using the Ishihara 24 plate 2009 edition and the Farnsworth Munsell D 15 test for those who failed the Ishihara test. The prevalence of color vision disorder was determined by those that failed the Ishihara test.
Data obtained was analyzed using SPSS version 21. Mean and standard deviations were determined for age. The age groups gender, other demographic distribution of the subjects amongst other was presented using frequency tables and charts.
Statistical significance was put at p ≤ 0.05.
Results: 1000 students were studied which consisted of four hundred and ninety five males (n=495; 49.4%) and five hundred and six females (n=506; 50.6%), with a male female ratio of 1:1.02. Mean age of subjects was 14.3±1.8 years with an age range of 9-20 years. The prevalence of color vision disorders was 2.8% (p-value 0.000) and was higher in males (2.1%) than females (0.7%) (P-value 0.000). Deutan defects were the most predominant (1.8%) compared to protan defects (0.4%) and tritan defects (0.2%).
Conclusion: The study showed a prevalence of color vision disorders of 2.8% with male preponderance among secondary school students. Deutan color vision defects were most prevalent.
Please read full article : - www.journalor.com
Comparitive Study of Bupivacaine with Nalbuphine and Bupivacaine alone for Post-Operative Analgesia in Subarachnoid Block for Lower Limb Surgeries- Prospective Randomised Study-Juniper Publishers
Background: Nalbuphine is a synthetic opioid , with kappa agonist or partial µ antagonist action. When added as an adjuvant to intrathecal bupivacaine, it acts on dorsal horn of spinal cord producing analgesia with decreased incidence of µ receptor side effects.
Aims and Objectives: To compare the onset, duration of sensory blockade, duration of motor blockade, 2 segment regression and duration of post operative analgesia achieved, by comparing hyperbaric bupivacaine alone with hyperbaric bupivacaine and nalbuphine after intrathecal administration.
Material and Methods: Randomised double blind study done on 60 patients, who were undergoing lower limb surgeries under subarachnoid block. Patients were divided into two groups, group B receiving 15mg of 0.5% hyperbaric bupivacaine+0.1ml of normal saline and group N receiving 15mg of hyperbaric bupivacaine+0.1ml of nalbuphine (1mg). Assessment of duration of motor and sensory blockade was done by modified bromage scale and pin prick method respectively.
Results: There was no significant variation in onset of motor and sensory blockade in two groups, but mean time of post-operative analgesia in group N was highly significant than group B(P<0.001).
Conclusion: Thus we conclude that intrathecalnalbuphine at dosage of 1mg can be used as effective adjuvant along with 0.5% of hyperbaric bupivacaine intrathecally to have good post-operative analgesia.
Keywords: Nalbuphine; Modified bromage scale; Sub-arachnoid block; hyperbaric bupivacaine
Nalbuphine is an opioid, which is structurally related to oxymorphone, highly lipid soluble with an agonist activity at kappa and an antagonist activity at µ opioid receptor .
When nalbuphine is added as an adjuvant to intrathecal bupivacaine, it has potential to provide good intraoperative and post operative analgesia with decreased incidence of µ receptor side effectslike respiratory depression . The side effects of nalbuphine are like dizziness, bradycardia, nausea, vomiting, pruritis, urinary retention and sedation. Nalbuphine has short duration of action due to its lipid solubility and rapid clearance when compared to morphine .
Here we compared the effect of nalbuphine addition to hperbaric bupivacaine intrathecally with hyperbaric bupivacaine alone for duration, quality of post operative analgesia and any side effects.
- Onset of sensory and motor blockade.?
- Duration of sensory and motor blockade.
- 2 segment regression.
- Duration of post operative analgesia achieved
- To study any side-effects with addition of nalbuphine.
- Haemodynamic parameters.
The study was undertaken after obtaining ethical committee clearance as well as informed consent from all patients. The sample size was decided in consultation with the statistician and was based on initial pilot study observations, indicating that approximately 23 patients should be included in each group in order to ensure a power of 0.80. Assuming a 5% drop out rate, the final sample size was set at 30 patients in each group, which would permit a type 1 alpha error =0.05, with a type 2 error of beta=0.2.
Study consists of 60 patients of both genders belonging to ASA I and II aged between 18-65 years, who were undergoing lower limb surgeries under sub arachnoid block. Patients were randomly allocated into 2 groups of 30 patients each, group N and group B by computerized randomization method. Group N received 3ml of 0.5% Bupivacaine(15mg)+1mg of Nalbuphine, group B received 3ml of 0.5% of Bupivacaine (15 mg)+0.1ml of normal saline for spinal aneasthesia. Pre anaesthetic check up was done and patients were kept nil per oral for about 6-8 hours. Patient was pre medicated with Tb- Alprazolam 0.5mg and Tb- rantidine 150 mg night before surgery.
- American Society of Anaesthesiologists (ASA) I and II patients.
- Age group of 18-65 years.
- Patient with written valid consent.
- Patient undergoing elective lower limb surgery.
- Infection at the site.
- Bleeding disorder.
- Allergic reaction to any anaesthetic drug.
