22 results on '"Kubba, H."'
Search Results
2. O002 Medical therapy for sleep disordered breathing in children: a randomised, double-blind placebo-controlled trial
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Baker, A, Grobler, A, Davies, K, Griffiths, A, Hiscock, H, Kubba, H, Peters, R, Ranganathan, S, Rimmer, J, Rose, E, Rowe, K, Simpson, C, Davidson, A, Nixon, G, Perrett, K, Baker, A, Grobler, A, Davies, K, Griffiths, A, Hiscock, H, Kubba, H, Peters, R, Ranganathan, S, Rimmer, J, Rose, E, Rowe, K, Simpson, C, Davidson, A, Nixon, G, and Perrett, K
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Background Sleep Disordered Breathing (SDB) in children is characterised by snoring and breathing difficulties during sleep. Small clinical trials suggest intranasal corticosteroids reduce SDB severity as defined by polysomnography. We assessed the efficacy of intranasal corticosteroid for improving symptoms and quality of life (QOL) in children with SDB. Methods This is a double-blind, randomised, placebo-controlled trial of healthy children 3-12y referred to a specialist with SDB symptoms. Exclusions were previous adenotonsillectomy, obesity or severe SDB. Participants received daily intranasal mometasone furoate 50micrograms or normal saline for 6 weeks. The primary outcome was resolution of symptoms measured by SDB score. Secondary outcomes were SDB symptom scores, QOL, behaviour, parent and surgeon perceived need for surgery, and parent satisfaction with treatment. Results 276 participants were recruited; 138 in each group. 127 and 123 participants had primary outcome data at 6 weeks in the mometasone and saline groups respectively. Baseline age, atopic history, symptom severity and QOL were similar between groups. Resolution of SDB symptoms occurred in 44% [95%CI 35–53] of the mometasone group and 40% [95%CI 32–49] of the saline group; risk difference 4% [95%CI -0.8–16] p=0.511. Secondary outcomes were not different between groups. Discussion This large RCT, using clinical rather than polysomnographic outcomes to investigate the efficacy of mometasone on symptoms of SDB, found substantial rates of symptom resolution after 6 weeks in both groups. However, we found no difference in treatment effect between 6 weeks of intranasal mometasone over saline, for management of SDB symptoms in childhood.
- Published
- 2021
3. Trends in tonsillectomy surgery in children in Scotland 2000-2018
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Kubba, H, Downie, LS, Kubba, H, and Downie, LS
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BACKGROUND: Tonsillectomy is one of the most common surgical procedures in children but indications and surgical practice change over time. OBJECTIVES: We aimed to identify trends in tonsillectomy procedures in children, in particular the number of procedures performed, the age of child undergoing tonsillectomy and the type of hospital in which the surgery was performed. DESIGN: Review of Scottish Morbidity Records data (SMR01) which are routinely collected after everyday case procedure or overnight stay in all Scottish NHS hospitals. SETTING: All NHS hospitals in all 14 Scottish health boards. PARTICIPANTS: All children (0-16 years) undergoing tonsillectomy, 2000-2018. MAIN OUTCOME MEASURES: Number of tonsillectomy procedures; rate of tonsillectomy per 1000 children in the population; number of children aged 0-2 years and 3-4 years undergoing tonsillectomy; health board in which the surgery occurred; diagnostic coding for these episodes; length of stay and readmission within 30 days of surgery. RESULTS: During 2000-2018, there were 50,208 tonsillectomies performed in children in Scotland (mean 2642/year). The number of tonsillectomies per year remained constant (R = 0.322, P = .178) but tonsillectomies performed in children 0-2 years rose from 0.41 to 1.56 per 1000 (R = 0.912, P < .001), and 3-4 years from 3.06 to 6.93 per 1000 (R = 0.864, P < .001). The proportion of all children's tonsillectomies performed up to age 4 rose from 20.6% to 35.9% and up to age 2 from 2.4% to 8.1%. All specialist children's hospitals showed a significant increase in surgery in very young children. CONCLUSIONS: Tonsillectomy rates remained static between 2000 and 2018, despite a falling population. More tonsillectomies are now performed for obstructive sleep apnoea, at a young age and in regional children's hospitals. This has important implications for the workload of these specialist hospitals.
