Editors/ Uniform Requirements for Manuscripts Sub-mitted to Biomedical Journals, (http://www.icmje.org Î·È http:// www.icmje.org/icmje.pdf). OÈ Û˘ÓÙÌ‹ÛÂȘ ÙˆÓ Ù›ÙÏˆÓ ÙˆÓ ÂÚÈÔ‰ÈÎÒÓ Á›ÓÔÓÙ·È Ì ‚¿ÛË ÙÔ Cumulated Index Medicus [List of Journals Indexed in Index Medicus (http://www.nlm.nih.gov/bsd/uniform requirements.html)].
Proesmans W. Bartter syndrome and its neonatal variant. Eur J Pediatr 1997;156:669-679.
™˘ÌÏËڈ̷ÙÈÎfi Ù‡¯Ô˜ ÂÚÈÔ‰ÈÎÔ‡:
Flyvbjerg A. Role of growth hormone, insulin-like growth factors (IGFs) and IGF-binding proteins in the renal complications of diabetes. Kidney Int 1997;52 (60 Suppl):S12-S19.
Èڛ˜ Û˘ÁÁڷʤ·:
National Institutes of Health Consensus Development Conference. Neurofibromatosis conference statement. Arch Neurol 1988;45:575-578.
¶ÚÔÛ‰ÈÔÚÈÛÌfi˜ Ù‡Ô˘ ¿ÚıÚÔ˘:
Schreiner GF, Lange L. Ethanol modulation of macrophage influx in glomerulonephritis [Abstract]. J Am Soc Nephrol 1991;2:562.
Should antileukotriene therapies be used instead of inhaled corticosteroids in asthma? [Editorial]. Am J Respir Crit Care Med 1998;158:1697-1701.
Laux-End R, Inaebnit D, Gerber HA, Bianchetti MG. Vasculitis associated with levamisole and circulating autoantibodies [Letter]. Arch Dis Child 1996;75:355-356.
II. µπµ§π∞
∫ÂʿϷÈÔ Û ‚ȂϛÔ:
Clark AG, Barratt TM. Steroid-responsive nephrotic syndrome. In: Barratt TM, Arner ED, Harmon WE, editors. Pediatric Nephrology. 4th ed. Baltimore: Lippincott William Wilkins; 1999. p. 742.
™‡ÁÁÚ·ÌÌ· ‹ ÌÔÓÔÁÚ·Ê›·:
Gorlin RJ, Cohen MM, Levin LS. Syndromes of the head and neck. 3rd ed. New York: Oxford University Press; 1990.
¢ËÌÔÛ›Â˘ÛË Û ÙfiÌÔ Ú·ÎÙÈÎÒÓ: Bauer AW. The two definitions of bacterial resistance. In: Smith AJ, Rogers CA, eds. Proceedings of the Third International Congress of Chemotherapy; 1962 May 29-31; New York: International Society of Chemotherapy; 1963. p. 484-500.
Kaplan SJ. Post hospital home health care: the elderly’s access and utilization [dissertation]. St. Louis (Mo): Washington Univ.; 1995.
πππ. CD-ROM
Anderson SC, Poulsen KB. Anderson’s electronic atlas of hematology [CD-ROM]. Philadelphia: Lippincott Williams & Wilkins; 2002.
IV.™∆O ¢π∞¢π∫∆ÀO ÕÚıÚÔ Û ÂÚÈÔ‰ÈÎfi:
Abood S. Quality improvement initiative in nursing homes: the ANA acts in an advisory role. Am J Nurs [Internet]. 2002 Jun: Webpage: http://www.nursingworld.org/AJN/2002/june/Wawatch.htm
ªÔÓÔÁÚ·Ê›·:
Foley KM, Gelband H, editors. Improving palliative care for cancer [Monograph, Internet]. Washington: National Academy Press; 2001. Webpage: http://www.nap.edu/books/0309074029/html
πÛÙÔÛÂÏ›‰Â˜:
Cancer-Pain.org [Webpage, Internet]. New York: Association of Cancer Online Resources, Inc.; 2002: http://www.cancer-pain.org/
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The Greek Paediatric Society is the owner of “Paediatriki”, its official scientific journal, which is distributed to its members. Its objectives are the publication of paediatric scientific work and the continuing education of paediatricians. For this purpose, it publishes a variety of articles, and in particular:
1.Editorials (upon invitation by the Editorial Board).
2.Review articles.
3.Award-winning articles.
4.Original articles.
5.Clinical Quiz.
6.Round tables.
7.Current issues.
8.Issues of healthcare management and education.
9.Case reports.
10.News.
11.Brief reports.
12.Letters to the editor.
13.Abstracts.
14.Future congresses and events.
15.Book reviews.
The Editorial Board reserves the right to publish articles of special scientific interest and articles on current issues without observing submission order. In addition it publishes upon decision original papers presented at the Annual Paediatric Conference, presentations of special interest - in whole or in part, and letters - in whole or in part - referring to scientific articles published in the journal.
