Supporting Statement for Collection of Information
Follow-up Activities for Product-Related Injuries
A. Justification
1. Information to be collected and circumstances that make the collection of
information necessary
Section 5(a) of the Consumer Product Safety Act (CPSA)(15 U.S.C. § 2054(a)) requires the Commission to collect information related to the cause and prevention of death, injury and illness associated with consumer products. That legislation also requires the Commission to conduct continuing studies and investigations of deaths, injuries, diseases, other health impairments, and economic losses resulting from incidents involving consumer products. The Commission obtains information about product-related deaths, injuries and illnesses from a variety of sources, including newspapers, death certificates, consumer complaints, and medical facilities.
The Commission also operates a surveillance system known as the National Electronic Injury Surveillance System (NEISS) that provides timely data on consumer product-related injuries treated in a statistically valid sample of hospital emergency departments in the U.S. The Commission also collects information on childhood poisonings through the NEISS system, in support of the Poison Prevention Packaging Act of 1970.
From these sources, the Commission staff selects cases of interest for further investigation by face-to-face or telephone interviews with persons who witnessed or were injured in incidents involving consumer products. On-site investigations are usually made in cases where the Commission staff needs photographs of the incident site, the product involved, or detailed information about the incident. This information can come from face-to-face interviews with persons who were injured or who witnessed the incident, as well as contact with state and local officials, including police, coroners and fire investigators, and others with knowledge of the incident.
2. Use and sharing of collected information and impact on privacy
The Commission uses this information to support development and improvement of voluntary standards; proceedings for the development of mandatory standards and regulations; information and education campaigns; and administrative and judicial proceedings for enforcement of the statutes, standards, and regulations administered by the Commission. By these means, the Commission removes unsafe products from channels of distribution and consumers' homes and provides information to the public about the safety of consumer products.
3. Use of information technology (IT) in information collection
All NEISS data are reported electronically, and NEISS respondents directly submit data to CPSC through the internet on laptops provided by CPSC. Information for follow-up investigations from NEISS and other sources are collected through traditional face-to-face or telephone interviews with consumers, witnesses, and other knowledgeable parties such as fire, police, and healthcare professionals. Over 85 percent of the follow-up investigations are conducted over the phone.
4. Efforts to identify duplication
There is no other national surveillance system of product-related injuries or childhood poisonings treated in emergency departments. The detailed information obtained from hospital emergency records about incidents associated with consumer products is not available from any other source.
5. Impact on small business
This collection of information is voluntary and does not have an impact on small businesses.
6. Consequences to Federal program or policy activities if collection is not
conducted or is conducted less frequently
If this information were not collected or were collected less frequently, the Commission would lack timely and detailed information to identify new hazards and to support rulemaking proceedings, efforts to develop or improve voluntary standards, actions to obtain correction of products that present a substantial product hazard, and informational campaigns.
7 (a). Special circumstances requiring respondents to report information more
often than quarterly or to prepare responses in fewer than 30 days
Timely reporting of product-related injuries and childhood poisonings treated in emergency departments is necessary to identify, investigate, and respond to new or changing hazards. In FY2012, 54% of the NEISS records were received within 6 days of treatment and 90% within 21 days.
7 (b). Special circumstances requiring the use of a statistical data classification that has not been reviewed and approved by OMB
NEISS does not currently collect information on race and ethnicity in the format recommended by OMB. Race is collected using OMB’s recommended categories under a variable called ‘RACE’. Ethnicity and a free text response to race are collected under a variable called ‘RACEOTH’.
8. Agency’s Federal Register Notice and related information
A notice in the Federal Register was published May 7, 2013. (78 FR 26618) No comments were received.
9. Decision to provide payment or gift
NEISS respondents enter into contracts with CPSC and are compensated for their efforts. See Section 12(a) for details of the estimated burden and costs. A number of persons are contacted through a telephone interview to provide further information about selected injuries or incidents associated with consumer products of special interest to CPSC. See Section 12(b) for details of the estimated burden and costs. In general, respondents are not compensated for participating in a telephone interview. However, we may pay up to 500 people per year at $25 - $50 per response.
10. Assurance of confidentiality
If a person requested to provide information about a product-related injury or incident claims that any information submitted to the Commission is trade secret or confidential business information, that information is subject to the Commission's procedures for withholding confidential information from public disclosure codified at 16 C.F.R. Part 1015, subpart B. If such information is requested under provisions of the Freedom of Information Act, the person who provided the information is notified and given the opportunity to respond and seek judicial relief prior to the Commission's release of the information. In addition, any accident or investigation report made under the CPSA by an officer or employee of the Commission shall be made available to the public in a manner that will not identify any injured person or any person treating him, without the consent of the person so identified.
11. Questions of a sensitive nature
The Commission’s staff takes care to design interview guides so that persons who witness or are injured in incidents associated with consumer products are not requested to provide any information of a sensitive nature.
12 (a). Estimate of hour burden to NEISS respondents
The NEISS system collects information on consumer-product related injuries from about 100 hospitals in the United States. Respondents to NEISS include hospitals that directly report information to NEISS, and hospitals that allow access to a CPSC contractor who collects the data. Collecting emergency department records for review each day takes about 10 minutes. Each record takes about 15 seconds to review. Coding and reporting records that involve consumer product related injuries takes about 2.5 minutes per record. Respondents also spend about 36 hours per year in related activities (training, evaluations, and communicating with other hospital staff).
In FY2012, there were 150 NEISS respondents (total hospitals and CPSC contractors). These NEISS respondents reviewed an estimated 4.6 million emergency department records and reported 400,000 consumer-product related injuries of which 5,100 were childhood poisoning-related injuries. The total burden hours for FY2012 are estimated to be 41,300. The average burden hour per hospital is 430 hours. However, the total burden hour on each hospital varies due to differences in size of the hospital (e.g., small rural hospitals versus large metropolitan hospitals). Therefore, the smallest hospital reported approximately 150 cases with a burden of about 50 hours, while the largest hospital reported over 17,500 cases with a burden of almost 1,400 hours.
The total costs to NEISS respondents for FY2012 are estimated to be $1.7 million per year. NEISS respondents enter into contracts with CPSC and are compensated for these costs. The average cost per respondent is estimated to be about $17,600. The average cost per burden hour is estimated to be $41 per hour (including wages and overhead. However, the actual cost to each respondent varies due to the type of respondent (hospital versus CPSC contractor), size of hospital, and regional differences in wages and overhead. Therefore, the actual annual cost for any given respondent may vary between $1,000 at a small rural hospital and $78,000 at a large metropolitan hospital.
12 (b). Estimate of hour burden to other respondents
The staff conducts face-to-face interviews of approximately 550 persons each year. On average, an on-site interview takes about 4.5 hours. The staff also conducts about 3700 in-depth investigations by telephone. Each in-depth telephone investigation requires approximately 20 minutes.
The Commission staff estimates that this collection of information imposes a total annual hourly burden of 3,708 hours on all respondents: 2,475 hours for face-to-face interviews; 1,233 hours for in-depth telephone interviews.
The Commission’s staff estimates the value of the time required for reporting is $27.12 an hour (U.S. Bureau of Labor Statistics, “Employer Costs for Employee Compensation,” December 2012, Table 9, Total compensation for all sales and office workers in goods-producing industries: http://www.bls.gov/ncs). At this valuation, the estimated annual cost to the public is about $100,570.
13. Estimate of other total annual cost burden to respondents or recordkeepers
The only costs to respondents from this collection of information are those described in item 12, above.
14. Estimate of annualized costs to the Federal government
The annual cost to the government of the collection of the NEISS information is estimated to be about $3.3 million a year. This estimate includes $1.7 million in compensation to NEISS respondents described in section 12(a) above. This estimate also includes $1.6 million for about 160 professional staff months each year. The estimate of professional staff months includes the time required to: oversee NEISS operations (e.g., administration, training, quality control); prepare questionnaires, interviewer guidelines, and other instruments and instructions used to collect the information; conduct face-to-face and telephone interviews; and evaluate responses obtained from interviews and completed forms. Each month of professional staff time costs the Commission about $10,174. This is based on a GS-12 mid-level salaried employee. The average yearly wage rate for a mid-level salaried GS-12 employee in the Washington, DC metropolitan area (effective as of January 2011) is $84,855 (GS-12, step 5). This represents 69.5 percent of total compensation (U.S. Bureau of Labor Statistics, “Employer Costs for Employee Compensation,” December 2012, Table 1, percentage of wages and salaries for all civilian management, professional, and related employees: http://www.bls.gov/ncs/). Adding an additional 30.5 percent for benefits brings average yearly compensation for a mid-level salaried GS-12 employee to $122,094.
15. Program changes or adjustments
This request for the approval of an estimated 45,008 (41,300 NEISS and 3,708 other) burden hours per year is a decrease of 4,697 hours since this collection of information was last approved by OMB in 2009. This decrease is due in part to the increased proportion of investigations being conducted by phone. This information request collection excludes the burden associated with other publicly available Consumer Product Safety Information Databases, such as internet complaints, Hotline, and MECAP reports.
16. Plans for tabulation and publication
The Commission provides yearly reports of NEISS data to the public on its website. NEISS data are also available for public use through the CPSC website. The Commission publishes results from some of its investigations of product-related injuries and incidents in Federal Register notices during rulemaking proceedings, and in safety alerts, news releases, and other informational materials that are disseminated to the general public, voluntary standards groups, firms, and trade associations. The Commission has no specific plan to publish all of the data obtained from this collection of information.
17. Rationale for not displaying the expiration date for OMB approval
Not applicable.
18. Exception to the certification statement
Not applicable.
B. Collection of Information Employing Statistical Methods
1. The potential respondent universe consists of patients treated in statistically selected hospitals participating in NEISS to report emergency department treated product-related injuries, and individuals involved with incidents recorded in newspaper articles, consumer complaints, death certificates, coroner reports and any other injury sources which may be reported to the Commission.
The affiliated NEISS hospitals report more than 400,000 consumer product related cases annually to the Commission using existing information extracted from hospital records. Since these data are limited, further information is frequently necessary, and approximately 1,200 of these cases are selected for investigation via telephone or face-to-face. Other data sources contribute over 56,000 cases, of which approximately 1,800 are selected for investigation.
2. Cases associated with categories of interest are selected daily from the hundreds of incident reports received each day by the Commission. Commission investigators call to interview or to arrange to visit the victim or others to determine specific details about the accident sequence. Information collected from the victim, family member, witness, or others is reported on an investigation form designed for this purpose.
When less than 100 percent of the surveillance cases are selected for investigation, the universe of cases is stratified by relevant factors such as type of injury or consumer product involved and a simple random sample of cases is selected.
The estimation procedure for probability surveys involves multiplying the original surveillance case weight by the case weight appropriate for the follow-back investigation. Normally, the latter is the reciprocal of the probability of selection, adjusted where needed for non-response.
3. About 76 percent of the victims involved in the selected accidents are successfully contacted. Of those contacted, about 95 percent agree to voluntarily provide information on the accident situation. For probability surveys, responses are weighted to account for non-responses. The results from probability surveys can be generalized to the universe studied.
4. No tests of procedures or methods will be undertaken.
5. Contact for collection and analysis of NEISS data:
Thomas Schroeder U.S. Consumer Product Safety Commission
4330 East West Highway
Bethesda, MD 20814
301-504-7431
Consultants originally involved in the statistical design of the National Electronic Injury Surveillance System:
Joseph Waksbergh Westat, Inc. (deceased)
J. Michael Brick 1650 Research Blvd.
David Marker Rockville, Maryland 20850, 301-251-1500
File Type | application/msword |
Author | lglatz |
Last Modified By | RSquibb |
File Modified | 2013-07-18 |
File Created | 2013-04-22 |