• English

    Google Translate Disclaimer

    The Maryland Department of Information Technology (“DoIT”) offers translations of the content through Google Translate. Because Google Translate is an external website, DoIT does not control the quality or accuracy of translated content. All DoIT content is filtered through Google Translate which may result in unexpected and unpredictable degradation of portions of text, images and the general appearance on translated pages. Google Translate may maintain unique privacy and use policies. These policies are not controlled by DoIT and are not associated with DoIT’s privacy and use policies. After selecting a translation option, users will be notified that they are leaving DoIT’s website. Users should consult the original English content on DoIT’s website if there are any questions about the translated content.

    DoIT uses Google Translate to provide language translations of its content. Google Translate is a free, automated service that relies on data and technology to provide its translations. The Google Translate feature is provided for informational purposes only. Translations cannot be guaranteed as exact or without the inclusion of incorrect or inappropriate language. Google Translate is a third-party service and site users will be leaving DoIT to utilize translated content. As such, DoIT does not guarantee and does not accept responsibility for, the accuracy, reliability, or performance of this service nor the limitations provided by this service, such as the inability to translate specific files like PDFs and graphics (e.g. .jpgs, .gifs, etc.).

    DoIT provides Google Translate as an online tool for its users, but DoIT does not directly endorse the website or imply that it is the only solution available to users. All site visitors may choose to use alternate tools for their translation needs. Any individuals or parties that use DoIT content in translated form, whether by Google Translate or by any other translation services, do so at their own risk. DoIT is not liable for any loss or damages arising out of, or issues related to, the use of or reliance on translated content. DoIT assumes no liability for any site visitor’s activities in connection with use of the Google Translate functionality or content.

    The Google Translate service is a means by which DoIT offers translations of content and is meant solely for the convenience of non-English speaking users of the website. The translated content is provided directly and dynamically by Google; DoIT has no direct control over the translated content as it appears using this tool. Therefore, in all contexts, the English content, as directly provided by DoIT is to be held authoritative.

    Request for Comment on Management of Childhood Lead Exposure
    In May, 2012, the U.S. Centers for Disease Control and Prevention (CDC) responded to recommendations from the Advisory Committee on Childhood Lead Poisoning Prevention (ACCLPP) to revise the guidelines for childhood lead poisoning.  The CDC adopted the ACCLPP’s recommendation that eliminated the term “level of concern” (since there is no known safe blood lead level, or BLL) and the recommendation for a new BLL reference level of 5 mg/dL, based on the current lead levels in the population.  The CDC also agreed in principle with ACCLPP recommendations that “no children in the U.S.[should] live or spend significant time in homes, buildings or other environments with lead-exposure hazards.”  However, CDC did not describe a specific plan to achieve this goal.  The CDC also agreed in principle with the ACCLPP’s recommendations that clinicians should:
    • [B]e a reliable source of information on lead hazards and take the primary role in educating families about preventing lead exposures. This includes recommending environmental assessments PRIOR to blood lead screening of children at risk for lead exposure. 
    • [M]onitor the health status of all children with a confirmed BLL ≥5 μg/dL for subsequent increase or decrease in BLL until all recommended environmental investigations and mitigation strategies are complete, and should notify the family of all affected children of BLL test results in a timely and appropriate manner. 
    • [E]nsure that BLL values at or above the reference value are reported to local and state health and/or housing departments if no mandatory reporting exists and collaborate with these agencies in providing the appropriate services and resources to children and their families.
    CDC also accepted in principle other ACCLPP recommendations regarding the need to emphasize the importance of environmental assessments to identify and mitigate lead hazards before children demonstrate BLLs at or higher than the reference value, and adopt prevention strategies to reduce environmental lead exposures in soil, dust, paint, and water before children are exposed.  However, no specific plans were proposed by CDC for these recommendations. 
    On June 7, 2012, the Department released a letter to health care providers with information about the CDC response and the Department’s position.  Key points of the letter were:
    1. There is no change in the recommendations for the age of testing for children in Maryland.  The requirement remains that children living in zip codes identified as “at-risk”) in the Maryland State Targeting Plan and all children enrolled in Maryland Healthy Kids (EPSDT), should receive a lead test at ages 12 and 24 months.
    2. MDH, consistent with the new CDC guidance, recommends that children with a lead level greater than the new reference level of 5 mg/dL should be retested within 3 months.  In addition, families whose children have a confirmed level greater than 5 mg/dL should receive lead and nutritional education, and be assessed for possible sources of lead exposure.
    3. There has been no change in the Maryland law related to housing and lead levels.  Maryland law still recognizes a level of 10 mg/dL as the level that triggers regulatory action related to rental housing. 
    As noted in the June 7, 2012 letter, children with a venous lead level greater than the new reference level of 5 mg/dL should be retested within 3 months.  A child with a capillary test of 5 – 9 mg/dL should always have a confirmatory venous sample drawn as soon as possible.  In addition, families whose children have a confirmed level greater than 5 mg/dL should receive lead and nutritional education, and be assessed for possible sources of lead exposure.