Regarding papers on current issues, the author’s request for immediate publication should be quoted on the first page. The Editorial Board reserves the right to accept such papers for immediate publication.
All manuscripts should not have been published previously, in whole or in part, and not be under consideration by another publication. Manuscripts should acknowledge any funding, sponsorship or other financial support. All clinical research should have been conducted following informed consent of participants or of their legal representatives according to the Declarations of Helsinki and Tokyo. In addition, the US National Institute of Health guide for the care and use of laboratory animals (DHEW Publication, NIH, 80-23) should have been observed. Clinical trials should have been approved by the Ethics Committee of the Hospital.
Authors’ opinions and conclusions expressed in the published papers do not necessarily reflect those of the journal. The Greek Paediatric Society, the Editorial Board and the Publisher of the journal do not necessarily approve the content of the advertisements appearing in the journal.
The copyright of all published papers is held by “Paediatriki” and their reproduction in whole or in part is authorized only following written consent of the journal.
B. Manuscript Preparation
“Paediatriki” suggests compliance with the “Uniform Requirements for Manuscripts Submitted to Biomedical Journals”, recently modified and published on the websites:
http://www.icmje.org and http://www.icmje.org/icmje.pdf
The entire paper (including figure legends and tables)
should be typed on one side of blank paper format A4 (21x29.7 cm), double line spacing and minimum indent 2.5 cm on both sides.
The paper should have the following structure: title page, short title, abstract in Greek and English, list of abbreviations, text, acknowledgements and quoting of grants, sponsorships or other financial support sources, references, tables, figures, figure legends. Each of these sections should be started on a new page. Pages should be numbered consecutively, beginning with the title page.
Text length shall be:
ñ review articles 2000-3000 words;
ñ original articles 1500-2500 words and case reports 1000-1500 words;
ñ the title (<14 words) and the short title (<5 words) of the article. No abbreviations are permitted in the title;
ñ the name and surname of all authors;
ñ the centre (institution, clinic, laboratory) of origin of the paper. If there is no affiliation with a specific centre, the status of the author(s) should be cited (e.g., private paediatrician) and home address;
ñ the complete address, e-mail and telephone number of the author to whom correspondence should be addressed.
Abstracts
The abstract should summarize the objectives, methodology, main results and conclusions of the study.
ñ It should contain at least 200 words, and not exceed 250 words.
ñ It should consist of the following paragraphs: background, methods, results and conclusions.
The English abstract should cite at the beginning the title of the paper and the authors’ names in English. The content of the text should consist of the following paragraphs: background, methods, results and conclusions. The abstract in English should not differ in content from the corresponding Greek abstract.
Beneath the Greek and English abstracts, three to five key words in the respective language should be supplied, to be used in the thematic index.
Text
Original articles include: introduction, methods, results and discussion. The introduction includes the latest research data on the subject and the main references and the objectives of the paper. The description of the methods should be precise and detailed so as to enable reproduction by other researchers. In addition, the statistical methods of analysis and evaluation of the results should be described. Results should be presented clearly, together with the appropriate statistical analysis. Discussion should cover the results ensuing from the research, their significance and possible associations with the observations of other researchers.
Case reports comprise a short introduction, case description and brief discussion, with emphasis on differential diagnosis.
The structure of all other articles is free, according to the judgment of the authors.
Thanks or acknowledgements (reference to grants, sponsorships or other sources of financial support) should be quoted at the end of the text, before references.
Units of measures of laboratory analyses
Laboratory analyses should be expressed in the Système International (SI) units and in the metric (Conventional) system in parentheses. See conversion tables on the websites: http://www.icmje.org and http://www.icmje.org/icmje.pdf
Abbreviations
All issues of the journal contain internationally established abbreviations. Complex or long terms often repeated in the text may be replaced by abbreviations explained by the authors in a list submitted with the paper. Abbreviations are reported in parentheses only in abstracts.
References
The reference section contains all references numbered in the order in which they appear in the text. In the text, references are to be indicated by Arabic numerals in parentheses. References should be no more than:
ñ 70 in review articles;
ñ 30 in original articles;
ñ 12 in current issues and case reports;
ñ5 in brief reports and letters.
In listing references follow the recently modified standards of the International Committee of Medical Journal Editors/Uniform Requirements for Manuscripts Submitted to Biomedical Journals, (http://www.icmje.org and http:// www.icmje.org/icmje.pdf). Abbreviated names of journals should conform to the Cumulated Index Medicus [List of Journals Indexed in Index Medicus (http://www.nlm.nih.gov/bsd/uniform requirements.html)].
Examples of reference style
I. JOURNALS
All authors are cited if they are six or less; if they are 7 or more, the first six are cited, followed by “et al”.
Regular edition:
Proesmans W. Bartter syndrome and its neonatal variant. Eur J Pediatr 1997;156:669-679.
Supplement issue:
Flyvbjerg A. Role of growth hormone, insulin-like growth factors (IGFs) and IGF-binding proteins in the renal complications of diabetes. Kidney Int 1997;52 (60 Suppl):S12-S19.
