Vehicular based drug box temperature control study
Vehicular Based Drug Box Temperature Control Study A Research Project Presented to the Department of Occupational and Technical Studies Old Dominion University In Partial Fulfillment of the Requirement for the Degree of Master of Science in Occupational and Technical Education Jonora Mejia Winter, 2006 APPROVAL PAGE
This project was prepared by Jonora D. Mejia under the direction of Dr. John Ritz
in OTED 636, Problems in Education, as partial fulfillment of the requirements for the
degree of Master of Science in Occupational and Technical Education.
Date:______________________ Approved by______________________________
ACKNOWLEDGMENT
This study on the temperature variation in the Verde Valley paramedic drug boxes
would not have been possible without the efforts and documentation by the A shift EMS
crews at Verde Valley Fire District, Verde Valley Ambulance Company and Sedona Fire
District. Their consistent and accurate documentation made this project a reality. The
author also wished t to acknowledge all the guidance and time provided by her OTED
TABLE OF CONTENT
Acknowledgement……………………………………………………………ii Table of Tables…………………………………………………………….v Table of Figures.vi Chapter
A. Storage Factors Affecting Medication Stability. 15
B. United States Pharmacopoeia Recommendations
C. Products Currently Available to Provide a Temperature
D. Attempts to Improve Out of Hospital Medication
V. SUMMARY, CONCLUSIONS AND RECOMMENDATIONS.35
REFERENCES. 37
TABLE OF TABLES TABLE OF FIGURES Figure 1. -Verde Valley Fire District min/max control temperatures. 28 Figure 2. - Verde Valley Fire District min/max experimental temperatures. 28 Figure 3. – Verde Valley Ambulance min/max control temperatures. 29 Figure 4. – Verde Valley Ambulance min/max experimental temperatures. 29 Figure 5. – Sedona Fire District min/max control temperatures. 30 Figure 6. – Sedona Fire District min/max control temperatures. 31 Figure 7. – Maximum control ranges. 32 Figure 8. – Minimum control ranges. 32 Figure 9. – Maximum experimental ranges. 33 Figure 10. – Minimum experimental ranges. 33 CHAPTER I INTRODUCTION
All paramedic drug boxes in the Verde Valley area of Northern Arizona are stored
in one of two paces; either on an ambulance in a designated compartment or on a rescue
truck of a local fire agency. The Verde Valley is located in the northern half of Arizona
in a high desert area that experiences wide swings of temperatures from 10º F. in the
winter months to well over 110º F. during the summer. These temperature variations
expose the medications in the drug boxes t temperatures both higher and lower than
storage temperatures recommended by the drug manufacturers. Storage of these
medications under less than ideal conditions can mean shortened expiration dates or even
lessening of the effectiveness of the medications. The first possibility impacts patient care
by adding to overall health care costs by increasing frequency of medication replacement
in the drug boxes. The second has the possibility to impact patient care in a more direct
manner. medications stored in an uncontrolled environment have the potential to degrade
in potency; this could mean ineffective or even dangerous treatment for the patient
receiving the medications (Thermal Engineering, 2004).
In 2005 the Arizona Department of Health Services (ADHS) medical drug box
committee proposed a change in Arizona Revised Statue designed to require all
prehospital drug boxes to be temperature controlled by January 6, 2009. In March of
2006 the committee elected to remove this proposed change from he working draft
(ADHS, 2006). There were several reasons for this decision. First, there is little
information at the present time on what the temperatures are in unprotected drug boxes in
Arizona. As the climate varies from over 115º F. in the southern parts of the state to
below zero in the northern regions, it was recognized that a “one size fits all” solution
would not be workable. Secondly, the committee was unable to arrive at a standardized
temperature range that could be used to determine if each drug box was in compliance.
