Abstract
Background and aims. There are several known sedative drugs, with midazolam and ketamine being the most commonly used drugs in children. The aim of this study was to compare the effect of intranasal and oral midazolam plus ketamine in children with high levels of dental anxiety.
Materials and methods. A crossover double-blind clinical trial was conducted on 23 uncooperative children aged 3-6 (negative or definitely negative by Frankel scale), who required at least two similar dental treatment visits. Cases were ran-domly given ketamine (10 mg/kg) and midazolam (0.5 mg/kg) through oral or intranasal routes in each visit. The sedative efficacy of the agents was assessed by an overall success rate judged by two independent pediatric dentists based on Houpt's scale for sedation. Data analysis was carried out using Wilcoxon test and paired t-test.
Results. Intranasal administration was more effective in reduction of crying and movement during dental procedures com-pared to oral sedation (P<0.05). Overall behavior control was scored higher in nasal compared to oral routes at the time of LA injection and after 15 minutes (P<0.05). The difference was found to be statistically significant at the start and during treatment. However, the difference was no longer significant after 30 minutes, with the vital signs remaining within physio-logical limits. Recovery time was longer in the intranasal group (P<0.001) with a more sleepy face (P=0.004).
Conclusion. Intranasal midazolam/ketamine combination was more satisfactory and effective than the oral route when sedating uncooperative children.
Key words: Anxiety, intranasal, ketamine, midazolam, oral sedation.
Introduction
One of the most common challenges faced by pediatric dentists in daily practice is child be-havior management. Any impression from a dental experience will be reflected through individual's fu-ture dental attendance by creation of positive or negative memories.1 Various approaches have been identified to enable the operator to overcome behav-ioral problems in children. However, in those with absolute negative behavior, help is necessary to achieve a successful procedure. Even an experienced pediatric dentist may find it difficult to render treat-ments to certain children when using conventional techniques. In these circumstances the use of con-scious sedation and general anesthesia (GA) is con-sidered as helpful alternatives.2
It is also important to note that because of the changes in society and the population's attitude to-ward interaction with children, older methods of physical restraints such as HOME (hand over mouth exercise) or the use of other physical restraints have lower credibility. In fact, such applications are only limited to certain cases with GA/sedation medical contraindications. Alternative methods of conscious sedation and general anesthesia are ways to over-come the behavioral problems. Several methods have been introduced in this regard, including topical, sublingual, intranasal, rectal, intracutaneous, subcu-taneous, intramuscular, intravenous and inhalation routes.3 It is important to note that each route has its advantages and disadvantages and could not be con-sidered for every case at every clinical situation.4 An example of limitations is the problem with initiation of sedation effect in oral sedation. The oral sedation onset time is long (delayed), while the drug's absorp-tion level is somehow unreliable. Another major is-sue in oral sedation is lack of titration capacity and its long-lasting effect delaying patient's discharge.3 On the other hand, intranasal sedation is a more re-cent approach which is considered as one of the al-ternate ways for prescribing certain medications to the existing oral technique. Intranasal sedation is known as a non-invasive way of drug administration, which is safe and is tolerated by children, with direct absorption potential of the sedative agent into the bloodstream without entering the liver and stomach. It also saves the fearful child from receiving more injections. The level of drug's absorption is almost similar to that of the IV sedation with peak plasma levels being reached in approximately 10 minutes.5-6
For long, conscious sedation has been considered as one of the most reliable alternatives to overcome high levels of interfering dental anxiety with accept-able levels of health and safety of the patient when used by skilled pedodontists. Midazolam and keta-mine are two well known sedative drugs with unique characteristics.7 Bahetwar et al8 showed that keta-mine and midazolam are safe and efficient separately and in combination (success rates of 89%, 69% and 84%, respectively). Oral sedation has been satisfacto-rily achieved by the administration of chloral hydrate and hydroxizine in children.9 Submucosal meperi-dine has also been successfully tested in pediatric dental sedation.10
Lee-Kim11 compared the intranasal (IN) sedation of midazolam (0.3 mg/kg) and peroral (PO) mida-zolam (0.7 mg/kg) in pediatric dentistry. The chil-dren's general behavior were shown to be similar in both IN and PO sedation while more child move-ment and less drowsiness were reported in IV seda-tion.