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- 2021
4. Exploring the Factor Structure of the Glasgow Children's Benefit Inventory: New Recommendations for Reporting Results
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Kubba, H, Whitmer, WM, Kubba, H, and Whitmer, WM
- Abstract
OBJECTIVE: Patient-reported outcomes can be useful for reporting benefit from non-life-saving interventions, but often they report a single overall score, which means that much information on the specific areas of benefit is lost. Our aim was to perform a new factor analysis on the Glasgow Children's Benefit Inventory (GCBI) to create subscales reflecting domains of benefit. Further aims were to assess the internal consistency of the GCBI, and to develop guidelines for reporting both a total score and sub-scales in future studies. METHODS: We collected 4 existing datasets of GCBI data from children who have undergone tonsillectomy, ventilation tube insertion, pinnaplasty, and submucous diathermy to the inferior turbinates. We performed exploratory factor analysis with principal axis factoring with varimax rotation, we sought redundancy in question items, and we measured internal consistency. RESULTS: Using the combined dataset of 772 cases, we found 4 factors which accounted for 64% of the variance and which we have labeled "Psycho-social," "Physical health," "Behavior," and "Vitality." Subscale results varied in predictable ways depending on the nature of the intervention. Cronbach's alpha was 0.928. Item-total correlations were high, and no item could be deleted to improve alpha. Floor effects were apparent for various questions but were not consistent between different interventions. CONCLUSIONS: The GCBI contains a range of questions which each add value in different clinical interventions. We can now make recommendations for reporting the results of the GCBI and its 4 new subscales.
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- 2021
5. Revised 15-item Glasgow Benefit Inventory with five factors based on analysis of a large population study of medical and surgical otorhinolaryngological interventions
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Browning, GG, Kubba, H, Whitmer, WM, Browning, GG, Kubba, H, and Whitmer, WM
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OBJECTIVES: To review, using confirmatory factor analysis, the widely used 18-question Glasgow Benefit Inventory [GBI] that has three factors. Thereafter to develop, using exploratory factor analysis, a more coherent, revised version of the GBI. DESIGN: Confirmatory and exploratory factor analysis of a large national GBI data set of ORL interventions. SETTING: Adult otorhinolaryngology outpatient clinics in six University Hospital departments. PARTICIPANTS: One thousand nine hundred eighty adult patients who had complete GBI data and who underwent an active (medical or surgical) intervention, out of the total data set of 9005 patients from the original Scottish ENT Outcome Study [SENTOS]. RESULTS: One of the 18 questions was discarded from the data base because it was not answered by 8% of respondents. Two of the original factors remained (Physical Health, renamed General Health, and Social Support, renamed Support). The General factor was split into three new factors (Quality of Life, Self-Confidence and Social Involvement). The three new factors were found to give additional information regarding the area of benefit. This reduced number of questions does not make any material difference to the results of the >196 existing GBI papers in the literature. CONCLUSION: A 15-question GBI with five factors is provided that is more explanatory of the areas of benefit.
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- 2021
6. Tonsillectomy and adenoidectomy in children with sleep-related breathing disorders: consensus statement of a UK multidisciplinary working party
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ROBB, P J, BEW, S, KUBBA, H, MURPHY, N, PRIMHAK, R, ROLLIN, A-M, and TREMLETT, M
- Published
- 2009
7. Our experience of a paediatrician-led clinic for the medical management of children with obstructive sleep-disordered breathing
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Kubba, H, Rowe, K, Pinczower, G, Sloane, R, Waterham, M, Weiss, E, Harwood, R, Kubba, H, Rowe, K, Pinczower, G, Sloane, R, Waterham, M, Weiss, E, and Harwood, R
- Abstract
BACKGROUND: Obstructive sleep-disordered breathing (OSDB) is very common in children. Adenotonsillectomy is usually curative, but there is emerging evidence that topical nasal steroids can also be effective for some children and may avoid the need for surgery. The number of children referred for assessment of OSDB is increasing and in some departments, waiting times are long. We established a paediatrician-led clinic for assessment and initial medical management of OSDB and in this study we report the proportion of children who avoided the need for surgery. METHOD: Referral letters to the otolaryngology department were screened and those with suspected OSDB and no significant co-morbidities were diverted to the paediatrician-led clinic. We recorded data for a consecutive series of children seen in this clinic with suspected OSDB over a 3-month period. Parents completed a 5-item subset of questions