Archives of Environmental Health
May/June 1991 (Volume 46, Issue 3; Pages 155-160.)
Acute Health Effects in a Community After a Release of Hydrofluoric
Acid
JESSIE S. WING, M.D.*
LEE M. SANDERSON, Ph.D.*
Office of Surveillance and Analysis
Center for Chronic Disease Prevention
and Health Promotion
Centers for Disease Control
Atlanta, Georgia
JEAN D. BRENDER, Ph.D.
DENNIS M. PERROTTA, Ph.D.
RICHARD A. BEAUCHAMP, M.D.
Epidemiology Division
Texas Department of Health
Austin, Texas
*Drs. Wing and Sanderson were formerly with the
Center for Environmental Health and Injury Control, Environmental
Hazards and Health Effects Division, Centers for Disease Control,
Atlanta, Georgia.
ABSTRACT. Approximately 3 000 persons
were evacuated from a Texas community
after 24 036 kg (53 000 lb) of caustic hydrofluoric acid (HF)
were released from a nearby petrochemical plant. Emergency room
and hospital records of 939 persons who were seen at two area
hospitals were reviewed. Most persons who presented at the emergency
rooms were female (56%) or black (60%), and their mean age was
33.9 y. The most frequently reported symptoms were eye irritation
(41.5%), burning throat (21 %), headache (20.6%), and shortness
of breath (19.4%). Physical examination results were normal for
49% of the cases; however, irritation of the eyes, nose, throat,
skin, and lungs were noted on other exams. Decreased pulmonary
function was demonstrated by pulmonary function tests (forced
expiratory volume in the first second, < 80% of predicted value,
42.3%); hypoxemia (pO2 < 80 mm Hg, 17.4%) and hypocalcemia
(< 8.5 mg/dI, 16.3%) were also noted. Ninety-four (10%) of
the cases were hospitalized, and more than 83% of all cases were
discharged with a primary diagnosis of "HF exposure." There are
several reports of individuals who are acutely and chronically
exposed to HF; however, we are unaware of other published reports
that describe exposure of a community to HF. This incident represented
a unique opportunity to study the immediate health impact on a
community of residents who were exposed to a hazardous materials
release. Results of this analysis suggest that (a) initial health
problems should be followed up, (b) any long-term health effects
of HF exposure must be assessed, and (c) the health impact on
the population at risk should be determined.
HYDROFLUORIC ACID (HF) is a caustic, industrial
compound used in the production of high-octane gasoline, aerosols,
plastics, and refrigerants. It has been used in glass etching since
the seventeenth century. (1)
In October 1987, a release of HF occurred at a
petrochemical plant in Texas. Two pipes on a storage tank that contained
isobutane-saturated HF were sheared during maintenance operations,
and gas spewed from the tanks. Within 7 min of the release, a water
curtain was established to contain and rehydrate escaping gas. Nonetheless,
at approximately 5:20 P.M. on the night of the local homecoming
celebration, a vapor cloud drifted across a community of 41 000
residents. Approximately 24 036 kg (53 000 lb) of anhydrous HF and
2 993 kg (6 600 lb) of isobutane were ventilated during a 48-h period.
Within 20 min of the release, persons within .8 km (.5 mi) of the
plant were evacuated. Eventually, 3 000 individuals were evacuated
from an 8 km2 (5 mi2) area.
Methods
Representatives of the Texas Department of Health
and the Centers for Disease Control visited the area 19 d after
the HF release to review the medical records of 939 persons who
reported being exposed to the chemical release.
The objectives of our study were to (a) describe
the medical characteristics of the 939 cases and (b) to compare
cases who were hospitalized with those who were treated and released
from the emergency rooms (ERs). We defined a case as a person who,
within 24 d following the HF release, came to hospital A or B and
expressed concern about HF exposure, or whose medical records contained
information regarding symptoms, signs, or diagnoses suggestive of
HF exposure.
