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Dive into the research topics where Abhaya Gupta is active.

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Featured researches published by Abhaya Gupta.


Journal of Pediatric Surgery | 2010

Laparoscopic inguinal hernia repair in the pediatric age group—experience with 437 children

Sandesh V. Parelkar; Sanjay N Oak; Rahul Kumar Gupta; Beejal Sanghvi; Pradeep Shimoga; Deepak Kaltari; Advait Prakash; Raj Shekhar; Abhaya Gupta; Mitesh Bachani

BACKGROUND/PURPOSE A retrospective analysis of prospectively collected data of pediatric patients that underwent laparoscopic inguinal hernia repair. MATERIAL AND METHODS A retrospective review was performed of the prospectively collected data of 576 laparoscopic internal ring closures in 437 children (age, 30 days-11 years; median, 1.9 years) from June 1999 to February 2009. The internal ring was closed with a 3-0 nonabsorbable suture. Both extracorporeal and intracorporeal methods of knotting were used. All patients were asked to return at 1 week and 6 weeks postoperatively for routine follow-up. RESULTS A contralateral patent processus vaginalis was present in 13% (45/352) of boys and 15% (12/83) of girls on the right side, and 7% (25/352) of boys and 6% (5/83) of girls on the left side. Follow-up range was from 1 week postoperatively to 108 months. There were 14 recurrences (2.4 % [14/576], 11 in boys and on the right side and 3 in girls) and 2 hydroceles 0.35% (2/576). Mean operating time was 23 minutes for unilateral and 29 minutes for bilateral inguinal hernia. There was neither metachronus hernia nor testicular atrophy observed during follow-up. CONCLUSION Laparoscopic inguinal hernia repair is technically easier, as there is no need to dissect the vas deferens and vessels. The risk of metachronous hernia is reduced, and we believe the cosmetic result is better. Although recurrences were more common early in the series, currently they are much less frequent. Laparoscopic inguinal hernia repair appears to have less morbidity than open herniotomy and can be used as routine procedure in the pediatric age group.


Journal of Pediatric Surgery | 2009

Experience with video-assisted thoracoscopic removal of pulmonary hydatid cysts in children.

Sandesh V. Parelkar; Rahul Kumar Gupta; Hemanshi Shah; Beejal Sanghvi; Abhaya Gupta; Vinay Jadhav; Madhu Garasia; Amit Agrawal

Pulmonary hydatid disease is prevalent in many parts of world including India. In our small series of 5 pediatric patients, all patients were diagnosed with clinical and radiological findings on plain X-ray chest and CT (Computed Tomography) chest. All of them received oral albendazole 10 mg/kg/day soon after diagnosis except in one patient in which preoperative differential diagnosis was bronchogenic cyst and lung abscess (case 4). All underwent video assisted thoracoscopy. Simple endotracheal intubation was utilized in all cases along with CO(2) insufflation. Complete thoracoscopic removal was successful in 3 cases, while conversion to open thoracotomy was required in 2 cases. All of them showed rapid recovery except for one patient in whom prolonged intercostal drainage was present for 2 weeks. The average duration of procedure was 150 minutes and average length of hospital stay was 4.5 days except case 2, which was discharged on day 15 due to prolonged air leak. Histopathology in all cases was suggestive of hydatid cyst. At mean follow up of 6 months, all patients are asymptomatic and doing well.


Journal of Pediatric Urology | 2010

Urethral ratio on voiding cystourethrogram: A comparative method to assess success of posterior urethral valve ablation

Rahul Kumar Gupta; Hemanshi Shah; Vinay Jadhav; Abhaya Gupta; Advait Prakash; Bejal Sanghvi; Sandesh V. Parelkar