Thirdly, the cost of retrofitting each drug box in a commercially available temperature
controlled unit was estimated at approximately $3900.00 per unit (Mermaid, 2006). Since
many emergency medical service (EMS) providers in Arizona are volunteer units it was
determined that this type of requirement could constitute financial hardship for at least
Almost all medications have a temperature range recommended for storage by the
manufacturer. Many times it is simply defined as a controlled room temperature
environment (Allegra, Brennan, Lanier, Lavery, & MacKenzie, 1999). Other medications
have more specific requirements such as less than 40º F. this study will begin to look at
the issue of temperature control by first assessing the temperature range in drug boxes
that are stored without any additional insulation or temperature control attempts and then
begin to look at options for temperature control that are readily available and cost
Statement of the Problem
The purpose of this study was to determine temperature variations in prehospital
drug boxes in the Verde Valley area of Arizona during the months of October and
Research Goals
Prehospital drug boxes in the Verde Valley area have never been studied for
minimum and maximum temperature variances. this is now of importance as ADHS has
indicated that there is a strong possibility that there will be a requirement for drug box
temperature control and tracking in the future (ADHS, 2006). The following hypothesis
H1: Temperatures of the prehospital drug boxes will remain in an acceptable range
when stored in a compartment insulated with rigid, solid foam.
Background and Significance
The Verde Valley area of Arizona is situated approximately half way between the
urban Phoenix area and the mountain community of Flagstaff. At approximately 3500
feet in elevation it has temperature swings from 10º F. in the winter to over 110º F. in
the summer. Drug boxes contained in both ambulances and fire trucks are subjected to
these temperature extremes. In the past there have been no requirements to attempt to
regulate the storage temperatures of these drug boxes in spite of the fact that all
medications have a recommended range of storage temperatures from their
manufacturers. Many drugs are tested only at their laboratory’s room air temperature and
no effort is made to test their effectiveness at either cold or hot extremes. (Brown,
Krumperman, & Fullagar, 2004). However, some medications are rendered ineffective
outside a set temperature range. It is suspected that Verde Valley area prehospital drug
boxes may at times fall outside of recommended storage ranges (Allegra et al., 1999).
Following the manufacturer recommendations for all drugs currently in the Arizona drug
box the temperature range should ideally stay between 68-77º F. to safely accommodate
maximum expiration dates on all the drugs.
In 2005 the drug box committee that controls the content of the Arizona
prehospital drug boxes made a recommendation that all Arizona drug boxes be
temperature regulated by January 2009. In spring 2006 this recommendation was
removed from the proposed amendment package (ADHS, 2006). In part this was done in
response to the knowledge that very little was known about current temperature
conditions under which the drug boxes are being stored. It was decided that until more
information was gathered on drug box temperature variances no mandatory regulations
This study has attempted to gather data on the variance in temperature in the drug
boxes in the Verde Valley area of Arizona. This information will help agencies assess
what measures, if any are necessary to limit temperature swings in the their drug boxes
and help them to make decisions on future modifications in storage methods as it seem
quite probable that the issue of drug box temperature control will be raised in the future at
the state level. The data gather in this study will provide a baseline of information that
can be used for comparison when implementing any future interventions directed at
improving temperature control in the prehospital drug boxes.
Limitations
The results of this study can be generalized only to other areas that have the same
winter and summer range of temperature variations as the Verde Valley. Similarly, only
drug boxes which are of similar make and mode would be applicable for comparison.
Finally, all drug boxes in this study were stored on ambulances or rescue trucks that were
housed in a garage or bay when not actively responding to a 9-1-1 call. Ambulances or
rescue trucks housed in other conditions would not be easily generalized to this study.
Assumptions
It was assumed that all drug boxes studied were either Plano or Pelican hard sided
brands. Soft sided models were not included. All boxes were stored in a locked
compartment in either an ambulance or rescue truck. None of the vehicles had
supplemental heating or cooling units on board to regulate drug box temperatures.
Procedures
Data were collected by placing minimum/maximum thermometers inside each
drug box studied. The thermometers were read every third day for three weeks, consistent
with an A-B-C shift rotation and temperatures were recorded in a log. This provided a
baseline of temperature variance in existing compartments. Additional data were then
gathered in the same manner from the same drug boxes after modifications were made
with additions of rigid construction foam insulation. The min/max temperature variants
were collected every third day. The data were compared to see if the modifications
impacted the temperatures of the stored drug box medications.