We completed an abstraction form for the 94 cases
who were hospitalized at hospital A or B. Demographic information,
presenting symptoms and signs, medical history, results of physical
examination and laboratory tests, treatment, and discharge diagnoses
were recorded. We used a modified form to abstract information for
the 845 cases who were not hospitalized and who were treated and
released from either of the two ERs. All data were transferred to
dBase III files, which were then analyzed with the Statistical Analytical
System. In these analyses, only data obtained from a person's first
hospitalization or ER visit were included. (Thirty-four persons
visited the ER multiple times, and 5 were hospitalized more than
once.)
Results
The petrochemical plant is located in the southeastern
area of the community and is .4 km (.25 mi) from residential areas.
Most of the HF was ventilated during the first 2 hr of the release
in a low-lying plume across the city in a southeast to a northwest
direction.
Samples taken downwind 1 h after the release contained
10 ppm HF; and minimal traces of HF were found in samples obtained
2 h after the release. The following day, vegetation and exterior
surfaces located within 3.2 km (2 mi) northwest of the plant were
damaged; i.e., foliage was brown, car windows were etched, and car
paint was streaked. (2)
Hospital A, the smaller of the two hospitals in
our study, is located 2.4 km (1.5 mi) from the plant. It was visited
by 67.4% of all the cases. This hospital (a 120-bed facility) instituted
a disaster plan on the night of the release to reinforce its medical
staff and supplies. "Disaster tags" were provided to the first 231
cases (after which supplies were exhausted) who presented to Hospital
A. Location and activity of a case at the presumed time of exposure
to HF were obtained from information recorded on the disaster tags.
Cases who were hospitalized were generally older
than nonhospitalized cases (Table 1, mean age 41.5 y versus 33.1
y, respectively), We compared the cases with the 1980 U.S. Census
results for the city, and we found that more blacks (2-fold increase),
females (1.3-fold increase), and older persons (median age 33.9
y versus 28.9 y) were represented in our study.
| Table
1. - Characteristics of Nonhospitalized and Hospitalized Cases
Who Were Exposed to Hydrofluoric Acid Release |
| |
|
|
|
|
|
|
|
| Characteristic |
|
Nonhospitalized |
Hospitalized |
Total |
| Age |
|
|
|
|
Mean (y) |
|
33.1 |
41.5 |
33.9 |
Range |
|
33.1 |
5-79 |
<1-92 |
n |
|
832 |
94 |
926 |
| |
|
|
|
|
|
|
|
| |
|
No./n* |
(%) |
No./n |
(%) |
No./n |
(%) |
| Gender |
|
|
|
|
|
|
|
Female |
|
474/841 |
(56.4) |
52/94 |
(55.3) |
526/935 |
(56.3) |
Male |
|
367/841 |
(43.6) |
42/94 |
(44.7) |
409/935 |
(43.7) |
| Race/ethnicity |
|
|
|
|
|
|
|
White |
|
192/780 |
(24.6) |
28/94 |
(29.8) |
220/874 |
(25.2) |
Black |
|
472/780 |
(60.5) |
52/94 |
(55.3) |
524/874 |
(60.0) |
Hispanic |
|
115/780 |
(14.7) |
13/94 |
(13.8) |
128/874 |
(14.6) |
Other |
|
1/780 |
(0.1) |
1/94 |
(1.1) |
2/874 |
(0.2) |
| |
|
|
|
|
|
|
|
| *n = number for
whom data were available. |
The range of time
during which cases presented to the ERs after HF exposure is presented
in Figure 1. On the day of the release
(day 1), 44% of cases who presented to the ERs were hospitalized;
thereafter, the proportion of cases who were hospitalized decreased.
However, most cases who were not hospitalized visited ERs on day
3 (27%) or day 4 (21 %).
The majority (82.7%) of cases who were given disaster
tags were not occupationally exposed at the time of the release;
they were either at their homes or in their neighborhoods. There
were 39 occupationally exposed cases (i.e., police personnel, plant
employees, evacuation personnel) who were identified by information
on their disaster tag; however, most (72%) were not hospitalized
during this visit.