from the OSA-11 questionnaire before and after treatment with 6 weeks of topical nasal steroids. RESULTS: In the 3-month study period, 103 children were seen, with a mean age of 6 (range 1-16). Six (5.8%) had improved spontaneously before clinic attendance. Of the 97 children who were still symptomatic, 17 (17.5%) were referred directly for surgery on the basis of the severity of their symptoms, or because of other coexisting conditions that required surgical treatment (such as recurrent tonsillitis or otitis media). Three declined intranasal steroids. Seventy-seven had a trial of intranasal steroids, of whom 34 (35%) reported enough improvement to avoid surgery, and 29 (28%) failed to improve and were referred for surgery. Fourteen (14%) failed to attend after the trial of steroids: of these, 5 (5%) were contactable by phone and confirmed improvement after topical steroids. OSA-5 scores were significantly improved following intranasal steroids. DISCUSSION: A paediatrician-led clinic can be an effective way to ease the workload of an over-stretched otolaryngology service
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- 2020
8. Prevalence, risk factors and management strategies for otological problems in girls with Turner syndrome
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Lim, D, Hassani, S, Lupton, K, Gault, EJ, Wynne, D, Clement, W, Kubba, H, Mason, A, Donaldson, M, Lim, D, Hassani, S, Lupton, K, Gault, EJ, Wynne, D, Clement, W, Kubba, H, Mason, A, and Donaldson, M
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AIM: To determine the prevalence and risk factors of ear disease in Turner syndrome (TS), propose an algorithm for future surveillance and recommend preventative strategies. METHODS: Review of TS patients seen in the West of Scotland between 1989 and 2015, with questionnaire follow-up in 2015. RESULTS: Of 168 girls, median age 27.3 (3.8-47.2) years, ear problems occurred more frequently with 45,X and 45,X/46,XiXq than other karyotypes: 71/103 (69%) versus 23/65 (35%). Recurrent acute otitis media (AOM) first developed at 0-5 years in 23 (40%) girls, persisting in 16 (10%) at 5-10 years; and first developing at 5-10 years in 11 (7%). Persistent otitis media with effusion (OME) first developed at 0-5 and 5-10 years in 23 (40%) and 14 (8%) girls. Recurrent AOM was significantly linked with cholesteatoma in 8 (4.9%) girls (7 aged >10 years). Permanent hearing loss was documented in 28 girls (16.7%), with 16 (9.5%) receiving hearing aids (bone-anchored in 3). CONCLUSION: Acute otitis media and OME occur commonly in preschool TS girls and may persist or newly develop in later childhood. Recurrent AOM predisposes to cholesteatoma. Strategies to reduce otological morbidity include: intensive patient education, annual audiology, vaccinations and a randomised trial of antibiotic prophylaxis in high-risk groups.
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- 2020
9. Time to open our eyes? a challenge to the role of polysomnography for trials in pediatric sleep-disordered breathing.
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Perrett K.P., Nixon G.M., Kubba H., Perrett K.P., Nixon G.M., and Kubba H.
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- 2018
10. Meeting the challenges of acne treatment in Asian Patients: A review of the role of dermocosmetics as adjunctive therapy
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Goh, C. L., Noppakun, N., Micali, Giuseppe, Azizan, N., Boonchai, W., Chan, Y., Cheong, W., Chiu, P., Etnawati, K., Gulmatico, Flores, Foong, Z., Kubba, H., Paz, Lao, Lee, P., Loo, Y., Modi, S., Nguyen, F., Pham, T., Shih, T., Sitohang, Y., I. B., Wong, and S. N.
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medicine.medical_specialty ,lcsh:Surgery ,Alternative medicine ,MEDLINE ,Topical antibiotics ,Review Article ,Dermatology ,cosmeceuticals ,Appropriate use ,030207 dermatology & venereal diseases ,03 medical and health sciences ,0302 clinical medicine ,adjuvant ,medicine ,Acne ,Asian ,business.industry ,lcsh:RD1-811 ,Acne treatment ,medicine.disease ,030220 oncology & carcinogenesis ,Surgery ,dermocosmetics ,business ,Acne adjuvant Asian cosmeceuticals dermocosmetics - Abstract
Conventional acne treatment presents several challenges such as intolerable side effects and antibiotic resistance. Dermocosmetic products may be used to reduce these unwanted effects. Dermocosmetics include skin cleansers, topical sebum-controllers, skin antimicrobial/anti-inflammatory agents, moisturizers, sunscreens, and camouflage products. Appropriate use of these products may help augment the benefit of acne treatment, minimize side effects, and reduce the need for topical antibiotics. In Asia, there is currently limited scientific data on the application and recommendations for dermocosmetic use in acne vulgaris (AV). This article reviews the evidence on dermocosmetics for AV and provides practice recommendations as discussed during the 4(th) Asia-Pacific Acne Leaders' Summit held in Bangkok, Thailand, on 7 and 8 February 2015. Through a premeeting survey, a series of plenary lectures, a stepwise program of discussion sessions, and Medline article review, the Expert Panel set forth relevant recommendations on the role of dermocosmetics as adjunct for treating AV in Asian patients.