Definition of Terms
To establish consistent terminology and assist the reader in understanding the study, the
following terms have been defined for use in the paper.
ADHS: Arizona Department of Health Services. The division of Arizona government
which oversees public health related offices and agencies.
Drug box: A rigid, lockable, plastic container used to store the medications allowed for
prehospital use by emergency medical services providers in Arizona.
EMS: Emergency medical services, care provided by EMTs and paramedics via the 9-1-1
system prior to a patient entering a hospital healthcare system.
Expiration date: A date printed on the medication that indicates last day of recommended
Indoor temperature environment: Term used to define common ranges of indoor
temperature found during the testing of medications by the manufacturer. Commonly this
range is designated as from 59º - 86º F.
Minimum/maximum thermometer: Special type of thermometer that measures lowest
attained temperature and highest attained temperature during a predetermined time
period. This thermometer will maintain recording the minimum/maximum range until
Prehospital: The healthcare environment that provides for patient care before arrival at a
hospital, emergency department, or urgent care facility.
Rescue truck: A fire truck manned by personnel wit ES certifications such as EMT or
paramedic that carries equipment such as oxygen, medications, IV solutions, and
bandages that provides patient care at the scene of a 9-1-1 call but does not transport the
patient to a higher level of care such as an emergency room.
Temperature control: Any method that limits variation in temperature and tracks the
Overview of Chapters
Chapter I has reviewed the need for assessment of temperature variance in drug
boxes due to the strong probability of mandated temperature control in the near future.
Chapter II reviews current relevant literature from areas who have already implemented
some forms of temperature control (Mehta, Doran, Lavery, & Allegra, 2002). It will
include exploring the results of research that have made adjustments similar to this
study’s. Chapter III outlines in detail the methodologies and procedures used to gather the
data and specify types of materials and products used in this study. Specifically it
provides detail about insulation materials and thermometers used during this study.
Chapter IV present the results of the temperature logs in detail and looks at trends in
temperature variances during the months of October and November 2006. Chapter V
presents the summary of this study’s results, conclusions derived from the data, and
recommendations for continuing modifications in the management of drug box
CHAPTER II REVIEW OF LITERATURE
This chapter will review the literature concerning the temperature control issue
surrounding out of hospital medication, specifically those carried in ambulances and
rescue trucks. This topic is of interest because while it is well established that most
medications have an optimal temperature range for storage, the medications used in
prehospital emergency services (EMS) are not routinely stored under controlled
conditions (Brown, Krumperman, & Fullagar, 2004). In this chapter the researcher will
review current United States Pharmacopeia (USP) standards and definitions related to
medication storage temperatures and recommendations specific for EMS situations. It
will also look at products currently available which can provide a temperature controlled
environment. Finally, the researcher will review relevant literature from areas who have
already implemented some form of temperature control.
Storage Factors Affecting Medication Stability
Drugs used in the prehospital environment are in principle subject to the same
storage recommendations as hospital based medications with the main stressors being
sunlight, vibrations, and extreme temperatures (Helm, Castner, & Lampl, 2003). These
stressors are not unique to ambulances and rescue trucks. Medications which are shipped
via the mail and then delivered into a mailbox can also experience extreme exposure to
heat. This exposure to heat extremes has been shown to decrease the effectiveness of
certain medications, causing them to deliver inaccurate dosages (Bowman, 2004).
While heat is a known cause of deteriorations, pharmaceutical manufacturers are not
required the USP temperatures at which their products are stable. They are only
required to manufacture products that are stable within the temperature range listed on
the medication package insert (Brown, Krumperman, & Fullagar, 2004).
Approximately 15 years ago Johansen, Schafer, and Brown (1993) exposed four
commonly used out of hospital medications to temperature extremes ranging from -20º to
70º C. with no significant changes in their chemical compositions. The temperature
ranges recommended on these package inserts recommended safe temperatures only from
68º - 77º F. However other studies (Grant, Carroll, & Church et al, 1994; Gottenwald,
Akers, & Liu et al, 1999; Church, Hu & Henry, 1994) have shown degradation of the
quality of medications exposed to temperature extremes.