No author:
National Institutes of Health Consensus Development Conference. Neurofibromatosis conference statement. Arch Neurol 1988;45:575-578.
Article type specification:
Schreiner GF, Lange L. Ethanol modulation of macrophage influx in glomerulonephritis [Abstract]. J Am Soc Nephrol 1991;2:562.
Should antileukotriene therapies be used instead of inhaled corticosteroids in asthma? [Editorial]. Am J Respir Crit Care Med 1998;158:1697-1701.
Laux-End R, Inaebnit D, Gerber HA, Bianchetti MG. Vasculitis associated with levamisole and circulating autoantibodies [Letter]. Arch Dis Child 1996;75:355-356.
II. BOOKS
Chapter in book: Clark AG, Barratt TM. Steroid-responsive nephrotic syndrome. In: Barratt TM, Arner ED, Harmon WE, editors. Pediatric Nephrology. 4th ed. Baltimore: Lippincott William Wilkins; 1999. p. 742.
Book or monograph:
Gorlin RJ, Cohen MM, Levin LS. Syndromes of the head and neck. 3rd ed. New York: Oxford University Press; 1990.
Publication in a volume of proceedings:
Bauer AW. The two definitions of bacterial resistance. In: Smith AJ, Rogers CA, eds. Proceedings of the Third International Congress of Chemotherapy; 1962 May 29-31; New York: International Society of Chemotherapy; 1963. p. 484-500.
Doctoral dissertation:
Kaplan SJ. Post hospital home health care: the elderly’s access and utilization [dissertation]. St. Louis (Mo): Washington Univ.; 1995.
πππ. CD-ROM
Anderson SC, Poulsen KB. Anderson’s electronic atlas of hematology [CD-ROM]. Philadelphia: Lippincott Williams & Wilkins; 2002.
IV. ON THE INTERNET
Article in journal
Abood S. Quality improvement initiative in nursing homes: the ANA acts in an advisory role. Am J Nurs [Internet]. 2002 Jun: Webpage: http://www.nursingworld.org/ AJN/2002/june/Wawatch.htm
Monograph
Foley KM, Gelband H, editors. Improving palliative care for cancer [Monograph, Internet]. Washington: National Academy Press; 2001. Webpage: http://www.nap.edu/books/0309074029/html
Websites
Cancer-Pain.org [Webpage, Internet]. New York: Association of Cancer Online Resources, Inc.; 2002: http://www.cancer-pain.org/
Tables and Figures
Three copies should be submitted (original plus 2 copies). Their width should either be equal to the width of one column (7.5 cm) or to the width of the page (15.5 cm). Their maximum length, titles included, should not exceed 22 cm.
Tables are numbered with Arabic numerals in the order in which they appear in the text. They should have a short title and abbreviations should be listed at the bottom. Vertical lines in tables should be avoided.
All illustration material is considered as figures (graphs, pictures, etc.). They should be of excellent quality. Also, at the back of every picture, the number of the picture and the name of the first author should be noted in pencil, with an arrow showing the top of the picture. The identity of patients should not be recognizable from their pictures nor should their names be stated.
C. Manuscript Submission and Publication
All manuscripts should be accompanied by a floppy disk or CD, as well as by a letter, signed by all the authors, in which it is stated that the paper has not been published in part or in whole, or is not under consideration by another journal and that the authors accept its publication in “Paediatriki”. Any funding, sponsorship or other financial support should be acknowledged.
Once the manuscript has been accepted, the corrected version, rewritten according to the reviewers’ recommendations should be submitted to the Editorial Board accompanied by a floppy disk or CD, containing the paper in Word format, along with a covering letter specifying in detail the modifications or objections to the reviewers’ suggestions.
Delay in submission of the modified paper exceeding 30 days entails new submission.
Authors will be charged film and reprint expenses, paid upon dispatch of the first proof directly to the printer.
Manuscripts of papers which have not been approved for publication are not returned to the author. The accompanying figures and photographs can be returned upon request within six months.
Manuscripts submitted for review and publication in “Paediatriki” should be sent in three copies to the following address: Editorial Board, Greek Paediatric Society 92, Michalakopoulou Street, 115 28 Athens, Greece
Before submitting your paper, make sure it contains:
1.3 copies of the text of the paper, printed according to instructions.
2.A floppy disk or CD with the entire material of the paper (text, tables, pictures).
3.A covering letter and a statement that the paper has not been previously published.
4.The title page (on a separate page), which includes: a.the title and short title of the paper; b.the name and surname (full name)of the author(s); c.the academic centre(s) of origin; d.the corresponding authors’ name, address and telephone number;
5.English and Greek abstracts, with the following structure: background, methods, results and conclusions (double space, separate page) and keywords.
6.List of abbreviations (double space, separate page).
7.Text (double space, separate page).
8.Acknowledgements and reference to funding, sponsorships or other financial sources.
9.References (double space, separate page).
10.Tables (one per page) in three copies.
11.Figures with an arrow at the back showing the top, numbered, in two copies.
12.Figure titles (double space - on separate pages) in three copies.