    Referral and Case Management
    Currently, when the Maryland Childhood Lead Registry (CLR) receives a test of 10 mg/dL or greater, that result is reported to the local health department (LHD) in the jurisdiction where the child resides.
    At that point, there is typically telephone or in-person contact by a case manager at the LHD with the family, to evaluate possible sources of exposure, discuss clinical follow up if necessary, and otherwise manage the case.  This takes place for approximately 500 new cases each year, under the former CDC guidelines. 
    An outstanding question is how the new CDC guidelines should influence current protocols for referral and case management. 
    The Department is considering two alternatives for case management under the new guidelines.  These are:
    1. Continue current case management strategies with lower levels – Under this option, there would be no difference between the LHD response to a child regardless of the lead level – as long as the level is 5 mg/dL or higher, the LHD would do the same thing (contact the family, arrange for follow up if necessary).  Health Departments would be instructed to prioritize children with higher lead levels. Without substantial additional funding, this would likely contribute to a significant increase in workload, and could result in delays in processing cases. 
    2. Create an alternative case management strategy for children with lower blood lead levels – This option involves creation of a modified case management strategy, involving greater reliance on follow up by the primary care provider.  Under this strategy, case managers at the LHD would notify the primary care provider, who would be expected to perform follow-up testing, screen family for risk factors, and refer for case management if indicated. 
    The Department is seeking public comment on the pros and cons of these two strategies and whether other approaches are optimal.  Please comment on whether the current approach to children with lead levels over 10 is optimal for children with leads of 5-9 mg/dL, given potential other sources of lead exposure besides the household for these children.

    Look-Back for Children
    The Department is also requesting comments and public input on the most appropriate management of children who have previously had blood lead levels between 5 – 9 mg/dL.  Prior to the new CDC recommendations, general clinical recommendations were to follow up on children with any detectable lead, since there is no “natural” level of lead in the human body.  However, in practice there may have been children with blood lead levels less than 10 who did not have either a follow up lead test or evaluation to determine whether there was a source of possible lead exposure that could be eliminated.
    The Department is considering working with MDE to notify parents of children who tested between 5 and 9 mg/dL in recent years of the new levels and recommending retesting as an initial step, to be followed up as appropriate.  Possible reasons for retesting might include confirmation of a single capillary test, tests reported to clinicians only as “less than 10,” or other indications. 
    The Department seeks comment on the appropriate length of time for this “look-back,” given the fact that lead exposure peaks by the age of 3 years (36 months) and then starts to decline, particularly after 6 years (72 months) of age.  

    The Department requests comments by Friday, September 28, 2012, on these issues and any other recommendations related to the new CDC guidelines.  The Department has also asked the Lead Poisoning Prevention Commission to review public comments and to make recommendations on whether the Department should take any additional action.  The Lead Poisoning Prevention Commission was created by statute in 1994 (Chapter 114, Acts of 1994).  The Commission studies and collects information on the effectiveness of the Lead Poisoning Prevention Program and current risk reduction treatments in reducing exposure to lead as well as risk and liability issues including availability of insurance (Environment Article, Secs. 6-801, 6-848).  In addition to reviewing written comments, the Council will hold a hearing to solicit public input on the questions above on October 11, 2012.  The Commission will then vote on recommendations to forward to the Secretary of Health and Mental Hygiene regarding the consent form and the consent and age verification procedures.  
    Written comments should be submitted by Friday, September 28, 2012, at 5:00 PM.
    Comments may be submitted by mail to Michele Phinney, Director, Office of Regulation and Policy Coordination, Department of Health and Mental Hygiene, 201 W. Preston St., Room 512, Baltimore, MD 21201 or call 410-767-6499, TTY: 800-735-2258, or by email to mdh.regs@maryland.gov, or by fax to 410-767-6483.