United States Pharmacopoeia recommendations for Storage
The United States Pharmacopoeia National Formulary prescribes the packaging,
storage and distribution of medication in the United States (Brown, Krumperman &
Fullagar, 2004). These definitions can be both multifaceted and complex (Brown,
Krumperman, and Fullagar, 2004). As an example most medications in the Arizona
prehospital drug box are recommended to be stored between 68º - 77º F. (Table 1). this
temperature range is defined by USP as “controlled room temperature” (USP, 2005). The
definition goes on to quantify this by adding that temperatures can vary intermittently to a
range of 59º - 86º F. It concludes by saying that medication recommended for storage at
controlled room temperature can also be stored in a “cool” temperature which it defines
as any temperature between 46º and 59º F. Using this definition the medications in the
Arizona drug boxes can be stored at temperatures between 46º and 86º F.
Table 1. Paramedic Drug Box Inventory
It is recognized that the out of hospital environment is frequently uncontrolled and
that one of the uncontrolled factors is temperature (Brown, Krumperman, & Fullagar,
2004). In response to this situation the USP has generated EMS specific guidance for
medication storage (Brown & Campagna, 2005). These recommendations include:
o Temperature monitoring devices in the drug boxes to assess and record
o Avoiding temperature extremes by parking emergency vehicles in the shade or
o Developing a program of regular stock rotation with particular attention to
o Using insulated carrying cases for transport and storage of medications.
o Protection from temperatures over 104º F.
o Using the medications with the most stringent storage requirements to determine
storage conditions for mixed loads (Pharmacopeial Forum, 2006).
Using these guidelines and recommendations agencies bear the responsibility to keep
their out of hospital medications within a 40º ranges of temperature changes.
Products Currently Available to Provide a Temperature Controlled Environment.
There are several commercial products on the market in response to the need for a way to
provide temperature control to drugs in and out of the hospital environments. Many focus
on the needs of ambulances and emergency medical service companies. One product is
the Medi-Kool 747 (Mermaid). This is a cabinet design unit made of stainless steel this is
powered by a 12 volt power supply. It can be fitted into a rescue truck or ambulance in an
existing compartment. The dimensions allow for two Pelican brand drug boxes to be
placed inside. Additional features include a stainless steel lock and circuit board that can
be preset to heat and cool. The circuit board also monitors and store up to six months of
data. It requires professional installation and the base model lists for $3900.00.
Advantages are its excellent construction materials, preset circuit board, and generous
inside dimensions. Drawbacks are the power drain on the vehicles battery supply and
high initial cost of purchase and installation.
A second option is the Steady-Temp (Engel). It is also fabricated of stainless steel
and powered by the unit’s 12 volt system. It holds one Pelican brand drug box and
automatically heats and cools to a preset temperature range. Temperature data logger
keys are sold separately from the unit. This unit is designed to be free standing within an
ambulance and does not mount inside an existing cabinet. It does not require professional
installation and lists for $1989.00 Advantages are the lower cost of each unit and smaller
outside dimensions. Disadvantages are the power drain on the vehicle power supply and
the space needed inside the ambulance where space is already at a premium.
A new product called Pharm Guard mounts on the inside of the existing drug box
cabinet and heats or cools the entire compartment, not just the drug box (Biomedical
Equipment & Engineering Services Co.). It is programmed to keep the cabinet
temperature between 59º-75º F. It has a dual power system that ca be run by a 12 volt
vehicle system or by a 120 volt connection. It lists for $2150.00. Advantages are the dual
source power system and the ease of installation into an existing cabinet. The major
drawback is the loss of temperature control each time the compartment is opened.
There are several disadvantages to choosing any of these products. Overall they
all provide temperature control within the range defined as acceptable by the USP.