Diphtheria, tetanus and acellular pertussis booster vaccination for adolescents: ∆he new data
G. Tsolas
Abstract: The number of cases of pertussis continue to increase in the US and other developed countries, despite high immunization coverage rates of infants and young children. As immunity from the primary childhood immunization series wanes, adolescents and adults become susceptible to infection. A large part of the reported increase is thought to be due to increasing physician recognition of pertussis as a cause of nonspecific, persistent cough in adolescents and adults. The spread of infection by adolescents and adults may also place more vulnerable patients, including babies and young infants, at greater risk. In summer 2005, the US Food and Drug Administration (FDA) approved two new combination tetanus, diphtheria, and acellular pertussis (Tdap) vaccines for booster immunization beyond the primary childhood immunization series. These products are intended to replace the current tetanus-diphtheria (Td) booster given at 11-12 years of age. This new Tdap product provides significant increases in pertussis antibody titers and appears to be well tolerated. It has the potential to provide considerable benefit, both in reducing the frequency of pertussis in adolescents and adults and in minimizing the spread of infection to younger high-risk patient populations.
1.Centers for Disease Control and Prevention. Notifiable diseases/ deaths in selected cities weekly information. MMWR Morb Mortal Wkly Rep 2004;53: 1213-1221.
2.Centers for Disease Control and Prevention. Pertussis United States 1997-2000. MMWR Morb Mortal Wkly Rep 2002;51:73-76.
3.Guris D, Strebel PM, Bardenheier B, Brennan M, Tachdjian R, Finch E et al. Changing epidemiology of pertussis in the United States: increasing reported incidence among adolescents and adults, 19901996. Clin Infect Dis 1999;28:1230-1237.
4.Centers for Disease Control and Prevention. Final: 2003 reports of notifiable diseases. MMWR Morb Mortal Wkly Rep 2004;53:687-696.
5.Tanaka M, Vitek CR, Pascual FB, Bisgard KM, Tate JE, Murphy TV. Trends in pertussis among infants in the United States, 1980-1999. JAMA 2003;290: 2968-2975.
6.Celentano LP, Massari M, Paramatti D, Salmaso S, Tozzi AE; EUVAC-NET Group. Resurgence of pertussis in Europe. Pediatr Infect Dis J 2005;24(9): 761-765.
7.Rothstein E, Edwards K. Health burden of pertussis in adolescents and adults. Pediatr Infect Dis J 2005; 24 (5 Suppl):S44-S47
8.Davis JP. Clinical and economic effects of pertussis outbreaks. Pediatr Infect Dis J 2005;24 (6 Suppl): S109-S116.
9.Lee GM, Lett S, Schauer S, LeBaron C, Murphy TV, Rusinak D et al; Massachusetts Pertussis Study Group. Societal costs and morbidity of pertussis in adolescents and adults. Clin Infect Dis 2004;39: 1572-1580.
10.De Serres G, Shadmani R, Duval B, Boulianne N, Dery P, Douville Fradet M et al. Morbidity of pertussis in adolescents and adults. J Infect Dis 2000;182:174-179.
11.Schellekens J, von Konig CH, Gardner P. Pertussis sources of infection and routes of transmission in the vaccination era. Pediatr Infect Dis J 2005;24 (5 Suppl):S19-S24.
12.Bisgard KM, Pascual FB, Ehresmann KR, Miller CA, Cianfrini C, Jennings CE et al. Infant pertussis: who was the source? Pediatr Infect Dis J 2004;23:985-989.
13.Pichichero ME, Casey JR. Acellular pertussis vaccines for adolescents. Pediatr Infect Dis J 2005;24 (6 Suppl):S117-S126.
15. Boostrix prescribing information. GlaxoSmith Kline, May 2005.
16.Adacel prescribing information. Sanofi Pasteur, June 2005.
17.Van Damme P, Burgess M. Immunogenicity of a combined diphtheria-tetanus-acellular pertussis vaccine in adults. Vaccine 2004;22:305-308.
18.Pichichero ME, Rennels MB, Edwards KM, Blatter MM, Marshall GS, Bologa M et al. Combined tetanus-diphtheria, and 5-component pertussis vaccine for use in adolescents and adults. JAMA 2005;293:3003-3011.
19.Southern J, Andrews N, Burrage M, Miller E. Immunogenicity and reactogenicity of combined acellular pertussis/ tetanus/ low dose diphtheria vaccines given as a booster to UK teenagers. Vaccine 2005;23:3829-3835.
20.Humiston SG, Rosenthal SL. Challenges to vaccinating adolescents: vaccine implementation issues. Pediatr Infect Dis J 2005;24 (6 Suppl):S134-S140.
21.Hay JW, Ward JI. Economic considerations for pertussis vaccination in adolescents. Pediatr Infect Dis J 2005;24 (6 Suppl):S127-S133.
22.Purdy KW, Hay JW, Botteman MF, et al. Evaluation of strategies for use of acellular pertussis vaccine in adolescents and adults: a cost-benefit analysis. Clin Infect Dis 2004;39:20-28.