- Patients on tranquilizers, hypnotics, sedatives and other psychotropic drugs.
Time of spinal anaesthesia (drug administration time)
- Time of onset and complete sensory and motor block
- 2 segment regression of the block.
- Duration of sensory block (sensory level was assessed by pin prick method)
- Duration of post-operative analgesia(effective analgesia-time of onset of sensory block to the first request of analgesia by using VAS score).
- Duration of motor block (which was assessed by modified bromage scale)
1-just able to flex knees, full flexion of feet
2-unable to flex knees, but some flexion of feet possible.
3-unable to move legs/feet
Post operatively pain, sensory level, motor level was evaluated every 30mins for first 2 hours, every 60mins for next 6 hours and at 12 hours and 24 hours in recovery room. Pain was assessed by VAS (visual analogue scale). Here patient was given a scale marked from 0-10 and was asked to mark on the scale the degree of pain he /she experiencing from 0-no pain to 10 maximum pain ,when VAS>3, rescue analgesia given with injdiclofenac sodium.
Side effects like (pruritis, urinary retention, respiratory depression, post operative nausea and vomiting etc) were recorded for 24 hours.
Table 1,2) (Figure 1-3).
Summary of Results
The mean time of onset of sensory blockade and motor blockade between the two groups is comparable with p value of (0.3843) and (p=0.2133) which is not statistically significant. Two segment regression of sensory blockade is significantly prolonged by addition of intrathecalnalbuphine as seen in group N. The duration of analgesia is significantly prolonged with addition of nalbuphine compared with bupivacaine alone.
6]. Most commonly used opioids are usually µ agonist drugs, which has excellent analgesic effect with various µ related side effects. Eventually it was found that significant analgesia can be obtained by action on kappa binding sites also by bypassing p related side effects [7,8]. As there was less studies on opioids like Nalbuphine as an adjuvant in spinal anaesthesia. We have conducted this study
Nalbuphine hydrochloride is a kappa agonist/partial µ antagonist analgesic [8,9]. Whennalbuphine binds to µ receptor,it serves only to competitively displace other µ agonists from the receptor without itself displacing any agonist activity similar to those of nalaxone. It binds to kappa receptor; it has agonist effect, so nalbuphine has mixed agonist-antagonistic effect. These affects inhibit release of neurotransmitter that mediates pain such as substance p and in addition to this it also inhibits post synaptic interneuron and outer neuron of spinothalamic tract which transports nociceptive information.
Local anesthetic bupivacaine acts mainly by blockade of voltage gated sodium channels in the axonal membranes, and also by further effect on presynaptic inhibition of calcium channels . A combination of these affects may explain the observed synergism between bupivacaine and nalbuphine in our study.
The principle finding of this study is that addition of 1mg of intrathecalnalbuphine to spinal anaesthesia in patients undergoing lower limbsurgery with hyperbaric 0.5% bupivacaine intensifies the sensory blockade and increases the duration of sensory blockade without µ related side effects. Two segment regression, time of sensory blockade and duration of analgesia were maximally prolonged with nalbuphine 1mg with minimum effects over haemodynamic and respiratory parameters .
Previous studies have demonstrated that visceral analgesia is mediated by both µ and kappa receptors and that intrathecalnalbuphine suppresses response to visceral pain . In our study 2 segment regression of sensory block was prolonged with addition of nalbuphine to bupivacaine which correlated with that of tiwari et al whoalso found that with addition of 0.8mg of nalbuphine to 0.5% bupivacaine for subarachnoid block provides excellent analgesia with longer duration of action compared with 1.6 and 2.4mg of nalbuphine .
Large number of animal studies has been undertaken to prove that intrathecalnalbuphine was not neurotoxic. Rawal et al showed in sheep model usinghistopathological methods that, intrathecalnalbuphine even at large doses 15-24mg were not associated with histopathological changes of the spinal cord .
From our study we can also conclude that use of nalbuphine in dosage of 1mg along with bupivacaine 0.5% H,does not cause any gross haemodynamic disturbances. Similar findings are seen in study conducted by culebras et al5,tiwari et al , mortafa et al .
In our study none of the patients had respiratory depression since nalbuphine is µ antagonist,respiratory depression is predominantly µ mediated. Respiratory depression effect is expected to be attenuated by nalbuphine, so nalbuphine exhibits ceiling effect for respiratory depression[RR<30cpm,spo2<90%] this is proved in studies done by romagnoli and keats .
Our study also concludes that addition of nalbuphine had significantly longer duration of first request of analgesia, compared to patients who received bupivacaine alone and it also prolongs duration of analgesia which correlates to result of studies done by lin  found that intrathecal nalbuphine at dosage of 0.8-1.6mg improved quality of intraoperative analgesia during cesarean section with good visceral analgesia,our study showed excellent analgesia at dosage of 1mg as an adjuvant to intrathecal bupivacaine . Adverse effects like nausea,vomiting, urinary retention and shivering were statistically insignificant.
Thus we conclude that intrathecalnalbuphine at dosage of 1mg can be used as an effective adjuvant along with intrathecal hyperbaric bupivacaine 0.5% to have a good post operative analgesia.
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