Athma Prasanna - Academia.edu (original) (raw)
Papers by Athma Prasanna
Journal of Obstetric Anaesthesia and Critical Care, 2011
Regional Anesthesia & Pain Medicine, 1992
Indian Journal of Anaesthesia, 2002
Journal of Obstetric Anaesthesia and Critical Care, 2011
Journal of Pain and Symptom Management, 1996
Gmerpatn, oral mmphine su&te, dim block The use of bilateral neumiytic celiac plexus blolk to rel... more Gmerpatn, oral mmphine su&te, dim block The use of bilateral neumiytic celiac plexus blolk to relieve intractable pain due to tipper abdominal malignancy is' well established.'.A This block is typically performed using a large volume and high concentration of alcoh,bl. Efficacy rates have been in the range oi @I%-94% (good to excellent relief), with varied durations.'S-S" The technique requirss skill and is not free from 'side effects. Wilh the advent of oral opioid therapy, the indications have become more limited. Unilateral neurolytic block ma); have benefit 'in reducing the complications of neurolysis."~' It may also be analgesic and reduce the requirement for oiioids in 'some settings. We describe our experience wi+ this block as an
Journal of Pain and Symptom Management, 1997
The effectiveness of the sphenopalatine ganglion (SPG) block for the relief of symptoms in chroni... more The effectiveness of the sphenopalatine ganglion (SPG) block for the relief of symptoms in chronic vasomotor rhinitis was assessed in 30 patients of both genders. The number of blocks required for complete relief was three (range from two to four) at weekly intervals in 66. 7% of volunteers. There was no recurrence of symptoms during a follow-up period of 12-20 months in 29 patients, and one patient was symptom free for 8 months. The technique is simple and can be performed as an outpatient procedure without side effects.
Middle East journal of anaesthesiology, 2003
Results: Fifty two percent (primi) and 64% (multi) gravida in Group I and 8% in the Group II expe... more Results: Fifty two percent (primi) and 64% (multi) gravida in Group I and 8% in the Group II experienced good to excellent relief of back pain. Eight percent in primi and 12% in multigravida had no relief in Group I. Few had benefit in the second stage. The duration of labor was reduced by 120 minutes in multi and by 77 minutes in primigravida in group I (P value <0.001). There was no change in the intrapartum fetal heart rate in both the groups and none required immediate resuscitation.
Middle East journal of anaesthesiology, 2004
Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdomin... more Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdominal surgery were grouped into sixteen each, on complaint of pain. They received an epidural bolus dose, followed by infusion of the assigned drug at 4ml per hour through BARD PCA I pump. Pain assessment, for the first four hours, was hourly, and subsequently at l0th, 16th, 22nd, 28th, 36th and 40th hour by VAS and VRS. The groups matched for demographic distribution. All groups had lower mean pain scores at first hour by VAS and VRS. In Group II and Group III, the difference was significant (<0.05) at the 2nd (VAS) and 4th (VRS) hours. From 16th (VAS) and 22nd (VRS) hours, the mean pain score was less and significant (<0.05) in Group III. In all groups sedation ranged from 0-1. There was hypotension in Group I (2/16).urinary retention in Group II (8/9 not catheterised); unilateral sensory impairment and motor weakness in Group I (3/16) and Group III (1/16). This study showed that co...
Results: Fifty two percent (primi) and 64% (multi) gravida in Group I and 8% in the Group II expe... more Results: Fifty two percent (primi) and 64% (multi) gravida in Group I and 8% in the Group II experienced good to excellent relief of back pain. Eight percent in primi and 12% in multigravida had no relief in Group I. Few had benefit in the second stage. The duration of labor was reduced by 120 minutes in multi and by 77 minutes in primigravida in group I (P value <0.001). There was no change in the intrapartum fetal heart rate in both the groups and none required immediate resuscitation.
Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdomin... more Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdominal surgery were grouped into sixteen each, on complaint of pain. They received an epidural bolus dose, followed by infusion of the assigned drug at 4ml per hour through BARD PCA I pump. Pain assessment, for the first four hours, was hourly, and subsequently at l0th, 16th, 22nd, 28th, 36th and 40th hour by VAS and VRS. The groups matched for demographic distribution. All groups had lower mean pain scores at first hour by VAS and VRS. In Group II and Group III, the difference was significant (<0.05) at the 2nd (VAS) and 4th (VRS) hours. From 16th (VAS) and 22nd (VRS) hours, the mean pain score was less and significant (<0.05) in Group III. In all groups sedation ranged from 0-1. There was hypotension in Group I (2/16).urinary retention in Group II (8/9 not catheterised); unilateral sensory impairment and motor weakness in Group I (3/16) and Group III (1/16). This study showed that co...
Principles of Anesthesia Equipment, 2016
Middle East journal of anaesthesiology, 2003
Middle East journal of anaesthesiology, 2004
Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdomin... more Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdominal surgery were grouped into sixteen each, on complaint of pain. They received an epidural bolus dose, followed by infusion of the assigned drug at 4ml per hour through BARD PCA I pump. Pain assessment, for the first four hours, was hourly, and subsequently at l0th, 16th, 22nd, 28th, 36th and 40th hour by VAS and VRS. The groups matched for demographic distribution. All groups had lower mean pain scores at first hour by VAS and VRS. In Group II and Group III, the difference was significant (<0.05) at the 2nd (VAS) and 4th (VRS) hours. From 16th (VAS) and 22nd (VRS) hours, the mean pain score was less and significant (<0.05) in Group III. In all groups sedation ranged from 0-1. There was hypotension in Group I (2/16).urinary retention in Group II (8/9 not catheterised); unilateral sensory impairment and motor weakness in Group I (3/16) and Group III (1/16). This study showed that co...
Journal of Pain and Symptom Management, 1997
Journal of Pain and Symptom Management, 1993
Journal of Pain and Symptom Management, 1994
Journal of Pain and Symptom Management, 1993
The Clinical Journal of Pain, 1993
Journal of Obstetric Anaesthesia and Critical Care, 2011
Regional Anesthesia & Pain Medicine, 1992
Indian Journal of Anaesthesia, 2002
Journal of Obstetric Anaesthesia and Critical Care, 2011
Journal of Pain and Symptom Management, 1996
Gmerpatn, oral mmphine su&te, dim block The use of bilateral neumiytic celiac plexus blolk to rel... more Gmerpatn, oral mmphine su&te, dim block The use of bilateral neumiytic celiac plexus blolk to relieve intractable pain due to tipper abdominal malignancy is' well established.'.A This block is typically performed using a large volume and high concentration of alcoh,bl. Efficacy rates have been in the range oi @I%-94% (good to excellent relief), with varied durations.'S-S" The technique requirss skill and is not free from 'side effects. Wilh the advent of oral opioid therapy, the indications have become more limited. Unilateral neurolytic block ma); have benefit 'in reducing the complications of neurolysis."~' It may also be analgesic and reduce the requirement for oiioids in 'some settings. We describe our experience wi+ this block as an
Journal of Pain and Symptom Management, 1997
The effectiveness of the sphenopalatine ganglion (SPG) block for the relief of symptoms in chroni... more The effectiveness of the sphenopalatine ganglion (SPG) block for the relief of symptoms in chronic vasomotor rhinitis was assessed in 30 patients of both genders. The number of blocks required for complete relief was three (range from two to four) at weekly intervals in 66. 7% of volunteers. There was no recurrence of symptoms during a follow-up period of 12-20 months in 29 patients, and one patient was symptom free for 8 months. The technique is simple and can be performed as an outpatient procedure without side effects.
Middle East journal of anaesthesiology, 2003
Results: Fifty two percent (primi) and 64% (multi) gravida in Group I and 8% in the Group II expe... more Results: Fifty two percent (primi) and 64% (multi) gravida in Group I and 8% in the Group II experienced good to excellent relief of back pain. Eight percent in primi and 12% in multigravida had no relief in Group I. Few had benefit in the second stage. The duration of labor was reduced by 120 minutes in multi and by 77 minutes in primigravida in group I (P value <0.001). There was no change in the intrapartum fetal heart rate in both the groups and none required immediate resuscitation.