The aim of this study was to compare the efficacy and safety of intranasal midazolam/ketamine combi-nation with oral methods along with N2O in sedating children for dental procedures.
Materials and Methods
This randomized crossover double-blind clinical trial (IRCT ID: IRCT201305101882N3) was conducted on 23 children aged 3-6, who were referred to the Department of Pediatric Dentistry, Shahid Beheshti Dental School, Tehran, Iran. Uncooperative 3-6-year-old children with negative and definitely nega-tive Frankel scale in ASA I or II were included in this dental treatment process under conscious seda-tion.3 Cases with at least two similar treatment needs were booked for two separate sessions needing pul-potomy with SSC or restoration. Exclusion criteria were any systemic disease, allergy to drugs, colds, nasal obstruction, respiratory infections, limited neck movement, macroglossia, tonsillar hypertrophy and microglossia. A written informed consent was sought from each patient's parents with full pre-sedation instructions. All the steps of sedation were per-formed under the direct supervision of an anesthesi-ologist. Major vital signs of SPO2 respiratory rate and BP were recorded at the start, middle and end of the treatment session. All the children were re-quested to be kept at NPO status for 6 hours (solid foods) and 4 hours (water and liquids) preopera-tively. The children were randomly assigned to two groups for the starting technique of A: intranasal se-dation and B: oral sedation. A questionnaire was used to record medical and dental histories. For seda-tion preparation in group A, 1 mL of 2% lidocaine hydrochloride (Pasteur Industrial Co, Iran) was add- ed to 0.25 mg/kg of atropine (Abu Reyhan Pharma-ceutics Co., Tehran, Iran). This combination was then dropped into the nostril mucosa using a 2-mL syringe. A second combination was an 0.5-mg/kg midazolam vial (Chemidaru Industrial Co., Tehran, Iran) added to 10 mg/kg of ketamine (Chemidaru Industrial Co., Tehran, Iran) before being dropped into the nostrils, 5 minutes after the administration of the initial drugs.
The second group received 0.5 mg/kg of oral mi-dazolam (Amsed Syrup, Dales Pharmaceuticals, Skipton, North Yorkshire, UK) along with 10 mg/kg of ketamine and 0.25 mg/kg of atropine in a cup or syringe. Both groups received the alternate treatment protocol during their second session. This was aimed to have every child serve as his or her own control. A local anesthetic was obtained using a 2% lidocaine hydrochloride cartridge with 1:80000 epinephrine (Darupakhsh Pharmaceutical MFG, Co., Iran). Den-tal treatments were carried out by a pedodontist blinded to the type of the medications administered. The sedative effect of the drugs was measured after 40 and 15 minutes of oral and nasal administrations, respectively. Dissociative state induced by ketamine sedation was judged by semi-closed eyes and nys-tagmus. A standard flow of N2O (40%) and O2 was administered for all the patients throughout the treatment courses.
Oxygen saturation was monitored at various steps of the study starting with premedication time at base-line using a multipurpose monitoring unit (Saadat Co, Iran).
All the measurements were made at baseline, at the local anesthetic injection, and 15 and 30 minutes af-ter the start of dental treatment. Houpt Scale was used to record every change in child's behavior with the following criteria: the amount of crying (C), sleeping (S) and movement (M) and overall behavior (O).6,12 Video recordings were also scheduled for the entire treatment sessions, which were subjected to evaluation and scoring by an independent pediatric dentist blinded to the administration of drugs. In case of poor cooperation, further sedative drugs were ad-ministered if needed in order to complete the treat-ment process while the least score was recorded for the case and sedation technique. Attempts were made to limit each treatment session to a maximum of 35 minutes.