Symptoms. Cases who were not hospitalized
and who had no medical complaints on presentation to the ER numbered
120 (14.2%), whereas only 1 (1.1 %) case who was hospitalized had
no complaints (p < .001). Most of these nonhospitalized cases
who voiced no complaints presented to the ERs either on day 1 (n
= 60, 7%) or day 4 (n = 22, 2.6%) of the episode.
The symptoms reported most frequently among all
cases were eye irritation, throat burning, headache, shortness of
breath, and throat soreness (Table 2). Hospitalized cases reported
more headache (p < .05), shortness of breath, cough, nausea,
vomiting, dizziness, and skin burning than did nonhospitalized cases
(p < .001).
| Table
2. - Symptoms Reported by Nonhospitalized and Hospitalized
Cases Who Were Exposed to Hydrofluoric Acid Release |
| Symptom |
Nonhospitalized
(n = 845) |
Hospitalized
(n = 94) |
Total
(n = 939) |
| No. |
(%) |
No. |
(%) |
No. |
(%) |
| Eye irritation |
353 |
(41.8) |
37 |
(39.4) |
390 |
(41.5) |
| Throat burning |
171 |
(20.2) |
26 |
(27.7) |
197 |
(21.0) |
| Headache |
166 |
(19.6) |
27 |
(28.7) * |
193 |
(20.6) |
| Shortness of breath |
131 |
(15.5) |
51 |
(54.3) |
182 |
(19.4) |
| Throat soreness |
142 |
(16.8) |
22 |
(23.4) |
164 |
(17.5) |
| Chest pain |
137 |
(16.2) |
22 |
(23.4) |
159 |
(16.9) |
| Cough |
120 |
(14.2) |
34 |
(36.2) |
154 |
(16.4) |
| Nausea |
116 |
(13.7) |
25 |
(26.6) |
141 |
(15.0) |
| Vomiting |
52 |
(6.2) |
15 |
(16.0) |
67 |
(7.1) |
| Dizziness |
42 |
(5.0) |
22 |
(23.4) |
64 |
(6.8) |
| Skin burning |
46 |
(5.4) |
13 |
(13.8) |
59 |
(6.3) |
| Rash |
21 |
(2.5) |
4 |
(4.3) |
25 |
(2.7) |
| |
|
|
|
|
|
|
| *p < 0.5
p < .001 |
Physical examination.
Physical examination results were normal for 49% of the cases; however,
conjunctival and oropharyngeal irritation, pulmonary findings (i.e.,
rhonchi, rales, wheezing, or stridor), and dermal irritation (i.e.,
skin blisters, rash) were noted during other exams (Table 3). Erythema
was relatively frequent (including erythematous tonsils, n = 7).
There were also other cases with papules, tracheal ulcers, a hypertensive
episode (240/120 mm Hg), hyperventilation, and interuterine pregnancy.
Pulmonary function tests. Forced expiratory
volume in 1 s (FEV1.0) was less than 80% of the predicted values
for 30.2% and 53.7% of the nonhospitalized and hospitalized cases,
respectively (p = .01) (Table 4). The ratio of FEV1.0 to forced
vital capacity (FVQ was low for 3.2% of the nonhospitalized cases
compared with 29.9% of hospitalized cases (p < .001).
When stratified by exposure type, although only
10 of the occupationally exposed cases performed pulmonary function
tests, results for 70% (n = 7) were in the < 80% predicted range
compared with 40% (n = 48) who were not occupationally exposed.
Other laboratory results. The criteria employed
for obtaining and analyzing laboratory specimens were unclear, especially
for cases who were not hospitalized. Arterial blood gas (ABG) determinations,
which were made for 155 cases, revealed that 17.4% were hypoxemic
(pO2 < 80 mm Hg). More hospitalized cases (24%) experienced alkalotic
pH levels (pH 7.46-7.62) than did nonhospitalized cases (10%, p
< .001).