OBJECTIVE To develop a simple, objective and reproducible quantitative measurement to assess success of posterior urethral valve ablation. METHOD In 30 patients with posterior urethral valves the diagnosis was confirmed by voiding cystourethrogram (VCUG). Our protocol was to perform valve ablation, and repeat VCUG at 12 weeks postoperatively. Urethral ratio was calculated by dividing the posterior urethral diameter by the anterior urethral diameter. Thirty males undergoing VCUG for urinary tract infections were evaluated as normative controls. RESULTS Median age of controls was 12 months (2 days-6 years) and of study group was 13 months (1 day-11 years). Mean urethral ratio in pre-fulguration group was 4.94 (+/-2.97) and in post-fulguration group was 2.134 (+/-1.19) (P<0.001). The mean urethral ratio in the control group of 1.73 (+/-0.577) was significantly different from the pre-fulguration group result (P<0.001), but not significantly different in comparison to the post-fulguration group (P=0.104). CONCLUSION Calculation of urethral ratio on VCUG as a method of assessment of outcome of fulguration is objective, reproducible, and allows preoperative and postoperative VCUG from different facilities to be compared. A post-fulguration urethral ratio of 2.5-3 represents an acceptable result postoperatively.


Journal of Pediatric Surgery | 2008

Congenital alveolar fusion.

Rahul Kumar Gupta; Vinay Jadhav; Abhaya Gupta; Beejal Sanghvi; Hemanshi Shah; Sandesh V. Parelkar

Congenital fusion of the jaws is rare. It may be unilateral or bilateral and may involve only the soft tissues or both the hard and soft tissues. This anomaly may be seen separately or in association with other syndromes. Congenital alveolar fusion restricts mouth opening, causing problems with feeding, swallowing, and respiration. Case 1 had membranous bands between the alveoli that required tracheostomy for stabilization, followed by osteotomy for release. Postoperatively, both patients had adequate mouth opening.


European Journal of Pediatric Surgery | 2014

Closure of Large Meningomyelocele Wound Defects with Subcutaneous Based Pedicle Flap with Bilateral V-Y Advancement: Our Experience and Review of Literature

Krushnakumar Kesan; Paras Kothari; Rahul Gupta; Abhaya Gupta; Parag Karkera; Ritesh Ranjan; Kedar Mutkhedkar; Gurusev Sandlas

BACKGROUND Meningomyelocele is a defect of the spinal cord, vertebrae, and the overlying skin and is the most common form of open spinal dysraphism. Rapid closure of the back defect in the early postnatal period is mandatory to reduce the frequency of infection-related complications of the central nervous system. Majority of the cases present with small defects, which can be closed primarily, with or without subcutaneous dissection. However, direct closure is not possible in 25% of the cases. Different types of local flaps (skin or muscle flaps) are widely used for covering the skin defects; and with varying results. PATIENTS AND METHODS A prospective nonrandomized study was conducted in the department of pediatric surgery at a tertiary hospital, from September 2007 to October 2011. Overall 35 patients with large meningomyelocele defects that could not be closed primarily were included in the study. All patients were treated using subcutaneous tissue based pedicle flap with bilateral V-Y advancement. RESULTS There were 27 neonates, 7 infants, and 1 child, with a male:female ratio of 1.19:1. There were 3 thoracolumbar, 14 lumbar, 14 lumbosacral, 3 sacral, and 1 multiple meningomyelocele defects with an average size of 8.5 cm (range 6.5-11 cm). Average intraoperative blood loss was 8 mL (range 6-10.5 mL). Average operative time which included flap reconstruction time, after closure of dura, was 38.6 min. Total seven patients had wound complications viz. fat necrosis (n = 2), flap necrosis (n = 2), hematoma (n = 1), cerebrospinal fluid leak followed by wound dehiscence (n = 1), wound infection which led to meningitis (n = 1). Average healing time for flap repair was 7.52 days. Overall 80% (n = 28) of the patients had good flap texture and contour with satisfactory cosmesis. CONCLUSION Closure of large meningomyelocele wound defects with subcutaneous based pedicle flap with bilateral V-Y advancement is an effective technique. The main advantages of this technique are its simplicity, short operative time, good tolerance, early healing, and good cosmetic outcome with an excellent flap texture and contour match with minimal complications.