The children were discharged when full conscious-ness was achieved as judged by the anesthesiologist and all vital signs returned to normal ranges. The parents were interviewed 24 hours after each session to respond to a series of questions in the patient's form in relation to postoperative complications. Data were analyzed using Wilcoxon test and paired t-test.
Results
Data from all the 23 children (18 boys, 5 girls), aged 3-6, were recorded. An initial behavior rating scale (Frankel scale) evaluation revealed that 21 cases (91.3%) were completely negative while 2 (8.7%) cases were judged to be negative. Overall no signifi-cant differences were found between the oral and nasal sedation with the drugs administered.
Comparison of sleep (S), movement (M), crying (C) and overall behavior (O) parameters showed sig-nificant differences between oral and nasal groups at LA injection time and after 15 minutes (P<0.05) in favor of intranasal sedation. However, these differ-ences were not found to be significant after 30 min-utes.
As detailed in the "Materials and Methods" sec-tion, all the participants were selected from those classified as definitely negative with the drug ad-ministration being carried out by force in both ses-sions. Since each patient served as control, compari-son of the outcomes showed little or no difference in drug acceptance rates. The success rates of oral and nasal administrations at different measured steps showed that the difference was statistically signifi-cant after 15 and 30 minutes (P<0.05). These meas-ures were 96.6% and 60.9% for nasal sedation after 15 and 30 minutes versus 39.1% and 34.7% for oral sedation at two occasions, respectively.
According to parents, the most common complica-tions after the treatment were nausea, vomiting, drowsiness and reduction of activity during the ini-tial 24 hours of both oral and nasal sedation sessions.
Recovery time was shorter in oral sedation (1 hour) compared to nasal approach (2.5 hours), indi-cating a significant difference (P<0.05) between the two.
There was no significant difference between nasal and oral sedation sessions when dental operation was judged. Likewise 87% of parents had a similar im-pression with little or no difference between the two sedation techniques and sessions. Maximum drowsi-ness was reported as lasting just under 2 hours fol-lowing oral intake while this was 4-6 hours in the nasal group with the difference as being statistically significant (P=0.004).
There were no statistically significant differences between the two sedation groups in their heart rates (HR), SPO2, RR, and maximum and minimum BP changes.
Discussion
Based on the results of this investigation there is a promising potential for the use of sedation tech-niques to overcome children's interfering behaviors in the dental office. Both intranasal and oral seda-tions could provide certain levels of calmness for the child and dentist while a dental procedure is under-way. Among the two techniques of sedation, it ap-pears that the intranasal method provided a higher and more satisfactory sedation rate, however this difference was not statistically significant. These results enhanced the idea that although behavior management techniques are considered useful tools in controlling most of the uncooperative children, the remaining cases who do not respond to these tech-niques could benefit from pharmacological aids. These may include various conscious sedation tech-niques to even full general anesthesia for single-visit full-mouth dental treatment.8
Oral sedation is the most common yet easily ac-cepted technique among the various routes of seda-tion in children. However, delayed onset is consid-ered as the main disadvantage of oral sedation in ad-dition to a long recovery period and high first pass metabolism.5,9 The highest level of effect is usually reached after 40-60 minutes of drug administration.5
Intranasal administration involves a path in which the drug is administered, aiming to have an immedi-ate absorption into the bloodstream, because of high vascularity of nasal mucosa and increased drug bioavailability without first pass metabolism effect. The technique is simple and effective and requires minimal cooperation.4,5,13
In these lines midazolam is considered as the most popular medication which like other benzodiazepines exhibits several positive effects, including hypnotic sedation, amnesia, muscle relaxation and relief of anxiety. Its ability to create anterograde amnesia is much higher when compared to other benzodiazepi-nes.14 Higher bioavailability and quicker onset have been demonstrated for intranasal midazolam admini-stration.8,15
Ketamine is also another widely used sedative drug with unique properties, including cataleptic condi-tion, amnesia and respiratory and cardiac stability. Its lower doses are routinely used as a sedative in many medical and dental diagnostic and therapeutic procedures.16,17
Additional administration of N2O-O2 alongside benzodiazepines in the form of a cocktail could boost the sedative outcome during child's dental visit while maintains adequate oxygen levels.18-20 Optimal dose for oral ketamine is indicated as 3-10 mg/kg with 0.2-0.75 mg/kg of midazolam in children.5 Mil-ler21 recommended 6-10 mg/kg of oral and 5-6 mg/kg of nasal ketamine as the safe and effective dose.