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- 2016
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11. Hormonal contraception prior to in vitro fertilization (IVF) adversly affects functional ovarian reserve and oocyte yields
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Gleicher, N., primary, Kubba, H., additional, and Weghofer, A., additional
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- 2011
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12. Paediatric obstructive sleep apnoea
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Powell, S., primary, Kubba, H., additional, O'Brien, C., additional, and Tremlett, M., additional
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- 2010
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13. Comparison of case note review methods for evaluating quality and safety in health care
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Lock, C, primary, Wilson,, J, additional, Steen, N, additional, Eccles, M, additional, Mason, H, additional, Carrie, S, additional, Clarke, R, additional, Kubba, H, additional, Raine, C, additional, Zarod, A, additional, Brittain, K, additional, Vanoli, A, additional, and Bond, J, additional
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- 2010
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14. 'Reflections' on an interesting case: an oropharyngeal foreign body presenting as cleft palate
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Fraser, L, primary and Kubba, H, additional
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- 2009
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15. Autoinflation for treatment of glue ear
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Kubba, H., primary, Reidpath, D. D, additional, Glasziou, P. P, additional, and Del Mar, C., additional
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- 1999
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16. Influence of using high volume fraction of silica fume on mechanical and durability properties of cement mortar
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Mohammed Nasr, Hussain, T. H., Kubba, H. Z., and Shubbar, A. A.
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TA ,technology, industry, and agriculture - Abstract
The high pollution caused by CO2 emission and the high level of energy consumed during cement manufacturing led the researchers to look for alternative techniques to reduce these environmental effects. One of these techniques includes reducing the content of cement in the mix by replacing it with supplementary cementitious materials such as fly ash, slag, silica fume, and so on. Many previous studies dealt with the utilizing of the high volume of supplementary cementitious materials, such as fly ash and slag. However, limited studies investigated the impact of silica fume on mortar or concrete properties in percentages of more than 30%. Thus, to produce environmentally friendly concrete, this study was performed to investigate the effect of the high replacement level of cement with silica fume on the properties of cement mortar. Six replacement proportions of silica fume (0%, 30%, 40%, 50%, 60% and 70%) were used in this paper. This paper used the flow rate, compressive strength, water absorption, bulk density and volume of permeable voids tests to test the effect of silica fume on different mortar characteristics. The results indicated that the best mixture among all other mixes was found by 50% substitution of silica fume. At this percentage, an enhancement in compressive strength of nearly 83%, 74% and 75% at 7, 28 and 56 days, respectively and an improvement in water absorption resistance by 8% compared to the control mixture were achieved.
17. Time to Open Our Eyes? A Challenge to the Role of Polysomnography for Trials in Pediatric Sleep-Disordered Breathing.
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Nixon GM, Kubba H, and Perrett KP
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- Child, Humans, Adenoidectomy, Polysomnography methods, Sleep Apnea Syndromes diagnosis, Sleep Apnea Syndromes surgery, Tonsillectomy
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- 2018
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18. Mechanical behaviour of biodegradable AZ31 magnesium alloy after long term in vitro degradation.
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Adekanmbi I, Mosher CZ, Lu HH, Riehle M, Kubba H, and Tanner KE
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- Corrosion, Magnesium, Materials Testing, Polymers, Prostheses and Implants, Alloys chemistry
- Abstract
Biodegradable magnesium alloys including AZ31 are exciting candidates for temporary implants as they eliminate the requirement for surgical removal, yet have higher mechanical properties than degradable polymers. However, the very long term mechanical properties and degradation of these alloys have not been fully characterized. The tensile, bending and corrosion behaviour of biodegradable AZ31 Mg alloy specimens have been investigated for up to 9months in vitro in phosphate buffered saline (PBS). Small AZ31 Mg specimens showed a significant drop in bend yield strength and modulus after 3months in vitro degradation and an average mass loss of 6.1%. Larger dumbbell specimens showed significant drops in tensile strength from 251.96±3.53MPa to 73.5±20.2MPa and to 6.43±0.9MPa and in modulus from 47.8±5.6GPa to 25.01±3.4GPa and 2.36±0.89GPa after 3 and 9months respectively. These reductions were accompanied by an average mass loss of 18.3% in 9months. Degradation rate for the small and large specimens followed similar profiles with immersion time, with peak degradation rates of 0.1747gm
-2 h- 1 h-2 h- h1 , and average rates of 0.1038gm-2 h- 1 and 0.0397gm-2 h- 1 respectively. SEM fractography and polished specimen cross-sections revealed corrosion pits, cracks and corrosion induced defects. These data indicate the potential of AZ31 Mg for use in implants that require medium term degradation with load bearing mechanical properties., (Copyright © 2017 Elsevier B.V. All rights reserved.)- Published
- 2017
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19. Does hormonal contraception prior to in vitro fertilization (IVF) negatively affect oocyte yields? A pilot study.
