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Somatropin (Genotropin) (0.15 mg/day to 0.3 mg/day): Replacement of Endogenous Growth Hormone in Adults with Growth Hormone Deficiency [Internet]. Ottawa (ON): Canadian Agency for Drugs and Technologies in Health; 2014 Jan.

Cover of Somatropin (Genotropin) (0.15 mg/day to 0.3 mg/day)

Somatropin (Genotropin) (0.15 mg/day to 0.3 mg/day): Replacement of Endogenous Growth Hormone in Adults with Growth Hormone Deficiency [Internet].

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2OBJECTIVES AND METHODS

2.1. Objectives

To perform a systematic review of the beneficial and harmful effects of recombinant somatropin (Genotropin) for the treatment of GHD in adults.

2.2. Methods

Studies were selected for inclusion in the systematic review based on the selection criteria presented in Table 1.

Table 1. Inclusion Criteria for the Systematic Review.

Table 1

Inclusion Criteria for the Systematic Review.

The literature search was performed by an information specialist using a peer-reviewed search strategy. Published literature was identified by searching the following bibliographic databases: MEDLINE (1946–) with in-process records and daily updates through Ovid; Embase (1974–) through Ovid; and PubMed. The search strategy consisted of both controlled vocabulary, such as the National Library of Medicine’s MeSH (Medical Subject Headings), and keywords. The main search concepts were Genotropin and Growth Hormone Deficiency.

No filters were applied to limit the retrieval by study type. Retrieval was not limited by publication year or by language. Conference abstracts were excluded from the search results. APPENDIX 2: LITERATURE SEARCH STRATEGY for the detailed search strategies.

The initial search was completed on July 19, 2013. Regular alerts were established to update the search until the meeting of the Canadian Drug Expert Committee (CDEC) on November 20, 2013. Regular search updates were performed on databases that do not provide alert services.

Grey literature (literature that is not commercially published) was identified by searching relevant websites from the following sections of the Grey Matters checklist (http://www.cadth.ca/en/resources/finding-evidence-is/grey-matters), including websites of regulatory agencies, health technology assessment agencies, and clinical guideline repositories. Google and other Internet search engines were used to search for additional web-based materials. These searches were supplemented by reviewing the bibliographies of key papers and through contacts with appropriate experts. In addition, the manufacturer of the drug was contacted for information regarding unpublished studies. APPENDIX 2: LITERATURE SEARCH STRATEGY for more information on the grey literature search strategy.

Two Common Drug Review (CDR) clinical reviewers independently selected studies for inclusion in the review based on titles and abstracts, according to the predetermined protocol. Full-text articles of all citations considered potentially relevant by at least one reviewer were acquired. Reviewers independently made the final selection of studies to be included in the review, and differences were resolved through discussion. No included studies were identified for this report. Excluded studies (with reasons) are presented in APPENDIX 3: EXCLUDED STUDIES.

Copyright © CADTH 2014.

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Except where otherwise noted, this work is distributed under the terms of a Creative Commons Attribution-NonCommercial- NoDerivatives 4.0 International licence (CC BY-NC-ND), a copy of which is available at http://creativecommons.org/licenses/by-nc-nd/4.0/

Bookshelf ID: NBK195547

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