Gharde et al22 successfully used 10 mg/kg of keta-mine and 0.2 mg/kg of midazolam in combination with 0.1 mg/kg of midazolam and 7.5 mg/kg of ke-tamine intranasally for premedication of children with Tetralogy of Fallot. Tszeet al23 evaluated the effect of nasal doses of 3, 6 and 9 mg/kg of ketamine for pediatric sedation in wound healing and reported no sufficient sedation being achieved when INK doses below 6 mg/kg were used. It was concluded that 9 mg/kg of nasal ketamine is capable of provid-ing 95% sedation rate needed for most of the dental processes. Combination of midazolam and ketamine as oral or nasal medication have been reported to boost the results. Vahid et al24 compared oral mida-zolam (0/4 mg/kg)-ketamine (5 mg/kg) and mida-zolam (0/5 mg/kg)-promethazine (5 mg/mL) as sedative agents and concluded that keta-mine/midazolam combination could sufficiently se-date children even in lower doses, unlike mida-zolam/promethazine combination used in their study.
Bahetwar et al8 compared nasal ketamine and mi-dazolam and their combination with success rates of 98%, 69% and 89%, respectively. It is evident that such nasal combinations could induce moderate se-dation, with midazolam remaining to be the weakest when administered alone. In contrast, Lee-Kim11 showed no significant differences between the suc-cess rates of oral and nasal midazolam. Fuks25 com-pared intranasal 0.2 and 0.3 mg/kg midazolam and showed no significant differences between the out-comes achieved from the doses tested with a gener-ally successful sedation effect achieved, similar to the findings of the current study.
Diaz26 reported no nausea and vomiting following the administration of ketamine and placebo, with no post-sedation complications being reported in this investigation with the use of similar sedative agents. No significant differences were noted in the level of cases with nausea, vomiting, headache of the two groups tested. Damle et al15 reported higher levels of nausea following the use of ketamine than when mi-dazolam was used.
Ketamine is an analgesic while midazolam is an anti-anxiety and sedative agent but lacks any analge-sic effects. In addition to the use of any sedative drugs, the use of local anesthesia is essential for most of the dental treatments.8,11,24,27 Postoperative sleep phase was 0-1 hour for oral sedation with 2-3 hours for intranasal sedations at the recovery stage, with statistically significant differences.
Conclusion
1. The combination of intranasal ketamine-midazolam produced a more satisfactory level of sedation in children for short dental procedures (35 minutes) compared to that of oral route based on Houpt Scales.
2. The differences in the overall sedation levels achieved were statistically significant at 15- and 30-minute intervals.
Acknowledgments
The authors would like to thank the generous scien-tific and financial support and help of Dental Re-search Center, Research Institute of Dental Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
References
1. Hosey MT. Anxious Children: Coping in dental practice. Dental Update 1995;22:210-5.
2. Lökken P, Bakstad OJ, Fonnelöp E, Skogedal N, Hellsten K, Bjerkelund CE, et al. Conscious sedation by rectal admini-stration of midazolam or midazolam plus ketamine as alter-native to general anesthesia for dental treatment of uncoop-erative children. Scand J Dent Res 1994;102:274-80. doi: 10.1111/j.1600-0722.1994.tb01468.x
3. Malamed SF. Sedation: A Guide to Patient Management; The Spectrum of Pain and Anxiety Control, 5th ed. China: El-sevier; 2010. p. 14-22.