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Barad DH, Kim A, Kubba H, Weghofer A, and Gleicher N
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- Adult, Anti-Mullerian Hormone metabolism, Female, Humans, Oocytes cytology, Oocytes metabolism, Ovary cytology, Ovary drug effects, Ovary metabolism, Ovulation Induction methods, Ovulation Induction statistics & numerical data, Pilot Projects, Retrospective Studies, Time Factors, Young Adult, Contraceptives, Oral, Hormonal administration & dosage, Fertilization in Vitro, Oocytes drug effects, Progestins administration & dosage
- Abstract
Background: As oral contraceptives (OCs) suppress anti-Müllerian hormone (AMH), and hormonal contraceptives (HCs), likely, suppress functional ovarian reserve, this study was initiated to determine whether HC affect oocyte yields., Methods: We investigated in a retrospective cohort study 43 oocyte donors in 71 in vitro fertilization (IVF) cycles, evaluating anti-Müllerian hormone (AMH) and oocyte yields as reflections of functional ovarian reserve (OR). In 25 IVF cycles egg donors were on HC within one month prior to IVF, and in 46 cycles they were not. Donors, based on their HCs, were further subdivided into 12 with less, and 13 with more androgenic progestins., Results: While the three groups did not differ in age, age at menarche, BMI and AMH, oocyte yields among donors who utilized estrane- and gonane-derived (higher androgenic) HCs were lower 11.3 (95% CI 8.3 - 14.3) than either donors using no HCs 16.6 (95% CI 14.7 -18.4) (P < 0.05) or those using anti-androgenic HCs 19.0 (95% CI 12.2-25.8) (P< 0.01). Significance was maintained after adjustments for the donor age and total FSH dose used in ovulation induction., Conclusions: Even in young oocyte donors, high androgenic OC exposure appears to suppress functional ovarian reserve and oocyte yields. Since OCs are often routinely used in preparation for IVF, such practice may require reevaluation. Especially in women with diminished ovarian reserve OCs, and especially high androgenic progestin HCs, should, likely, be avoided.
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- 2013
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20. Coblation adenotonsillectomy in children.
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Shakeel M, Trinidade A, Al-Adhami A, Supriya M, and Kubba H
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- Ablation Techniques adverse effects, Ablation Techniques methods, Child, Child, Preschool, Female, Humans, Length of Stay, Male, Pain Measurement, Pain, Postoperative diagnosis, Pakistan epidemiology, Regression Analysis, Retrospective Studies, Treatment Outcome, Adenoidectomy methods, Pain, Postoperative epidemiology, Patient Readmission statistics & numerical data, Postoperative Hemorrhage epidemiology, Tonsillectomy methods, Tonsillitis surgery
- Abstract
Objective: To determine re-admission rate for post-tonsillectomy pain; the primary and secondary post-tonsillectomy bleeding rate; the percentage requiring control of post-tonsillectomy bleeding in children undergoing coblation tonsillectomy., Study Design: A descriptive study., Place and Duration of Study: Royal Hospital for Sick Children (Yorkhill Hospital) between 2004 and 2006., Methodology: All patients who underwent tonsillectomy with or without adenoidectomy by coblation technique. Patients were identified from operation theatre log book and electronic data base of theatre activity. The hospital case notes were reviewed retrospectively to collect data, regarding demographics, indication and type of surgery, grade of operating surgeon, duration of hospital stay, re-attendance and re-admission, and management of complications., Results: A total of 106 children; males (n = 53, 50%), females (n = 53, 50%) with a mean age 6.3 years underwent surgery using coblation technique. Thirty-one percent had a tonsillectomy while 69% underwent an adenotonsillectomy. Of these, 48% had history of recurrent tonsillitis, 43% had obstructive sleep apnoea and 9% suffered predominantly from obstructive symptoms. Eighty-two percent of patients were discharged on the first postoperative day. Only one patient had primary bleeding requiring re-operation. After discharge, 7 patients (6.7%) were re-admitted with secondary bleeding, 3 (2.8%) of whom were taken back to theatre to control the bleeding under general anaesthesia., Conclusion: Coblation tonsillectomy is a useful technique in having a low primary and secondary bleeding rates in children undergoing tonsillectomy and adenotonsillectomy.
