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Background: Chronic myelogenous Leukemia is a form of cancer that was firstly recognizes to associate strongly with the chromosomal abnormality [t (9; 22) translocation] called Philadelphia chromosome. Objective: Philadelphia chromosome is a characteristic chromosomal marker that is associated with chronic myelogenous leukemia. Methods: More than one hundred patients of either sex were selected for the experiment. RNA was isolated from whole blood of patients so can use exclusively in RT-PCR. Results: Philadelphia chromosome in blood samples of patients with suspected diagnosis of CML was detected in 63% of patients. During our experimental studies on CML patients we do not encounter any complex translocation involving chromosome 8, 9 and 22. Conclusions: Philadelphia chromosome is a precise cytogenetic marker the detection of which is significant for differential diagnosis and clinical organization of patients with clinical diagnosis of CML. It is of significant that Ph chromosome occurs in pre-leukemic stage and has great diagnostic significance.
Study Objective: The aim of this study was to evaluate the postoperative morphine-sparing and pain reducing effects of a preemptive, multimodal, perioperative analgesic regimen incorporating the use of preincisional intrathecal blockade plus parenteral anti-inflammatory agents, in patients undergoing lower limb orthopaedic surgery. Study design: Prospective Single blinded Randomized Controlled Trial. Study setting: The Aga Khan Hospital, Nairobi, Kenya. Methods: 44 ASA physical status 1 and 2 patients undergoing lower limb orthopaedic surgery were randomly allocated into two groups of 22 patients each. Patients in the Intervention group were given a preincisional subarachnoid injection of 15mg hyperbaric Bupivacaine and 25mcg Fentanyl, plus, parenteral Paracetamol 20mg/kg and Diclofenac 1mg/kg. Patients in the Control group received a standardized general anaesthetic protocol consisting of Midazolam and Propofol, Oxygen, N2O, Isoflurane and cis-atracurium. Analgesia intraoperatively was maintained by remifentanil 0.1-0.3mcg/kg/min with Paracetamol 20mg/kg and Diclofenac 1mg/kg given at the end of surgery. PCA morphine 2mg/ml was instituted once the patient complained of pain. Intramuscular rescue doses of 10mg morphine were administered on patient request. Visual analog score (VAS) was used to assess pain over 48 hours, the cumulative PCA morphine dose and the total number of morphine rescue doses requested were calculated and compared for both groups. Results: 44 consecutive patients undergoing lower limb orthopaedic surgery completed the study (Intervention group, n=22; Control group n=22). The cumulative PCA morphine consumption at 2, 24 and 48 hours following patient first request for the control and intervention groups were 6.72 ± 6.33mg versus 5.72 ± 7.62mg ( P=0.6383), 19.682 ± 16.50mg versus 24.09 ± 17.83mg (P=0.3995), 34.409 ± 32.99mg versus 34.818 ± 23.11mg (P=0.9622) respectively. The mean difference in the number of Intramuscular 10mg morphine rescue doses requested by the patients between the control and intervention groups at 48 hours was 8.1818 ± 19.673 versus 3.2727 ± 9.228 (P=0.295). The median VAS at 2 hours was significantly lower in the intervention than control group, 5 ± 2.17 versus 3 ± 2.37 (P=0.0068). VAS at 6, 12, 24, 48 and 72 hours postoperatively were not significantly different between the two groups. The McGill pain questionnaire present pain intensity showed a significant difference between the control and intervention group, 2.31 ± 0.70 versus 1.81 ± 0.65 (P=0.00001). There was no significant difference in the pain rating index between the control and intervention group, 8.681 ± 2.46 versus 8.59 ± 2.30 (P= 0.8998). Conclusion: A non-statistically significant trend towards a