Discharge diagnoses. Eighty-three percent
of nonhospitalized cases had a primary ER diagnosis that was related
to HF exposure, compared with 94% of the hospitalized cases. Other
diagnoses among the hospitalized cases included asthma/bronchospasm,
bronchitis, respiratory distress, congestive heart failure/pulmonary
edema, pneumonia, tracheobronchitis, atelectasis, and esophagogastritis.
More than half of these cases were hospitalized for 1 d or less
(range < 1-12 d).
| Table
3. - Results of Physical Examinations for NonHospitalized
and Hospitalized Cases Who Were Exposed to Hydrofluoric
Acid Release |
| Finding |
Nonhospitalized
(n = 845) |
Hospitalized
(n = 94) |
Total
(n = 939) |
| No. |
(%) |
No. |
(%) |
No. |
(%) |
| Normal exam |
451 |
(53.4) |
10 |
(10.6)* |
461 |
(49.1) |
| Conjunctival irritation |
81 |
(9.6) |
10 |
(10.6) |
91 |
(9.7) |
| Pharyngeal irritation |
50 |
(5.9) |
5 |
(5.3) |
55 |
(5.9) |
| Pulmonary findings |
33 |
(3.9) |
18 |
(19.1)* |
51 |
(5.4) |
| Dermatologic findings |
33 |
(3.9) |
3 |
(3.2) |
36 |
(3.8) |
| Nasal irritation |
10 |
(1.2) |
2 |
(2.1) |
12 |
(1.3) |
| |
|
|
|
|
|
|
| *p <
.001 |
| Table
4. - Laboratory Results Obtained for NonHospitalized and
Hospitalized Cases Who Were Exposed to Hydrofluoric Acid
Release |
| Laboratory
finding |
Nonhospitalized |
Hospitalized |
Total |
| No. |
(%) |
No. |
(%) |
No. |
(%) |
| Decreased FEV1.0
(< 80% predicted) |
19/63
|
(30.2)
|
36/67
|
(53.7)å
|
55/130
|
(42.3)
|
| Decreased FEV1.0/FVC
¥ |
2/63 |
(3.2) |
20/67 |
(29.9)// |
22/130 |
(16.9) |
| Hypoxemia (pO2 < 80
mm Hg) |
16/80 |
(20.0) |
11/75 |
(14.7) |
27/155 |
(17.4) |
| Hypocalcemia (<8.5
mg/dl) |
19/128 |
(14.8) |
16/87 |
(18.4) |
35/215 |
(16.3) |
| |
|
|
|
|
|
|
| *n
= number tested.
Forced expiratory volume in 1 s (FEV1.0)
¥ Ratio of FEV1.0 to forced vital capacity (FVC);
normal > 70%.
å p = .01
// p < .001 |
Discussion
Hydrofluoric acid, when present as an acid mist,
can extensively irritate the eyes and respiratory tract, which can
result in intense lacrimation, sore throat, cough, lower airway
inflammation, and possible pulmonary edema-an effect that can be
manifested several hours later. The compound can cause topical and
systemic toxicity, the signs of which may only be apparent 24 h
after initial contact. (4) Hydrofluoric acid can also penetrate
the skin and hydrolyze; subcutaneous tissue can be damaged and deep,
painful ulcerations may occur. (5-7) Acute toxicity may affect the
gastrointestinal tract (diarrhea), liver (direct hepatotoxicity),
and kidneys (acute renal failure). Metabolic changes may occur,
which are usually secondary to hypocalcernia, hypomagnesemia, and
their sequelae. (8) Systemic fluorosis, myocardial injury, and death
have been reported after severe HF burns. (9-11)
The differences in demographic characteristics
of our cases may have resulted from variations in geographic distribution
of housing in the city and proximity to industrial areas, differential
use of medical facilities, demographic changes since the 1980 Census,
(12,13) social and economic variations, true exposure and health
effect differences, or other artifacts. The local homecoming celebration,
which occurred on the same day as did the release, may have also
influenced community activity and exposure.