Middle East journal of anaesthesiology, 2004
Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdomin... more Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdominal surgery were grouped into sixteen each, on complaint of pain. They received an epidural bolus dose, followed by infusion of the assigned drug at 4ml per hour through BARD PCA I pump. Pain assessment, for the first four hours, was hourly, and subsequently at l0th, 16th, 22nd, 28th, 36th and 40th hour by VAS and VRS. The groups matched for demographic distribution. All groups had lower mean pain scores at first hour by VAS and VRS. In Group II and Group III, the difference was significant (<0.05) at the 2nd (VAS) and 4th (VRS) hours. From 16th (VAS) and 22nd (VRS) hours, the mean pain score was less and significant (<0.05) in Group III. In all groups sedation ranged from 0-1. There was hypotension in Group I (2/16).urinary retention in Group II (8/9 not catheterised); unilateral sensory impairment and motor weakness in Group I (3/16) and Group III (1/16). This study showed that co...
Results: Fifty two percent (primi) and 64% (multi) gravida in Group I and 8% in the Group II expe... more Results: Fifty two percent (primi) and 64% (multi) gravida in Group I and 8% in the Group II experienced good to excellent relief of back pain. Eight percent in primi and 12% in multigravida had no relief in Group I. Few had benefit in the second stage. The duration of labor was reduced by 120 minutes in multi and by 77 minutes in primigravida in group I (P value <0.001). There was no change in the intrapartum fetal heart rate in both the groups and none required immediate resuscitation.
Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdomin... more Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdominal surgery were grouped into sixteen each, on complaint of pain. They received an epidural bolus dose, followed by infusion of the assigned drug at 4ml per hour through BARD PCA I pump. Pain assessment, for the first four hours, was hourly, and subsequently at l0th, 16th, 22nd, 28th, 36th and 40th hour by VAS and VRS. The groups matched for demographic distribution. All groups had lower mean pain scores at first hour by VAS and VRS. In Group II and Group III, the difference was significant (<0.05) at the 2nd (VAS) and 4th (VRS) hours. From 16th (VAS) and 22nd (VRS) hours, the mean pain score was less and significant (<0.05) in Group III. In all groups sedation ranged from 0-1. There was hypotension in Group I (2/16).urinary retention in Group II (8/9 not catheterised); unilateral sensory impairment and motor weakness in Group I (3/16) and Group III (1/16). This study showed that co...
Principles of Anesthesia Equipment, 2016
Middle East journal of anaesthesiology, 2003
Middle East journal of anaesthesiology, 2004
Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdomin... more Forty eight ASA I or II patients of either sex between 20-70 years undergoing major upper abdominal surgery were grouped into sixteen each, on complaint of pain. They received an epidural bolus dose, followed by infusion of the assigned drug at 4ml per hour through BARD PCA I pump. Pain assessment, for the first four hours, was hourly, and subsequently at l0th, 16th, 22nd, 28th, 36th and 40th hour by VAS and VRS. The groups matched for demographic distribution. All groups had lower mean pain scores at first hour by VAS and VRS. In Group II and Group III, the difference was significant (<0.05) at the 2nd (VAS) and 4th (VRS) hours. From 16th (VAS) and 22nd (VRS) hours, the mean pain score was less and significant (<0.05) in Group III. In all groups sedation ranged from 0-1. There was hypotension in Group I (2/16).urinary retention in Group II (8/9 not catheterised); unilateral sensory impairment and motor weakness in Group I (3/16) and Group III (1/16). This study showed that co...
Journal of Pain and Symptom Management, 1997
Journal of Pain and Symptom Management, 1993
Journal of Pain and Symptom Management, 1994
Journal of Pain and Symptom Management, 1993
The Clinical Journal of Pain, 1993