However, the price per unit may be prohibitive to smaller agencies working with
volunteer or limited budgets. The reliance on 12 volt power coming from the vehicle runs
the risk of draining the unit’s battery system to the extent that the vehicle will not be able
to start up in the event of an EMS service call. This could contribute to a significant delay
in delivering care in an emergent situation. Finally, reliance on a compressor driven
device could result in unknown maintenance and repair costs and possibly take a vehicle
out of service due to a malfunctioning unit.
On the lower tech side of products there are several possible options. Solid foam
insulation can be added to the walls of the drug box compartments. Soft sided coolers
large enough to accommodate the drug box could be used possibly in conjunction with a
refreezable blue ice type product in the warmer months. Using one of these options or a
combination of them has both advantages and disadvantages. One primary disadvantage
is the need to monitor the product through varying temperatures to access the usefulness
of the product it this situation. In addition during the monitoring period, it may be found
that the products do not guarantee temperatures within the accepted range. Advantages
are many: the materials are cost efficient and readily available, they need no special skills
to install or maintain, and they do not place a drain on the vehicle electrical system or on
an agency’s equipment budget. A unique advantage of a soft sided insulated cooler would
be the ability to carry the drug box to a remote or extended scene in a more controlled
Attempts to Improve Out of Hospital Medication Storage Practices
Agencies throughout the United States have begun to make adjustments in their
medication storages practices in the last 15 years. A New Jersey phone survey conducted
in 2000 showed that 85% of programs surveyed had changed their practices in the last
five years based on information from previous research on temperature control (Mehta,
Doran, Lavery, & Allegra, 2002). Changes include adding heating and/or cooling units,
using a temperature monitoring device, planned rotation of medications (Brown, Wojcik,
Bailey & Tran), and adapting policy and procedure documents to reflect the need for
Operations policies established to plan for security and storage of supplies and
medications tend to follow USP EMS specific recommendations. Measures include
procedures such as removing drug boxes from units that are not temperature controlled
and housing them inside the station except when in use, rotating medications in boxes
known to have been exposed to prolonged periods of extreme temperatures, and storing
boxes in designated climate controlled compartments (Virginia Beach Department of
Emergency Medical Services, 02005). Research has prompted some states to amend
regulations to include a requirement that medications should be stored per the
manufacturer’s recommendations (Palmer et al, 1985). It is noted however that simply
requiring this kind of action may be counterproductive if it is not easily achieved and
documented by individual agencies. Palmer et al (1985) notes in a look to the future that
extreme measures such as removal of all medications from ambulances or requiring
immediate installation of active heating and cooling units seem unwarranted. They
advocate an interim policy of encouraging each EMS system to develop a plan of action
aimed toward better understanding of all facets of this issue and towards identifying
the United States emergency medical services community has been aware of the
difficulties in maintaining a controlled environment for medications for over a decade.
This awareness has prompted specific recommendations from the USP for out of hospital
storage conditions. It has also resulted in several companies producing products that can
be used in an ambulance for supplemental heating and cooling.
The State of Arizona has looked at the need to develop standards for temperature
control in drug boxes in this state, most recently in 2006. Decisions on this topic were
delayed to at least 2007 due to lack of information on current temperatures in Arizona
drug boxes and lack of a plan of anion that would be applicable to all EMS agencies in
the state. This study attempts to fill some of the gaps in data by assessing temperature
ranges in the drug boxes located in the Verde Valley area of Arizona.
Chapter III will examine the methods and procedures used to gather the data for
this study. It will also cover the instrument design and details of analysis.
CHAPTER III METHODS AND PROCEDURES
Chapter III contains a description of the methods and procedures needed to collect
the data needed for this study. It includes the population, research variables, field
procedures, methods of data collection, statistical analysis, and the summary.