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- 2012
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21. North of England and Scotland Study of Tonsillectomy and Adeno-tonsillectomy in Children(NESSTAC): a pragmatic randomised controlled trial with a parallel non-randomised preference study.
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Lock C, Wilson J, Steen N, Eccles M, Mason H, Carrie S, Clarke R, Kubba H, Raine C, Zarod A, Brittain K, Vanoli A, and Bond J
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- Adolescent, Child, Child, Preschool, Cohort Studies, Costs and Cost Analysis, England, Female, Financing, Personal, Humans, Interviews as Topic, Male, Scotland, Tonsillectomy economics, Adenoidectomy methods, Tonsillectomy methods
- Abstract
Objectives: To examine the clinical effectiveness and cost-effectiveness of tonsillectomy/adeno-tonsillectomy in children aged 4-15 years with recurrent sore throats in comparison with standard non-surgical management., Design: A pragmatic randomised controlled trial with economic analysis comparing surgical intervention with conventional medical treatment in children with recurrent sore throats (trial) and a parallel non-randomised cohort study (cohort study)., Setting: Five secondary care otolaryngology departments located in the north of England or west of Scotland., Participants: 268 (trial: 131 allocated to surgical management; 137 allocated to medical management) and 461 (cohort study: 387 elected to have surgical management; 74 elected to have medical management) children aged between 4 and 15 years on their last birthday with recurrent sore throats. Participants were stratified by age (4-7 years, 8-11 years, 12-15 years)., Interventions: Treatment was tonsillectomy and adeno-tonsillectomy with adenoid curettage and tonsillectomy by dissection or bipolar diathermy according to surgical preference within 12 weeks of randomisation. The control was non-surgical conventional medical treatment only., Main Outcome Measures: The primary clinical outcome was the reported number of episodes of sore throat in the 2 years after entry into the study. Secondary clinical outcomes included: the reported number of episodes of sore throat; number of sore throat-related GP consultations; reported number of symptom-free days; reported severity of sore throats; and surgical and anaesthetic morbidity. In addition to the measurement of these clinical outcomes, the impact of the treatment on costs and quality of life was assessed., Results: Of the 1546 children assessed for eligibility, 817 were excluded (531 not meeting inclusion criteria, 286 refused) and 729 enrolled to the trial (268) or cohort study (461). The mean (standard deviation) episode of sore throats per month was in year 1 - cohort medical 0.59 (0.44), cohort surgical 0.71 (0.50), trial medical 0.64 (0.49), trial surgical 0.50 (0.43); and in year 2 - cohort medical 0.38 (0.34), cohort surgical 0.19 (0.36), trial medical 0.33 (0.43), trial surgical 0.13 (0.21). During both years of follow-up, children randomised to surgical management were less likely to record episodes of sore throat than those randomised to medical management; the incidence rate ratios in years 1 and 2 were 0.70 [95% confidence interval (CI) 0.61 to 0.80] and 0.54 (95% CI 0.42 to 0.70) respectively. The incremental cost-effectiveness ratio was estimated as 261 pounds per sore throat avoided (95% confidence interval 161 pounds to 586 pounds). Parents were willing to pay for the successful treatment of their child's recurrent sore throat (mean 8059 pounds). The estimated incremental cost per quality-adjusted life-year (QALY) ranged from 3129 pounds to 6904 pounds per QALY gained., Conclusions: Children and parents exhibited strong preferences for the surgical management of recurrent sore throats. The health of all children with recurrent sore throat improves over time, but trial participants randomised to surgical management tended to experience better outcomes than those randomised to medical management. The limitations of the study due to poor response at follow-up support the continuing careful use of 'watchful waiting' and medical management in both primary and secondary care in line with current clinical guidelines until clear-cut evidence of clinical effectiveness and cost-effectiveness is available., Trial Registration: Current Controlled Trials ISRCTN47891548.
- Published
- 2010
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22. "Reflections" on an interesting case: an oropharyngeal foreign body presenting as cleft palate.
- Author
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Fraser L and Kubba H
- Published
- 2009
- Full Text
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