23.Iskedjian M, Walker JH, Hemels ME. Economic evaluation of an extended acellular pertussis vaccine programme for adolescents in Ontario, Canada. Vaccine 2004;22:4215-4227.
24.Caro JJ, Getsios D, El-Hadi W, Payne K, O'Brien JA. Pertussis immunization of adolescents in the United States:an economic evaluation. Pediatr Infect Dis J 2005;24:S75-S82.
25.Lee GM, Lebaron C, Murphy TV, Lett S, Schauer S, Lieu TA. Pertussis in adolescents and adults: should we vaccinate? Pediatrics 2005;15:1675-1684.
26.Campins-Marti M, Cheng HK, Forsyth K, Guiso N, Halperin S, Huang LM et al; International Consensus Group on Pertussis Immunisation. Recommendations are needed for adolescent and adult pertussis immunization; rationale and strategies for consideration. Vaccine 2001;20:641-646.
27. 27. Plotkin S. The global pertussis initiative: process overview. Pediatr Infect Dis J 2005;24 (5 Suppl):S7-S9.
Polio control after certification: evaluating the risks and planning public health policies
K. Douros, B. Tsagris, P. Nikolaidou – Karpathiou
Abstract: Since the 1988 World Health Assembly resolution to eradicate poliomyelitis, considerable progress has been made towards interrupting the transmission of wild poliovirus globally. As the achievement and certification of polio eradication draws near, WHO is evaluating potential postcertification policies. Since the year 2000, it has been realized that the risks of paralytic poliomyelitis in the post-certification era fall into two general categories: those due to the continued use of the oral poliovirus vaccine (OPV) and those due to future improper handling of wild polioviruses. The specific risks within each category have now been defined and further research is under way in order to be quantified properly. The knowledge of nature and magnitude of these risks is of outmost importance in constructing a framework for the evolution of public health policies for the post certification era. However, this framework must be regarded as a dynamic tool, requiring regular updating as additional information on these risks becomes available. There are four broad (and interrelated) areas for which policies must be designed: detection and notification of circulating polioviruses, biocontainment, vaccine stockpiles and response mechanisms, and routine immunization against polioviruses. The process of final decisions is expected to begin at the near future.
Key words: Poliomyelitis, eradication, public health.
1.World Health Assembly. Global eradication of poliomyelitis by the year 2000. Geneva: World Health Organization; 1988 [Resolution 41.28].
2.World Health Organization. Progress towards global eradication of Poliomyelitis 2003 and JanuaryApril 2004. Wkly Epidemiol Rec 2004;79:229-234.
3.World Health Organization. Report by the Secretariat: Eradication of Poliomyelitis. Executive Board, 117 Session, Provisional agenda item 4.4. Geneva, 8 December 2005.
4.Heymann DL. Polio eradication: finishing the job
and protecting the investment. Bull World Health Organ 2004 Jan;82:1.
5. Smith J, Leke R, Adams A, Tangermann RH. Certification of polio eradication: process and lessons learned. Bull World Health Organ. 2004 Jan;82:24-30.
6.Minor PD, Dunn G. The effect of sequences in the 5' non-coding region on the replication of polioviruses in the human gut. J Gen Virol 1988;69:1091-1096.
7.Andrus JK, Strebel PM, de Quadros CA, Olive JM. Risk of vaccine-associated paralytic poliomyelitis in Latin America, 1989-91. Bull World Health Organ 1995;73:33-40.
8.Report of the interim meeting of the Technical Consultation Group (TCG) on the global eradication of poliomyelitis, Geneva, 13-14 Nov 2002. Geneva: World Health Organization; 2003. WHO document WHO/EPI/GEN/02.
9.Kew MK, Wright PF, Agol VA, Delpeyroux F, Shimizu H, Nathanson N, et al. Circulating vaccine-derived polioviruses: current state of knowledge. Bull World Health Organ 2004;82:16-23.
10.Kew O, Morris-Glasgow V, Landaverde M, Burns C, Shaw J, Garib Z, et al. Outbreak of poliomyelitis in Hispaniola associated with circulating type 1 vaccine-derived poliovirus. Science 2002;296:356-359.
12.Paralytic poliomyelitis in Madagascar, 2002. Wkly Epidemiol Rec 2002;77:241-242.
13.Centers for Disease Control and Prevention. Circulation of a type 2 vaccine-derived poliovirusEgypt, 1982-1993. MMWR Morb Mortal Wkly Rep 2001;50:41-42, 51.
14.Halsey NA, Pinto J, Espinosa-Rosales F, Faure-Fontenla MA, da Silva E, Khan AJ, et al; Polio Project Team. Search for poliovirus carriers among people with primary immune deficiency diseases in the United States, Mexico, Brazil, and the United Kingdom. Bull World Health Organ 2004;82:3-8.
15.Dowdle WR, Wolff C, Sanders R, Lambert S, Best M. Will containment of wild poliovirus in laboratories and inactivated poliovirus vaccine production sites be effective for global certification? Bull World Health Organ. 2004;82:59-62.