Population
The population selected for this study was out of hospital drug boxes located on
ambulances and rescue trucks in the Verde Valley are of Arizona. These drug boxes are
located on the equipment of three different agencies: Sedona Fire District, Verde Valley
Fire District, and Verde Valley Ambulance Company. the response areas of these
companies cover the entire Verde Valley area. This is useful as it allows for the widest
All three of these agencies maintain their equipment in heated/cooled garages
except when out on an EMS assignment. None of the equipment is stored in the open
without protection or has any temperature control devices in place at the present time. In
addition, all the agencies use either a Plano or Pelican brand drug box for storage of their
Research Variables
This study centers around the minimum and maximum temperatures reached in
the out of hospital drug boxes in the Verde Valley. The control variable was the
temperatures reached in the drug boxes without any temperature control devices or
interventions. The interventions consisted of additions of solid foam insulation to the
drug box compartments. The goal of the study was to compare the temperatures of the
drug boxes with and without insulation. The two sets of temperatures will be assessed for
compliance with the acceptable temperature range of 46º - 86º F.
Field Procedures
Reading of the temperature ranges were done by the on duty crew at each of the
fire/EMS stations. The temperatures were recorded for the first response ambulance or
rescue truck for each agency for a total of three vehicles. Readings took place every third
day and the results were collected by the principle investigator. The results were
Methods of Collection
Data were collected by placing a minimum/maximum thermometer n each of the
designated drug boxes. The temperatures were read every third day for three weeks,
consistent with an A-B-C shift rotation. The temperatures were read when the duty crew
was doing mandatory drug box checks. Additional data were gathered in the same
manner from the same drug boxes after modifications were made. Modifications
consisted of rigid foam insulation readily available at a local home improvement center.
Statistical Analysis
A t-test design was used to determine if there was a significant difference between
the two sample means. The first sample was the control group using no means of
temperature control in the drug boxes. The second sample was the experimental group
using solid foam insulations in the drug box compartments.
In this chapter the research variables for the control and experimental groups were
defined. The characteristics of the chosen population were outlined along with a
discussion of field procedures and methods of collection. Chapter IV discusses the
findings of the study and data analysis.
CHAPTER IV FINDINGS
This chapter presents the findings of this study. The research hypothesis will be discussed
in relation to temperature ranges and variations. The control group data provides a
baseline of temperature ranges, with the control group addressing the hypothesis. All
findings are correlated with the hypotheses stating the temperatures will remain in an
acceptable range when rigid insulating foam is used. In brief, the addition of the rigid
foam insulation did not contribute significantly to keeping drug box temperatures in an
acceptable range. Details of temperature ranges, averages, and statistical significance will
be covered in the data collection results.
Data Collection Results
Verde Valley Fire District was the first agency chosen to carry a min/max
thermometer in its drug box compartment. Data were gathered in compliance with the
stated methods of collection. The maximum temperature in the control data was 68º F.,
the minimum was 40º F., and the average was 54º F. The maximum temperature for the
experimental data was 73º F, the minimum was 40º F and the average was 53.5º F.
Figures 1 and 2 show the complete sets of data for the control and experimental groups
respectively. Results are presented in graphical form for ease of visualization.
Figure 1 - VVFD Figure 2 -VVFD
The second agency is Verde Valley Ambulance Company. The drug compartment
control temperatures for this agency ranged from a low of 44º F. to a high of 80º F. The
average temperature was 60º F. Temperatures from the control data ranged from a low of
44º F to a high of 72º F, with an average of 57º F. Figures 3 and 4 show the complete sets
Figure 3 - Verde Valley Ambulance Figure 4 - Verde Valley Ambulance
The third and final agency that carried a min/max thermometer in its drug box was
Sedona fire District. This agency is at the highest elevation of the three and houses it’s
engines and ambulances in a heated bay. The temperatures for the control data ranged
from a low of 53º F. to a high of 84º F. with an average of 68º F. The full set of data for
control and experimental groups are shown in figures 5 and 6 respectively.
Figure 5 - Sedona Fire District Figure 6 - Sedona Fire District
It is of interest to note that while each grouping of data shows variation within its own
temperature ranges there is very little overlap in temperature ranges between the three
agencies. This shows the need for much individualization of planning as data from one
elevation or geographical area do not easily or accurately transfer to others. Figure 7
attempts to demonstrate this stratification of maximum control temperature ranges for all
three agencies. See figure 8 for control minimum ranges, figure 9 for experimental
maximums and figure 10 for experimental minimums.