4. Safranek DJ, Eisenberg MS, Larsen MP. The epidemiology of cardiac arrest in young adult. Ann Emerg Med 1992;21:1102-6.
5. Malamed SF. Sedation: A Guide to Patient Management. Oral Sedation, 5th ed. China: Elsevier; 2010.p. 95-118.
6. Primosch RE, Guelmann M. Comparison of drops versus spray administration of intranasal midazolam in two-and three-year-old children for dental sedation. Pediatr Dent 2005;27:401-8.
7. Roelofse JA. What's new in paediatric conscious sedation in dentistry? SAAD Dig 2010; 26: 3-7.
8. Bahetwar SK, Pandey RK, Saksena AK, Chandra G. A com-parative evaluation of intranasal midazolam, ketamine and their combination for sedation of young uncooperative pedi-atric dental patients: a triple blind randomized crossover trial. J Clin Pediatr Dent 2011;35:415-20. doi: 10.17796/jcpd.35.4.l43h3354705u2574
9. Fallahinejad Ghajari M, Vahid Golpayegani M, Bargrizan M, Ansari G, Shayeghi S. Sedative effect of oral mida-zolam/hydroxyzine versus chloral hydrate/hydroxyzine on 2-6 year-old uncooperative dental patients: a randomized clinical trial. J Dent (Tehran) 2014;11:93-9.
10. Toomarian L, Salem K, Ansari G, Assessing the sedative effect of oral vs submucosal meperidine in pediatric dental patients. Dent Res J (Isfahan) 2013;10:173-9. doi: 10.4103/1735-3327.113335
11. Lee- Kim SJ, Fadavi S, Punwani I, Koerber A. Nasal versus oral midazolam sedation for pediatric dental patient. J Dent Child(Chic) 2004;71:126-30.
12. Houpt MI, Weiss NJ, Koenigsberg SR, Desjardins PJ: Com-parison of chloral hydrate with and without promethazine in the sedation of young children. Pediatr Dent 1985;7:41-6.
13. Hossain AA. Mechanism of nasal absorption of drugs. Prog Clin Biol Res 1989;292:261-72.
14. Bhatangar S, Mishra S, Gupta M, Srikanti M, Mondol A, Diwedi A. Efficacy and safety of a mixture of ketamine, mi-dazolam and atropine for procedural sedation in pediatric oncology: a randomized study of oral versus intramuscular-route. J Pediatr Child Health 2008;44:201-4. doi: 10.1111/j.1440-1754.2007.01233.x
15. Damle SG, Gondhi M, Laheri V. Comparison of oral keta-mine and oral midazolam as sedative agents in pediatric den-tistry. J Indian Soc Pedo Prev Dent 2008;26:97-101. doi: 10.4103/0970-4388.43186
16. Grant IS, Nimmo WS, Clement JA. Pharmacokinetics and analgesic effects of i.m. and oral ketamine. Br J Anaesth 1981;53:805-10. doi: 10.1093/bja/53.8.805
17. Weksler N, Ovadia L, Muati G, Stav A. Nasal ketamine for pediatric premedication. Can J Anaesth 1993;40:119-21. doi: 10.1007/bf03011307
18. Lam C, Udin RD, Malamed SF, Good DL, Forrest JL. Mida-zolam premedication in children: a pilot study comparing in-tramuscular and intranasal administration. Anesth Prog 2005;52:56-61. doi: 10.2344/0003-3006(2005)52%5B56:mpicap%5D2.0.co;2
19. Mathai A, Nazareth M, Rinu RS. Preanesthetic sedation of preschool children: Comparison of intranasal midazolam versus oral promethazine. Anesth Essays Res 2011;5:67-71. doi: 10.4103/0259-1162.84197
20. Fukuta O, Brahom RL, Yanase H, Kurosu K. The sedative effects of intranasal midazolam administration in the dental treatment of patients with mental disabilities. Part 2: optimal concentration of intranasal midazolam. J Clin Pediatr Dent 1994;18:259-65.