16. World Health Organization. Poliovirus type 2 (MEF-1) found in northern India. Polio Lab Network Quarterly Update 2003;9:1-2.
17. WHO global action plan for laboratory containment of wild polioviruses. Geneva: World Health Organization; 1999. WHO document WHO/V&B/99.32.
18.World Health Organization. Completion of a national laboratory inventory for global wild poliovirus containment, United States. Wkly Epidemiol Rec. 2003;79: 213-220.
19.Aylward RB, Cochi SL. Framework for evaluating the risks of paralytic poliomyelitis after global interruption of wild poliovirus transmission. Bull World Health Organ. 2004;82:40-46.
20.World Health Organization. Progress towards global eradication of poliomyelitis, 2003 and January-April 2004. Wkly Epidemiol Rec 2004;79:229-234.
21.Hardiman M. The revised International Health Regulations: a framework for global health security. Int J Antimicrob Agents. 2003;21:207-211.
22.World Health Assembly. Poliomyelitis eradication. Geneva: World Health Organization; 1999 [Resolution 52.22].
23.Dowdle WR. The principles of disease elimination and eradication. In: Global disease elimination and eradication as public health strategies. Proceeding of a conference held in Atlanta, Georgia, USA, 23-25 February 1998. Bull World Health Organ 1998;76 (Suppl 2):22 5.
24.Sutter RW, Càceres VM, Lago P. The role of routine
polio immunization in the post-certification era. Bull World Health Organ 2004;82:31-39.
25.Global eradication of poliomyelitis. Report of the meeting on the scientific basis for stopping polio immunization, Geneva, 23-25 March 1998, WHO/ EPI/GEN/98.12.
26.Report of the seventh meeting of the Technical Consultative Group (TCG) on the global eradication of poliomyelitis, Geneva, 2002. Geneva: World Health Organization; 2002.
27.Fine PE, Oblapenko G, Sutter RW. Polio control after certification: major issues outstanding. Bull World Health Organ 2004;82:47-52.
The PANDAS hypothesis (paediatric autoimmune neuropsychiatric disorders associated with streptococcal infection): reality or myth?
V. Tsagris, ∫. Douros, P. Nikolaidou - Karpathiou
Abstract: Various inflammatory disorders have been shown to be associated with preceding streptococcal infections, including acute rheumatic fever, post-streptococcal reactive arthritis, erythema nodosum and post-streptococcal glomerulonephritis. The spectrum of post-streptococcal disease has been expanded with the addition of the paediatric autoimmune neuropsychiatric disorders associated with streptococcal infection (PANDAS). PANDAS are a recently described subgroup of childhood disorders, and there has been a great deal of public and physician interest in their pathophysiology, diagnosis and management. The likelihood that neuropsychiatric disorders such as obsessive-compulsive disorder (OCD) and tics are related to a preceding streptococcal infection is certainly controversial. The current literature is reviewed, culminating in the conclusion that PANDAS remains a yet-unproven assumption.
1.Kiessling LS. Tic disorders associated with evidence of invasive group A beta hemolytic streptococcal disease. Dev Med Child Neurol 1989;31 (Suppl 59):S48.
2.Swedo SE, Leonard HL, Garvey M, Mittleman B, Allen AJ, Perlmutter S et al. Pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections: clinical description of the first 50 cases. Am J Psychiatry 1998;155:264-271.
4.Husby G, van de Rijn I, Zabriskie JB, Abdin ZH, Williams RC Jr. Antibodies reacting with cytoplasm of subthalamic and caudate nuclei neurons in chorea and acute rheumatic fever. J Exp Med 1976;144:1094-1110.
5.Murphy ML, Pichichero ME. Prospective identification and treatment of children with pediatric autoimmune neuropsychiatric disorder associated with group A streptococcal infection (PANDAS). Arch Pediatr Adolesc Med 2002;156:356-361.
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Congenital and acquired heart diseases. Implications for pregnancy, the fetus and the newborn infant
S. Antoniadis
Abstract: Improvements in the diagnosis, intervention and surgical management of congenital heart disease (CHD) during recent years have led in increasing numbers of women with heart problems reaching childbearing age. In the majority of cases, pregnancy in women with cardiovascular does not cause serious problems to the mother or fetus, but there are cases in which maternity should be discouraged or prohibited.
The major problems for the fetus are fetal loss, prematurity, low birth weight and a variety of other problems such as haemorrhage, teratogenesis, etc. Apart from the increased mortality, pregnancy in a woman with cardiovascular disease may cause significant changes in the haemodynamics of the maternal circulation (heart failure, arrhythmia etc.) with need for intensive care by expert doctors and hospital staff.
For the optimal management in such cases, early counselling of the patient and those in her environment about the possible problems is very important. It is essential to know the history, to have a recent evaluation of the maternal cardiac functional status before pregnancy and to take appropriate medical or interventional treatment measures. The maternal life expectancy and the recurrence risk should be considered as factors of major importance. Normal vaginal delivery with forceps assistance is
the birthing choice, except for cases with Marfan syndrome, the possibility of aortic aneurysm or coagulation problems in patients with artificial valves, when caesarian section is preferred.