Indian Journal of Plastic Surgery | 2013

Gluteal flap for omphalocele repair in a case of epigastric heteropagus: A novel approach for surgical management

Krushnakumar Kesan; Abhaya Gupta; Rahul Kumar Gupta; Paras Kothari; Ritesh Ranjan; Parag Karkera; Kedar Mudkhedkar

Epigastric heteropagus is an extremely rare congenital anomaly, in which there is asymmetrical conjoined twinning, with the parasitic twin attached to the epigastrium. A 2-day-old male, with epigastric heteropagus and omphalocele, was operated in our institution. After excision of the parasitic twin, omphalocele was covered with a gluteal skin flap available from the parasitic twin. Post-operative course was uneventful, except for infection along the edges of the skin flaps, which was managed conservatively. Only 44 cases of epigastric heteropagus twins have been reported previously in world literature. We present a novel surgical approach for the repair of the omphalocele in a case of epigastric heteropagus twins, probably the 45th case to be reported in the world literature.


Journal of bronchology & interventional pulmonology | 2009

Subcutaneous emphysema: an unusual presentation of foreign body aspiration.

Rahul Kumar Gupta; Abhaya Gupta; Beejal Sanghvi; Sandesh V. Parelkar; Pankaj Mishra

Two cases of subcutaneous emphysema owing to foreign body aspiration are described. In case 1, a 2½-year-old boy presented with complaints of respiratory distress, cough, and swelling over neck. Computed tomography scan of neck and thorax revealed subcutaneous emphysema along with emphysematous changes of left lung. In Case 2, a 5-year-old boy presented with left pneumothorax along with massive subcutaneous emphysema, extending from the face to the chest. Computed tomography scan of the chest revealed subcutaneous emphysema, pneumomediastinum, and left pneumothorax. Both of the patients underwent bronchoscopic removal of the foreign body from the left main bronchus. At present both are asymptomatic and doing well. Subcutaneous emphysema is rare as a manifestation of foreign body aspiration and this cause should be kept in mind, even in the absence of forthcoming history of aspiration.


World Journal of Gastrointestinal Surgery | 2015

Thoracoabdominal pseudocyst of pancreas: An rare location, managed by retrocolic retrogastric Roux-en-Y cystojejunostomy

Ravikiran Shankar Kamble; Rahulkumar Gupta; Abhaya Gupta; Paras Kothari; K Vishesh Dikshit; Geeta Kekre; Prashant Patil

Pseudocyst formation is a common complication of acute and chronic pancreatitis. Most common site of pseudocyst is lesser sac; mediastinal extension of pseudocyst is rare. Other possibilities of posterior mediastinal cyst must be considered. This patient presented with computed tomography abdomen with thorax showing a large thoraco-abdominal pseudocyst with right sided pleural effusion. It was confirmed to be pancreatic pseudocyst by analyzing fluid for amylase and lipase during surgery. In our patient, the pseudocyst was accessible transabdominaly. Cystogastrostomy was not possible as it was causing twisting of cardio-esophageal junction; we did retrocolic and retrogastric Roux-en-Y cystojejunostomy. Only two such cases were reported in literature.


African Journal of Paediatric Surgery | 2009

Minimal access surgery in children: An initial experience of 28 months

Abhaya Gupta; Rahul Kumar Gupta; Vinay Jadhav; Beejal Sanghvi; Hemanshi Shah; Sv Parelkar

BACKGROUND This study reports our 28 months experience with minimal access surgery (MAS) in children. MATERIALS AND METHODS This was a review of all children who underwent MAS between December 2004 and March 2007 at the Departments of Paediatric Surgery, Seth Gordhandas Sunderdas Medical College (GSMC) and King Edward the VII Memorial (KEM) Hospital, India. Results and observations were tabulated and analysed, comparing with observations by various other authors regarding variety of indications such as, operative time, hospital stay, conversion rate, complications, safety, and feasibility of MAS in neonates, in the appropriate operative groups. RESULTS A total of 199 procedures were performed in 193 children aged between 10 days and 12 years (average age: 5.7 years). One case of each, adrenal mass, retroperitoneoscopic nephrectomy, laparoscopic congenital diaphragmatic hernia (CDH) repair, and abdominoperineal pull-through for anorectal malformation, were converted to open surgeries due to technical difficulty. The overall conversion rate was 3%. Morbidity and mortality were very minimal and the procedures were well tolerated in majority of cases. CONCLUSION We concluded that MAS procedures appear to be safe for a wide range of indications in neonates and children. Further development and expansion of its indications in neonatal and paediatric surgery requires further multi-institutional studies and larger cohort of patients, to compare with standards of open surgery.