Figure 7 - Maximum control ranges Figure 8 - Minimum control ranges Figure 9 - Maximum experimental ranges Figure 10 - Minimum experimental ranges Statistical Analysis of the Data
A t-test design was used to determine if there was statistical significance between the
temperature ranges of the control group and the experimental group. A total of 3 t-tests
were performed. The first was on the maximum temperatures, the second on the
minimums, and the third on the daily average temperatures. A software formula available
on the internet was used to perform the t-test computations (Student’s t-test). The results
¾ For the maximum temperatures the t = 0.495 with a standard deviation of 6.71
¾ For the minimum temperatures the t = 1.19 with a standard deviation of 6.45 and
¾ For the average daily temperatures the t = 0.882 with a standard deviation of 6.30
Using the t-test tables for a one-tailed test the level of significance at the 0.05 level is
Using this data the study must reject the initial hypothesis that stated use of a foam
insulator would keep drug temperatures within an acceptable range. For this study the
significance is that using solid foam insulation alone as will not reliably keep the drug
box temperature between the recommended 46º to 86º F. range.
The data collected for this study has shown the temperature variations for both
un-insulated and insulated drug boxes. It has shown that each agency has a very specific
temperature range that does not overlap the ranges of the other agencies, but does show
consistency of storage within each agency.
Analysis of the data has shown that using a solid foam insulator alone does not
significantly impact temperature swings enough to reliably keep the drug boxes within
CHAPTER V SUMMARY, CONCLUSIONS, AND RECOMMENDATIONS
The purpose of this study was to determine the effect solid foam insulation had on
the temperature variations in prehospital drug boxes during the months of October and
November 2006. Specifically if the insulation would keep the drug boxes within the
recommended temperature range of 46º to 86º F. The study was prompted by indications
from ADHS that temperature controls for drug boxes would soon be required in all
prehospital drug boxes. The hypothesis: drug box temperatures will remain within an
acceptable range when insulated with solid foam was used to guide the direction of this
study. Three agencies in the Verde Valley allowed min/max thermometers to be placed in
their drug boxes. One agency, Verde Valley Ambulance was based within the city limits;
the second Verde Valley Fire in the suburban foothills; and the third, Sedona Fire in Oak
Creek Canyon. Min/max temperatures were collected every three days at approximately
9am from the drug box compartments that had no insulation. Then additional data were
gathered from the same drug boxes after 2” solid foam insulation was added to the drug
box compartments. Min/max temperatures were again gathered and then compared to the
Conclusions
The conclusions of this study are based on the hypothesis that states use of solid
foam insulation in the drug box compartments will keep the drug boxes within an
acceptable temperature range. This temperature range was based on recommendations
The t-test values obtained from this study indicate that this hypothesis can not be
upheld. All t-values were below the 0.05 level of significance for a one tailed t-test. This
can be interpreted to mean that the addition of solid foam insulation to the drug box
compartments did not make significant difference in the maintenance of the required
range of temperatures. This study indicates that the original hypothesis must be rejected.
Recommendations
The data collected for this study were done during the months of October and
November 2006. In order to make decisions for year round storage, further studies are
recommended that cover temperature variations for an entire calendar year. This would
make available data from all seasonal temperature extremes for this area.
In retrospect, this author feels that future studies should include daily min/max air
temperature for the Verde Valley area in addition t the actual drug box temperatures. this
would allow for a correlation between variations in air temperatures, weather patterns,
and drug box temperatures. A future study might build on this data by including a
commercial storage product and a product such as frozen blue ice to the experimental
variables for comparison with the sold foam insulation data.
Finally, a study of the cost of adding a commercial unit to each ambulance
compared to the yearly cost of drug replacement due to temperature swings might help
clarify the usefulness of the commercial unit and put their costs into perspective.
Allegra, J.R., Brennan, J., Lanier, V., Lavery, R., & MacKenzie, B. (1999). Storage
Temperatures of Out of Hospital Medications. Academic Emergency Medicine.