A high level of knowledge of the problems that pregnancy may cause to mothers with cardiovascular disease will certainly minimize the possible dangers of pregnancy to acceptable levels.
Key words: Congenital and acquired heart diseases, pregnancy.
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Professor of Clinical Psychology University of Athens, Faculty of Nursing 123 Papadiamantopoulou St., 11527, Athens
E-mail: dpap@cc.uoa.gr
Date of submission: 21-09-2004
Date of approval: 22-07-2005
Paediatric palliative care: perceptions of Greek pediatricians
M.
Bouri, D. Papadatou
Abstract: Paediatric palliative care, aimed at the provision of physical, psychosocial and spiritual care for children living with life-limiting diseases and their families, is recognised as an evolving field of paediatrics. In Greece, specialized palliative care services have not yet been developed, although certain elements of such care are being provided in oncology and intensive care settings. The aims of this descriptive study were: a) to investigate the extent of knowledge about paediatric palliative care of Greek paediatricians working in the above settings, and b) to determine their perceptions with regard to the effectiveness of provision of palliative care services in their respective units. The findings revealed that the philosophy and principles of paediatric palliative care have not been fully comprehended by Greek paediatricians, leading to inadequate and inefficient application of palliative care in clinical practice. Their approach remains mainly medically centred, focusing on pain management and symptom control. According to their perceptions, psychosocial and spiritual support is inadequately offered to children and families in their work settings. The participants recognised their lack of knowledge as the major barrier to the application of palliative care. They identified the need for education and training for the effective provision of palliative care and for the staffing of their units with specialized medical, nursing staff and mental health professionals. In conclusion, education in paediatric palliative care is an essential prerequisite for the development of palliative care programmes for terminally ill children and their families in Greece.
Key words: Palliative care, terminal care, death, childhood.
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Food advertisements targeted at children: nutritional information and appeals
E. Bathrellou, M. Yannakoulia, N. Voutzourakis, P. Zisis, A.L. Matalas, L.S. Sidossis
Abstract
Background: The aim of the present study was to perform a content and appeal techniques’ analysis of the television food advertisements targeted at children.
Methods: Nine hundred sixty eight advertisements were recorded during 51 hours of children’s program on 2 consecutive weekends. Data on the type of the advertisement, the food category and appeals in the format and the scenario of the advertisements were collected.
Results: More than half (53.7%) of all advertisements were about food. Food advertisements were more likely than non-food advertisements to use techniques, which make them appealing to kids, such as more shots per ad (13.1±6.6 vs. 12±7.65, p=0.018), faster pace (0.67± 0.28 shots/sec vs. 0.64± 0.29 shots/sec, p=0.10), use of cartoon characters (66.7% vs. 13.2%, ¯2=232.5, p<0.001) and scenario inspired from children’s every day life. The most popular appeal method for food advertisements was promotion of the physical properties of the product (68.3%), followed by appeals for mood alteration (46.9%) and premium offers (40.6%). Analysis of the food categories advertised showed that almost one
10-02-2006
Laboratory of Nutrition and Clinical Dietetics, Department of Nutrition and Dietetics, Harokopio University, Athens, Greece
Correspondence: Labros S. Sidossis Laboratory of Nutrition and Clinical Dietetics, Department of Nutrition and Dietetics, Harokopio University 70, El. Venizelou Str. 176 71 Athens, Greece E-mail: lsidossis@hua.gr
Date of submission: 01-04-2005
Date of approval: 10-02-2006
third (31.7%) of the food advertisements were for dairy products. Other most advertised food categories were confectionary snacks (21%) and chocolate products (11.5%). Nutritional value analysis revealed that the majority of the foods advertised were high in sugar and fat.
Conclusions: The present study sets the framework for further thinking and research concerning the relationship of food advertisements and dietary habits in children.
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Abstract: In 1987 Casamassima and colleagues described a new syndrome, with an appearance resembling the Smith-Lemli-Opitz syndrome (SLOs) and the Meckel syndrome (Ms), associated with the presence of cerebellar deficit. The case is described of a male infant which matches the clinical appearance of this syndrome. The infant had hypoplasia of the cerebellar vermis and phenotype of the SLOs type II, but without the biochemical abnormalities of SLOs.
ÓÂÔÁÓÔ‡. √ ÔÛÔÙÈÎfi˜ ÚÔÛ‰ÈÔÚÈÛÌfi˜ ÙˆÓ ÙÈÌÒÓ Ù˘ 7-‰Â¸‰ÚÔ-¯ÔÏËÛÙÂÚfiÏ˘, ‰ÂÛÌÔÛÙÂÚfiÏ˘, Ï·ıÔÛÙÂÚfiÏ˘, ¯ÔÏÂÛÙ·ÓfiÏ˘, Ï·ÓÔÛÙÂÚfiÏ˘, 8(9)-¯ÔÏÂÛÙÂÓfiÏ˘ Î·È Ù˘ 8-‰Â¸‰ÚÔ¯ÔÏËÛÙÂÚfiÏ˘ ÙÔ˘ ·›Ì·ÙÔ˜, ¤ÁÈÓ ÛÙÔ Institute of Child Health and Great Ormond Street Hospital for Children, University College London
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1st Paediatric Clinic, Aristotle University, “Ippokration” General Hospital, Thessaloniki
Correspondence: H. Hatzissevastou-Loukidou Laboratory of Cytogenetics 1st Paediatric Clinic, Aristotle University, “Ippokration” General Hospital, Thessaloniki 49 Konstantinoupoleos Str., 546 42, Thessaloniki
Date of submission: 17-12-2004
Date of approval: 22-07-2005
Lethal multiple pterygium syndrome
H. Hatzissevastou - Loukidou, ∞. Georgountzou
Abstract: Lethal multiple pterygium syndrome (LMPS) is characterized by hydrops fetalis, and intrauterine death, where the fetus has multiple pterygia or wing-like webs of skin across joints, which are always associated with joint contractures. The inheritance is either autosomal or X-linked recessive. In high risk pregnancies prenatal diagnosis is possible by ultrasound examination at 14 to 16 weeks’ gestation, which relies on identification of the characteristic fetal anatomical abnormalities and their evolution. A family is reported whose first male child was affected with fatal LMPS. Genetic counselling was provided to his parents, his parents’ siblings and recently to his adolescent siblings.
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Familial Moyamoya disease in two European children
H.
Bazigou - Fotopoulou1, N. Vassilaki1, S. Aroni2, H. Ikeda3, A. Papavassiliou1
Abstract: Moyamoya disease (MMD) is characterised by stenosis or occlusion of the main cerebral arteries detected on cerebral angiography. Although the aetiology is still unknown, there is extensive evidence that MMD may follow a multifactorial pattern of inheritance. Two cases are presented of familial MMD in children of European descent, in order to emphasize the occurrence of this rare disease in not only Oriental but also other races, and to stress the hereditary factors in its pathogenesis. The first patient, a Greek girl, has additional coagulation disorders. Her mother, who also suffers from MMD, and various other members of her family, have similar coagulation disorders. The second patient, a Scottish boy, represents a unique case of familial MMD, as five members of three consecutive generations of his maternal family also suffer from MMD.
3 Kohnan Hospital, Department of Neurosurgery, Sendai Japan
AÏÏËÏÔÁÚ·Ê›·:
E-mail: fotopoul@hol.gr
˘Ô‚ÔÏ‹˜: 03-12-2004
21-10-2005
1 Neurology Clinic, General Children’s Hospital of Penteli 2 Department of Haemorragic Dispositions, “Aghia Sofia” Children’s Hospital 3 Kohnan Hospital, Department of Neurosurgery, Sendai Japan
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Abstract: Haemoptysis is rare during childhood. In its management it is first important to distinguish between haemoptysis and haematemesis or epistaxis. Haemoptysis may indicate the presence of severe disease, which could be fatal if not treated appropriately. ∞cute lower respiratory tract infection is the most common cause. Other common causes are cystic fibrosis, localised airway lesions and heart disease. More rare causes include idiopathic pulmonary haemosiderosis and the pulmonary-renal syndromes, which include systemic lupus erythematosus, Goodpasture’s syndrome, Wegener’s granulomatosis, microscopic polyangiitis and Henoch-Schonlein purpura. A plain chest radiograph is mandatory, although one third of children with haemoptysis have a normal chest radiograph. Thorax computed tomography and bronchoalveolar lavage are of great assistance in the investigation. In the majority of children the haemoptysis resolves spontaneously, without the need for invasive measures. The treatment of the child with haemoptysis depends on the underlying aetiology and on the extent of the bleeding. Bronchoscopy with a rigid bronchoscope, embolization of the suspected vessel and surgical resection of the affected lung segment might be required in case of massive bleeding.
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Katz ª, Rubino ∞, Collier J, Rosen J, Ehrich JHH, Demography of Pediatric Primary Care in Europe: Delivery of Care and Training. Pediatrics 2002;109:788-796. http://pediatrics.aappublications.org/cgi/content/full/109/5/788
Academy of Allergology and Clinical Immunology, EAACI)
Teach-In/Medical Update - Paediatrics Edinburgh, ¶ÏËÚÔÊÔڛ˜: The Royal College of Physicians Scotland, UK of Edinburgh, 9 Queen Street, Edinburgh EH2 1JQ
Christina Pottinger
∆ËÏ.: 44 0 1 312 257 324
Fax: 44 0 1 312 203 939
E-mail: c.pottinger@rcpe.ac.uk
24-27 ª·˝Ô˘ 2006
41st Annual Meeting of the Association for Basel, European Paediatric Cardiology (AEPC) Switzerland
¶ÏËÚÔÊÔڛ˜: Dr. Ingrid Oberhänsli-Weiss Ph.D, AEPC Secretary-general,
31 Route de Florissant, CH-1206 Geneva Switzerland