21. Miller D, R, Pardo CM. Basics of anesthesia. Elsevier, Mos-bey Saunders, 6th ed;2011. p. 530-5.
22. Gharde P, Chauhan S, Kiran U. Evaluation of efficacy of intra nasal midazolam, ketamin and their mixture as pre-medication and its relation with bispectral index in children with tetralogy of Fallot undergoing intracardiac repair. Ann Card Anaesth 2006;9:25-30.
23. Tsze DS, Steele DW, Machan JT, Akhlaghi F, Linakis JG. Intranasal ketamine for procedural sedation in pediatric lac-eration repair: a preliminary report. Pediatric Emergency Care 2012;28:767-70. doi: 10.1097/pec.0b013e3182624935
24. VahidGolpayegani M, Dehghan F, Ansari G, Shayeghi S. Comparison of oral Midazolam-Ketamine and Midazolam-Promethazine as sedative agents in pediatric dentistry. Dent Res J (Isfahan) 2012;9:36-40. doi: 10.4103/1735-3327.92925
25. Fuks AB, Kaufman E, Ram D, Hovav S, Shapira J. Assess-ment of two doses of intranasal midazolam for sedation of young pediatric dental patients. Pediatric Dent 1994;16:301-5.
26. Diaz JH. Intranasal ketamine preinduction of pediatric outpa-tients. PaediatrAnaesth 1997;7:273-8. doi: 10.1046/j.1460-9592.1997.d01-93.x
27. Mazaheri R, Eshghi A, Bashardoost N, Kavyani N. Assess-ment of intranasal midazolam administration with a dose of 0.5 mg/kg in behavior management of uncooperative chil-dren. J Clin Pediatr Dent 2008;32:95-9. doi: 10.17796/jcpd.32.2.t4v60w22h712uu78
Masoud Fallahinejad Ghajari1 * Ghassem Ansari2 * Ali Asghar Soleymani3* * Shahnaz Shayeghi4 * Faezeh Fotuhi Ardakani5
1Associate Professor & Head, Department of Pediatric Dentistry, School of Dentistry, Shahid Beheshti University of Medical Sciences, Tehran, Iran
2Professor, Research Institute of Dental Sciences, Department of Pediatric Dentistry, School of Dentistry, Shahid Beheshti University of Medical Sciences, Tehran, Iran
3Assistant Professor, Department of Pediatric Dentistry, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran
4Associate Professor, Department of Anesthesiology, Shahid Beheshti University of Medical Sciences, Tehran, Iran
5Assistant Professor, Department of Pediatric Dentistry, School of Dentistry, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
*Corresponding Author; E-mail: [email protected]
Received: 22 January 2014; Accepted: 12 January 2015
J Dent Res Dent Clin Dent Prospect 2015; 9(2):61-65 | doi: 10.15171/joddd.2015.013
This article is available from: http://dentistry.tbzmed.ac.ir/joddd
© 2015 The Authors; Tabriz University of Medical Sciences
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Copyright Tabriz University of Medical Sciences Spring 2015
Abstract
There are several known sedative drugs, with midazolam and ketamine being the most commonly used drugs in children. The aim of this study was to compare the effect of intranasal and oral midazolam plus ketamine in children with high levels of dental anxiety. A crossover double-blind clinical trial was conducted on 23 uncooperative children aged 3-6 (negative or definitely negative by Frankel scale), who required at least two similar dental treatment visits. Cases were randomly given ketamine (10 mg/kg) and midazolam (0.5 mg/kg) through oral or intranasal routes in each visit. Intranasal administration was more effective in reduction of crying and movement during dental procedures compared to oral sedation. Overall behavior control was scored higher in nasal compared to oral routes at the time of LA injection and after 15 minutes. The difference was found to be statistically significant at the start and during treatment. However, the difference was no longer significant after 30 minutes, with the vital signs remaining within physio-logical limits.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer





