Wednesday, July 29, 2009

Compliance News: Novel Influenza A (H1N1): Swine Flu and You

By Dean H. Samet, CHSP

On June 11, 2009, the World Health Organization signaled that a global pandemic of novel influenza A (H1N1) was underway by raising the worldwide pandemic alert to Phase 6 as a reflection of the spread of this virus, not the severity of illness caused by the virus. Most of us have been informed and warned about this new so-called “swine flu” virus first detected in people in the United States in April of 2009. The Centers for Disease Control and Prevention (CDC) has determined that this now named novel influenza A (H1N1) flu virus is contagious and spreading from person to person the same way regular seasonal influenza viruses spread - primarily by the coughing and sneezing of those infected with the virus. What can you do to stay healthy?

If you have what feels like seasonal flu symptoms, e.g., fever, cough, sore throat, runny or stuffy nose, body aches, headache, chills, fatigue, possibly diarrhea, and vomiting, you might be infected with the H1N1 virus. The CDC suggests:

• Stay informed via the CDC website (www.cdc.gov/h1n1flu).
• Cover your nose and mouth with a tissue when you cough or sneeze. Then throw the tissue in the trash after you use it.
• Wash your hands often with soap and water for 15 to 20 seconds, especially after you cough or
sneeze.
• Use alcohol-based hand cleansers or disposable hand wipes.
• Avoid touching your eyes, nose or mouth. You may have touched something with flu viruses on it. Germs spread that way.
• Try to avoid close contact with sick people.
• Stay home if you get sick except to seek medical care. The CDC recommends that you stay home from work or school and limit contact with others to keep from infecting them.
• If you have severe illness or you are at high risk for flu complications, contact your health care
provider or seek medical care.
• Stay home if you are sick for seven days after your symptoms begin or until you have been
symptom-free for 24 hours, whichever is longer.
• Follow public health advice regarding school closures, avoiding crowds and other social distancing measures.
• Call 1-800-CDC-INFO for more information.

Furthermore, the CDC recommends urgent medical attention for children experiencing the following emergency warning signs:

• Fast breathing
• Bluish or gray skin color
• Not drinking enough fluids
• Severe or persistent vomiting
• Not waking up or not interacting

• Being so irritable that the child does not want to be held
• Flu-like symptoms improve but then return with fever and worse cough

In adults, emergency warning signs that need urgent medical attention include:

• Difficulty breathing or shortness of breath
• Pain or pressure in the chest or abdomen
• Sudden dizziness
• Confusion
• Severe or persistent vomiting
• Flu-like symptoms improve but then return with fever and worse cough

The United States continues to report the largest number of novel H1N1 cases of any country worldwide. According to the CDC, as of July 17, 2009 there have been 40,617 reported cases of H1N1 flu infection in all 50 states, including the District of Columbia, and American Samoa, Guam, Puerto Rico, and the US Virgin Islands, and 263 deaths as a result of illness associated with this virus. A July 6th World Health Organization (WHO) update showed 94,512 confirmed cases in 122 countries with 429 deaths. The good news is that most people who have become ill have recovered without requiring medical treatment.

CDC anticipates that there will be more cases in the United States over the summer and into the fall and winter this year. By following the above-listed CDC suggestions and everyday actions, you can help prevent the spread of germs that cause respiratory illness like the H1N1 flu virus and that will permit you, your family, fellow workers, and those around you to stay healthy!

Friday, May 29, 2009

Compliance News: Temporary Lighting

By Robert Trotter, CBO, CFM

Wiring for power and lighting during a period of construction, remodeling, maintenance, repair, or demolition, and similar purposes must comply with the provisions of NFPA 70 National Electrical Code, 1999 edition. Under the requirements of section 305-3 temporary electrical power and lighting installations are permitted during the period of construction, remodeling, maintenance, repair, or demolition of buildings, structures, equipment, or similar activities.

Temporary electrical power and lighting installations are permitted for a period not to exceed 90 days for Christmas decorative lighting and similar purposes. Temporary wiring must be removed immediately upon completion of construction or purpose for which the wiring was installed.

Compliance News: Fusible Links for Fire Doors

By Robert Trotter, CBO, CFM

Fusible links often play an important role for fire door operation. NFPA 80, Standard for Fire Doors and Fire Windows, 1999 edition, describes the provisions for the use of fusible links. First it is important to understand that a fusible link is two pieces of metal held together by low-melting-point solder. Horizontally sliding doors, vertically sliding doors, rolling steel doors and service counter doors of the rolling type must close automatically upon activation or release of a fusible link or detector. In reference to the example pictured, section 1-10.2 states, “All detectors including fusible links shall not be placed in the dead air space developed at the intersection of the wall and ceiling directly above the fire door.” The dead air space is measured four inches down from the ceiling to the closest edge of the fusible link or four inches along the ceiling extending outward from the corner. NFPA 80 also requires detectors or fusible links to be installed on both sides of the wall, interconnected so that the operation of any single detector or fusible link causes the door to close. Where fusible links are used, one fusible link must be located near the top of the opening, and additional links shall be located at or near the ceiling on each side of the wall. Fusible links located above the ceiling are not acceptable. Refer to NFPA 80 for full text and exceptions.

Compliance News: BMP: An ISO 9001 Process Approach?

By Arthur J. Mahanna, Architect

In 1999 The Joint Commission (TJC) issued a revised Statement of Conditions (SOC) document that included a Building Maintenance Program option for Healthcare occupancies under the Part 3, Life Safety Assessment, questions 6I (new) and 6J (existing). This option provided hospitals scoring benefits for ten specific items prone to failure if they could demonstrate they had implemented an effective Building Maintenance Program (BMP). These included specific issues related to fire doors, smoke doors, corridor doors, smoke barriers, corridor walls, exit signs, egress lights, trash and linen chutes, ice and snow removal in the means of egress, and grease producing devices.

By their definition, if a hospital could show a 95% effectiveness rating for these issues, a BMP would be considered effective. What this really meant for example, was that if on the day of the Environment of Care (EOC) inspection, the hospital had a few exit signs burned out, a Requirement for Improvement (RFI) would not be received for each exit sign if you could produce the appropriate inspection and analysis information for a BMP on your exit signs.

For the next 12 years people analyzed, discussed, and microscopically dissected what TJC meant by 95% and the many different ways this data could be reported and managed. In many cases the emphasis was on how to get the scoring benefit rather than the actual reason for the BMP. As a result, the Centers for Medicare & Medicaid Services (CMS), and even some TJC Life Safety Code Specialist Surveyors, would not accept BMP as a legitimate substitute for 100% compliance at all times.

In January of 2009, TJC released its new Hospital Accreditation Standards (HAS) as part of their standards improvement initiative. While this new document mentioned BMP as an effective method for ensuring compliance, the scoring benefits were eliminated. On the surface this may have seemed like TJC was backing off the need for such programs, but in reality for those who truly had taken the BMP concept to heart, the value beyond scoring was clear. Not only does BMP serve as a valuable tool in reducing the risk of RFIs, it also can be used to support a hospital when RFIs and possible Conditional Accreditation become a reality.

In eliminating the scoring, TJC has actually opened up the use of this concept for many more items previously excluded from the BMP methodology. For example, in the 2009 Hospital Accreditation Standards, per Standard EC.02.03.05, “The hospital maintains fire safety equipment and fire safety building features.” Numerous tests and inspections are required, such as: quarterly testing of supervisory signals; semi-annual testing of valve tamper switches and water flow devices; and monthly inspections of fire extinguishers. In particular, items like these, with large volumes of devices to inspect and test, lend themselves well to the BMP concept. This also holds true for some items per Standard EC.02.05.07, “The hospital inspects, tests, and maintains emergency power systems,” e.g., battery operated egress lights, or Standard EC.02.05.09, “The hospital inspects, tests, and maintains medical gas and vacuum systems.”

In addition, if someone is inspecting traditional BMP items such as fire or smoke doors, why not add a check for unauthorized coverings and decorations or even unapproved protective plates at the same time the closers, latches, gaps and undercuts are reviewed?

Interestingly, fire walls were never part of the original ten BMP items. The reason given during the original BMP development process was that fire walls needed to be 100% compliant all the time. While this does emphasize the importance of maintaining fire walls, the words do little to actually ensure 100% compliance. Only a “process approach” to managing these items can truly reduce the possibility of failures and the likelihood of an RFI.

While a “process approach” can assist in the accreditation process with The Joint Commission, this methodology also fits quite nicely with the ISO 9001 standards adopted by Det Norske Veritas Healthcare (DNVHC), the new accrediting body approved last year by the Centers for Medicare & Medicaid Services.

Per ISO 9001, 0.2 Process Approach:

“This International Standard promotes the adoption of a process approach when developing, implementing and improving the effectiveness of a quality management system, to enhance customer satisfaction by meeting customer requirements.

For an organization to function effectively, it has to identify and manage numerous linked activities. An activity using resources, and managed in order to enable the transformation of inputs into outputs, can be considered as a process. Often the output from one process directly forms the input to the next.

The application of a system of processes within an organization, together with the identification and interactions of these processes, and their management, can be referred to as the ‘process approach’.”

An advantage of the process approach is the ongoing control that it provides over the linkage between the individual processes within the system of processes, as well as over their combination and interaction.

When used within a quality management system, such an approach emphasizes the importance of:
a) Understanding and meeting requirements,
b) The need to consider processes in terms of added value,
c) Obtaining results of process performance and effectiveness, and
d) Continual improvement of processes based on objective measurement.

NOTE: In addition, the methodology known as “Plan-Do-Check-Act” (PDCA) can be applied to all processes. PDCA can be briefly described as follows.

Plan: Establish the objectives and processes necessary to deliver results in accordance with customer requirements and the organization’s policies.

Do: Implement the processes.

Check: Monitor and measure processes and product against policies, objectives and requirements for the product and report the results.

Act: Take actions to continually improve process performance.

Note the similarities between a Building Maintenance Program and the “Process Approach” described in the ISO standards:

• “Planning” a BMP requires identifying the locations and quantities of fire doors, smoke doors, etc., within your facility and identifying what requirements should be evaluated for each item.

• “Doing” a BMP involves inspecting the requirements for each item and recording when a specific requirement is non-compliant.

• “Checking” a BMP involves reviewing findings and analyzing the survey results for problem areas.

• “Acting” on BMP results means that the 95% rule can still be used as a means of evaluating success as well as determining where improvements are needed. If the closers and latches on a particular set of fire doors continue to fail, you should determine the reasons for the failure and correct. Perhaps training staff that use carts is warranted. Or, if inspecting fire doors quarterly simply isn’t resulting in a 95% rating, then it may be necessary to conduct monthly inspections of fire doors, or perhaps monthly inspection of fire doors in certain areas.

Another critical aspect of a BMP’s success is your work order repair process. As described earlier, “An advantage of the process approach is the ongoing control that it provides over the linkage between the individual processes within the system of processes, as well as over their combination and interaction.” Another possible cause for continued failure of the same items over and over again is a failure to repair items. Since the BMP and work order repair processes are ultimately linked together, the BMP can help to determine the success of the work order repair process.

Regardless of the AHJ you choose now or in the future, a process approach that follows the ISO “Plan-Do-Check-Act” methodology and/or BMP will improve your quality management system and ultimately reduce problems in future accreditation surveys and inspections. BMP is alive and well for those wise enough to see its benefits.

Sunday, March 29, 2009

Compliance News: Noncombustible Sills for Fire Doors

By Robert Trotter, CBO, CFM

Fire rated doors must be installed properly so that fire cannot spread below, around, or above the door. To minimize the risk for fire spread at the undercut of a fire door, NFPA 80, Standard for Fire Doors and Fire Windows, 1999 edition describes the requirements for sills. Section 1- 1.2.1 states, “In buildings with noncombustible floors, special sill construction shall not be required, provided the floor structure is extended through the door opening.” Largely, healthcare occupancies have noncombustible floor construction and no special sill construction would be required. This means the example pictured would be compliant even though the carpet extends through the door opening. However, Section 1-11.2.3 states, “Combustible floor coverings shall not extend through openings protected by 3-hour rated fire protection door assemblies.”

In buildings with combustible floors or combustible floor coverings, special sill construction is required if the floor structure is extended through the door opening, as combustible floor construction is not permitted to extend through the door opening except door openings required to be protected by 20- or 30-minute doors. All sills must be constructed of noncombustible materials. Consult NFPA 80 for additional details regarding the arrangement of sills.

Compliance News: Unusual Observations

By Robert Trotter, CBO, CFM

Whether you complete your own life safety assessment for compliance with the Life Safety Code® or the work is performed by a third party, frequently an issue is discovered that is not described in the Statement of Conditions™. For the past several years we have been noting these issues as Unusual Observations. Starting in January 2009, as a result of The Joint Commission Standards Improvement Initiative, the new Life Safety Chapter incorporates an Element of Performance at the end of each individual standard to note other deficiencies. For example, under the Hospital Accreditation Program Standard LS.02.01.20 EP (32) states, “The hospital meets all other Life Safety Code means of egress requirements related to NFPA 101- 000: 18/19.2.” This Element of Performance gives you the latitude to create a Work Order or a Plan for Improvement (PFI) for any deficiency discovered that can not be associated with one of the Standard’s preceding Elements of Performance.

Regarding the example photograph, the Hospital Standard does offer Element of Performance (13) relative to the exit discharge and obstructions or impediments to the public way that may be acceptable for the landscape in the means egress. However, the full text and exceptions sends you NFPA 101-2000: 7.1.10.1 for means of egress reliability. Another key observation that may not be discernible in the photograph is the change in elevation in excess of 21 inches without a ramp or stair as required by NFPA 101-2000: 7.1.7.2. This would be an excellent example of when to cite noncompliance at LS.02.01.20 EP (32).

Compliance News: Magnetic Locks Create Headroom Obstruction

By Robert Trotter, CBO, CFM

As pictured in the example, magnetic locks installed to control access or egress often are located in a position that creates a headroom obstruction. According to section 7.2.1.2.2 of the NFPA 101®, Life Safety Code®, 2000 edition, “Projections into the required clear door opening width that are not less than 34 inches but that do not exceed 80 inches above the floor or ground shall be limited to the hinge side of each door opening and shall not exceed 4 inches.” This space allows for projections such as self-closing or automatic-closing devices, panic hardware and fire exit hardware. Projections exceeding 80 inches above the floor or ground are not limited.

Compliance News: Stair Identification Signs

By Michael L. Hawkins, CFSI, CHMT

All too often when conducting SOC surveys in Health Care Occupancies, we come across improper stair identification. NFPA 101 Life Safety Code®, 2000 ed., Chapter 19 “Existing Healthcare” requirements refers back to Chapter 7 “Means of Egress” for proper stair identification.

NFPA 101®, Life Safety Code® 2000 edition
7.2.2.5.4* Stair Identification Signs
Stairs serving five or more stories shall be provided with signage within the enclosure at each floor landing. The signage shall indicate the story, the terminus of the top and bottom of the stair enclosure, and the identification of the stair enclosure. The signage also shall state the story of, and the direction to, exit discharge. The signage shall be inside the enclosure located approximately 5 feet (1.5 m) above the floor landing in a position that is readily visible when the door is in the open or closed position.

7.2.2.5.5 Egress Direction Signs
Wherever an enclosed stair requires travel in an upward direction to reach the level of exit discharge, signs with directional indicators indicating the direction to the level of exit discharge shall be provided at each floor level landing from which upward direction of travel is required. Such signage shall be readily visible when the door is in the open or closed position.

Exception No. 1: This requirement shall not apply where signs required by 7.2.2.5.4 are provided.
Exception No. 2: Stairs extending not more than one story below the level of exit discharge where the exit discharge is clearly obvious shall not be subject to this requirement.

Stairwell signage is extremely important not only for the evacuation of occupants but for the responding fire and rescue personnel. Please check those in your hospital to ensure that the needed and appropriate signs are in place.

Compliance News: Power Strips in Patient Care Areas

By David Stymiest, PE, CHFM, FASHE, CEM, GBE

A subject that bears watching is the current concern about stand-alone power strips being used in General Patient Care Areas and Critical Patient Care Areas. ASHE/AHA Listserv users saw considerable traffic recently on this topic. The issue stems from a Centers of Medicare and Medicaid (CMS) document (Publication 100-07, Transmittal 27 dated August 17, 2007, entitled Revisions to Appendix PP – Guidance to Surveyors for Long Term Care Facilities) that includes the following excerpt: “Power strips may not be used as a substitute for adequate electrical outlets in a facility. Power strips may be used for a computer, monitor, and printer. Power strips are not designed to be used with medical devices in patient care areas.” Some hospitals are reporting that CMS hospital surveyors have used this LTC Facility guidance to cite them for using power strips (called “Relocatable Power Taps” in UL terminology) in General Patient Care Areas and Critical Patient Care Areas.

It appears that this issue arose because of Underwriters Laboratories’ (UL’s) concern that there are no listed power taps for patient care areas of health care facilities per UL product category “Relocatable Power Taps (XBYS).” UL stated in a March 1, 2008 posting on the International Association of Electrical Inspectors (IAEI) website www.iaei.org, “The use is restricted from these patient care areas because UL cannot control what is connected to the power taps which could result in leakage current that would be in excess of what is permitted for patient care areas of hospitals.” UL further stated that “UL does Classify complete system medical cart assemblies for use in hospitals under the product category “Medical Equipment (PIDF).” Those medical cart assemblies may contain a power tap as part of the tested assembly per UL 60601-1 Medical Electrical Equipment (previously UL 2601-1.) Interpreting UL’s statements, it appears that external equipment (that not already tested as part of the listing process) may not be plugged into the cart-mounted power strips.

Some hospitals are taking the risk assessment approach to this issue – that is recognizing that power strips, or relocatable power taps, are subject to failure just like any other device and therefore inventorying them and subjecting them to the same risk-based testing and maintenance regimens as outlets and medical devices.

Stay tuned to ASHE’s ongoing advocacy efforts – this subject is likely to continue to be part of those efforts due to its potential cost impact on America’s hospitals.

As always, regardless of the area in which such devices are used, facilities need to be aware of the total loading of devices plugged into them and ensure that the portable devices themselves, and the branch circuits that feed them, do not become overloaded. If power strips are presently being used, regardless of the area, high current-draw equipment should not be plugged into them.

Thursday, January 29, 2009

Compliance News: TJC Standards and Scoring Changes for 2009

There have been some significant changes to The Joint Commission’s (TJC) standards and scoring for 2009. The Emergency Management (EM) requirements have been removed from the Environment of Care chapter and incorporated into their own EM chapter. The Life Safety Code® requirements, Statement of onditions™ (SOC™), and Interim Life Safety Measures (ILSM) have all been relocated to a new Life Safety (LS) chapter. While there are purportedly no new requirements as a result of all these changes, there are some subtle nuances that may be viewed as new requirements along with items that might have been implied in the past which are now specified. However, the most significant changes can be found in the scoring.

Compliance News: TJC Thresholds to Serve as Screens for PDA & CA Decisions

By Dean Samet, CHSP

In their December 2008 The Joint Commission Perspectives, Volume 28, Number 12, The Joint Commission (TJC) reported that at its October 2008 meeting, TJC’s Accreditation Committee (AC) approved the remaining component for the 2009 accreditation decision methodology which included elimination of the use of thresholds” as determinants of Conditional Accreditation (CA) and Preliminary Denial of Accreditation (PDA). Thresholds have been used by TJC for years to determine whether to invoke or recommend CA or PDA if and when an organization had exceeded a preset number of Requirements for Improvement (RFIs).

Compliance News: Sprinkler Obstructions

By Robert Trotter, CBO, CFM

The Joint Commission’s Life Safety Standard LS.02.01.10 states, “…buildings contain approved automatic sprinkler systems as required…” In order to determine where sprinklers are required facility managers should consult NFPA 13, Standard for the Installation of Sprinkler Systems.  Recently, TJC surveyors have recognized deficiencies related to sprinkler obstructions and noted such observations.  NFPA 13 states, “Sprinklers shall be installed under fixed obstructions over 4 foot wide such as ducts, decks, open grate flooring, cutting tables, and overhead doors.  Sprinklers are not required under obstructions that are not fixed in place such as conference tables.” The example shows sprinkler protection under an HVAC duct which was an obstruction that prevents sprinkler discharge from reaching the hazard.  Consult your licensed fire sprinkler contractor for assistance.

Compliance News: Beyond Level of Exit Discharge

By Robert Trotter, CBO, CFM

NFPA 101®, Life Safety Code® states in section 7.7.3 “Stairs shall be arranged so as to make clear the direction of egress to a public way.  Stairs that continue more than one-half story beyond the level of exit discharge shall be interrupted at the level of exit discharge by partitions, doors, or other effective means.”  The example shown is a barrier that restricts downward travel.  Upward travel to the rooftop may also require a barrier.  The LSC also prescribes provisions for signs.  Section 7.10.8.3.1 states,  “Any door, passage, or stairway that is neither an exit nor a way of exit access and that is located or arranged so that it is likely to be mistaken for an exit shall be identified by a sign that reads as follows: NO EXIT.”  The NO EXIT sign shall have the word NO in letters two inches high, with a stroke width of ⅜ inch, and the word EXIT in letters one inch high, with the word EXIT below the word NO, unless such sign is an approved existing sign.  The sign in the example may be an approved existing sign as it appears to be meeting the intent of the code.

Compliance News: Storage in Exit Enclosures

By Robert Trotter, CBO, CFM

Maintaining the means of egress is a critical role for any facility manager.  It is important to note that NFPA 101®, Life Safety Code® section 7.2.2.5.3.1 addresses storage in exit enclosures,“Open space within the exit enclosure shall not be used for any purpose that has the potential to interfere with egress.”  Clearly by
the examples shown, this storage arrangement has the potential to interfere with egress by leaving this stairway completely inaccessible should these stored materials catch on fire. Moreover, it also presents an opportunity for an incendiary fire.

Compliance News: Combustible Decorations

By Robert Trotter, CBO, CFM


Evaluation of combustible decorations is always difficult because interpretation of the requirement is subjective.  One person may believe the decorations are acceptable and do not constitute a hazard, while another may feel that the decorations are too much.  Regardless, combustible decorations must meet the requirements of the Life Safety Code®. For those organizations accredited by The Joint Commission, requirements for combustible decorations are found in the Life Safety Chapter. For example, the hospital accreditation program Standard LS.02.01.70 Element of Performance (1) states, “The hospital prohibits all combustible decorations that are not flame retardant. (For full text and any exceptions, refer to NFPA 101-2000: 18/19.7.5.4.)”  Both the new and existing health care occupancy chapters state, “Combustible decorations shall be prohibited in any health care occupancy unless they are flame-retardant. Exception:  Combustible decorations, such as photographs and paintings, in such limited quantities that a hazard of fire development or spread is not present.”