Arizona Department of Health Services, Bureau of Emergency Medical Services. (2005).
R9-25-101 Working Draft Revision 4. Retrieved June 1, 2006 from
Biomedical Equipment & Engineering Services Company. (2006). PharmGuard.
Bowman, L. (2004). Study: shipping through mail can degrade medicine. Scripts Howard
News Service). Retrieved June 22, 2006 from
Brown, L.H. & Campagna, J.D. (2005). Medication storage in the EMS environment:
understanding the science and meeting the standards. Emergency Medical
Brown, L.H., Krumperman, K., & Fullagar, C.J. (2004). Out of hospital medication
storage temperatures: a review of the literature and directions for the future.
Prehospital Emergency Care. v.8, April-June 2004, 200-206.
Brown, L., Wojcik, S., Bailey, L., & Tran, C. (2004). Medications storage temperatures
on U.S. ambulances: exposures of varying durations and the effects of a simple
stock rotation scheme. Prehospital Emergency Care. v.8, 83.
Church, W.H., Hu, S.S., & Henry, A.J. (1994). Thermal degradation of inject able
American Journal of Emergency Medicine. v. 12, 206-309.
Engel Corporation. (2006). SteadyTemp. Retrieved July 11, 2006 from
Gottenwald, M.D., Akers, L.C., Liu, & PK et al. (1994). Prehospital stability of
diazepam and lorazepam. American Journal of Emergency Medicine. v. 17, 333-
Grant, T.A., Carroll, R.G., Church, W.H. et al. (1994). Environmental temperature
degradation in epinephrine concentrations and biologic
American Journal of Emergency Medicine. v.12, 319-322.
Helm, M., Castner, T., & Lampl, L. (2003). Environmental temperature stress on drugs
in prehospital emergency medical services. Acta Anaesthesiologic Scandinavica.
Johansen, R.B., Schafer, N.C., & Brown, P.I. (1993). Effects of extreme temperatures on
drugs for prehospital ACLS. American Journal of Emergency Medicine. v. 11,
Mermaid Manufacturing. MK747: Medi-Kool Unit. (2006). Retrieved June 22, 2006
Mehta, S.H., Doran, J.V. Lavery, R.F. & Allegra, J.R., (2002) Improvements in
prehospital medication storage practices in response to research. Prehospital
Palmer, R.G., Zimmerman, J., Brown, P.C., & Clawson, J.J. (1985). Altered states:
the influence of temperature on prehospital drugs. Journal of Emergency Medical
Pharmacopeial Forum. (2006, June). Emergency Medical Services Vehicles and Ambulance-Storage of Preparations. In process revision. U.S. Pharmacopeia
12501 Twinbrook Parkway, Rockville, MD 20852.
Students t-test. Retrieved November 20, 2006 from
Thermal Engineering Branch Website. (2004). Thermally stabilized paramedic drug box for fire trucks. Retrieved June 7, 2006 from
The United States Pharmacopeial Convention, Inc. (2005). Toronto, Ontario: WebCom
Virginia Beach Department of Emergency Medical Services. (2005). Medication storage
INCREMENTO PATRIMONIAL NO JUSTIFICADO Y LOS FONDOS DE ORIGEN ILÍCITO: ¿PRESUNCIÓN O FICCIÓN? 1. Introducción Según lo dispone el primer párrafo del artículo 52º de la Ley del Impuesto a la Renta aplicable en el Perú, se presume que los incrementos patrimoniales cuyo origen no pueda ser justificado por el deudortributario, constituyen renta neta no declarada por éste. Se añ
DON ÁLVARO DE LUNA TRAGEDIA EN CUATRO ACTOS Por Santiago Sevilla Larrea INTRODUCCIÓN Las coplas del insigne poeta Don Jorge Manrique, coetáneo de los Reyes Católicos, nos plantean ciertas preguntas filosóficas que han quedado hasta ahora, por más de quinientos años, sin una respuesta dramática: “¿Qué se hizo el rey don Juan? Los Infantes de Aragón, ¿qué se hicieron? ¿q