Journal of Pediatric Neurosciences | 2016

Immediate and long-term outcome analysis of lipomeningomyelocele repair in asymptomatic infants in a tertiary care center.

Prashant Patil; Abhaya Gupta; Paras L Kothari; Geeta Kekre; Rahul Gupta; Vishesh Dikshit; Kedar Mudkhedkar; Krishna Kesan

Objective: To analyze immediate and long-term results of lipomeningomyelocele (LMM) repair in asymptomatic patients. Materials and Methods: Seventeen patients of LMM presented to Department of Paediatric Surgery over a period from 2011 to 2015 were evaluated preoperatively by magnetic resonance imaging of whole spine, and pre- and post-operative Ultrasound of kidney, ureter, bladder, and neurosonogram. Surgical procedure involved total excision of lipoma in 15 patients and near total excision in 2 patients. Division of filum terminale could be done in 15 out of 17 patients. Follow-up varied from 1 to 3.5 years (mean 1.9 years). Results: This study included 10 (58.8%) patients of lumbosacral LMM, 5 (29.4%) patients of sacral, and 2 (11.7%) patients of thoracolumbar LMM. About 13 (76.4%) patients were operated before 3 months of age, 2 (23.5%) patients were operated between 3 and 6 months, and two patients were operated between 6 and 11 months. None of the patients had bladder/bowel dysfunction preoperatively. Preoperative lower limb power was normal in all patients. Objective improvement in lower limb motor function was observed in 3 (17.6%) patients and three patients had decreased lower limb power. Two patients developed altered sensations and weakness of lower limb about 2.5-3 years after initial LMM repair. They needed repeat detethering of cord. Two patients had fecal pseudoincontinence, whereas one patient developed constipation. Bowel dysfunction was managed by rectal washouts, and oral laxatives were added if required. One (5.8%) patient of lumbosacral LMM and 1 (5.8%) patient of sacral LMM had urinary incontinence postoperatively. This was managed by clean intermittent catheterization with continuous overnight drainage. Conservative management of bladder and bowel dysfunction was effective in all patients till the last follow-up. Two patients developed hydrocephalus after LMM repair for which low-pressure ventriculoperitoneal shunt was inserted. Wound infection occurred in 1 (5.8%) patient, whereas 7 (41.1%) patients developed seroma in wound which responded to repeated aspirations under aseptic precautions. Conclusion: With total excision of lipoma and division of filum terminale satisfactory outcome for asymptomatic patients of LMM can be achieved. Authors recommend early surgery for LMM even in asymptomatic patients. Patients with residual lipoma and undivided filum terminale should be observed closely for the development of progressive neurological changes.

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Paras Kothari

Lokmanya Tilak Municipal General Hospital

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Geeta Kekre

Lokmanya Tilak Municipal General Hospital

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Rahul Kumar Gupta

King Edward Memorial Hospital

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Prashant Patil

Lokmanya Tilak Municipal General Hospital

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Kedar Mudkhedkar

Lokmanya Tilak Municipal General Hospital

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Rahul Gupta

Muljibhai Patel Urological Hospital

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Ritesh Ranjan

Lokmanya Tilak Municipal General Hospital

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Krushnakumar Kesan

Lokmanya Tilak Municipal General Hospital

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Parag Karkera

Lokmanya Tilak Municipal General Hospital

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Sandesh V. Parelkar

King Edward Memorial Hospital

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