Most cases who came to the hospitals soon after
the release probably experienced airborne exposure and inhalation,
both of which would result from the HF "fog." The spectrum of symptoms
reported included the,expected complaints of irritation to the eyes,
nose, throat, and lungs.' Pulmonary findings were prominent, especially
among cases who were hospitalized. Complaints of headache, dizziness,
nausea, and vomiting were also expressed frequently. (5)
The initial arterial blood gas determinations revealed
that 17% of all cases tested were hypoxemic. Perhaps this represents
intrapulmonary shunting of blood after HF inhalation, a finding
that has been reported previously for persons who inhale other acid
fumes. (4) Intrapulmonary shunting and hypoxemia may have contributed
to symptoms of headache and dizziness reported by some of our cases.
An impressive number of hospitalized cases also had alkalosis (pH
to 7.62), but there was no strong association between alkalosis,
serum calcium levels, or tachypnea.
For many, FEV1.0 values were low. Perhaps this
is a health effect or a dose response for cases who were occupationally
exposed to the HF release. The FEV1.0 values, which were worse for
hospitalized cases, may be a predictor of hospitalization. Or, they
may have resulted from personnel technique, possible malfunctioning
spirometry equipment, testing of patients en masse in emergency
settings, or another artifact. (15,16)
One reported side effect of HF exposure is hypocalcemia.
Most patients tested were eucalcemic; however, 16.3% were mildly
hypocalcemic (7.5-8.4 mg/di). There was very limited information
available on fluoride levels among our cases. A urine fluoride level
(1.7 mg/1) reported for one hospitalized case was not elevated.
Urinary excretion of fluoride, which is determined easily and probably
reflects the amount of chemical absorbed, is used as an index of
fluoride exposure and has been related to osteofluorosis.(8, 14)
Historically, medical treatment for HF exposure
has varied.(3, 17-20). In our study, medical personnel at hospitals
A and B prescribed calcium gluconate or calcium chloride preparations
for ocular, dermal, respiratory, and intravenous therapy; supplemental
oxygen inhalation; and bronchodilator or steroid medications.
Fourteen percent of all nonhospitalized cases had
no complaints upon presentation to the ERs. The time of presentation
for the nonhospitalized cases was bimodal. These individuals may
represent those who were concerned about HF exposure immediately
after the release (day 1), those who presented on Monday (day 4,
after the evacuation period ended), or those "worried well" who
may have presented to the hospitals for other reasons.
There were anecdotal accounts of cases hospitalized
soon after the incident for purposes of observation (and hospitalization
periods were usually brief). At the time of the HF release, most
physicians' offices and clinics were closed. This record review
probably captured the most critically ill or the most extensively
exposed cases immediately after the release; a few cases, however,
may have been "lost" to medical centers in other communities.
This study also illustrates the pattern of health
care utilization by a community after a toxic exposure. The disparity
in time of presentation (Fig. 1) and
presenting symptoms and signs suggest that early findings, particulary
among hospitalized cases, may reflect airborne exposure to acid
mist that causes mucous membrane and respiratory irritation (i.e.,
conjunctival and oropharyngeal irritation, dyspnea). Cases who presented
later in the post-impact period may reflect continued HF exposure
and/or nontreatment and symptoms and signs (i.e., burning, itchy
skin, rashes) that may have occurred during the clean-up phase of
the episode (especially among nonhospitalized cases). Many cases
who were not hospitalized and who complained of skin rashes presented
on day 4 (n - 6, 29%) or day 6 (n - 5, 24%) of the episode.
The data have several limitations, including the
validity of self-reported historical information, incompleteness
or under-reporting of some variables, and treating patients en masse
in an emergency setting. The medical records from the hospitalized
cases may be more complete than those of nonhospitalized cases,
and the records may not necessarily reflect more health problems
in the hospitalized group. However, after a toxic chemical release,
more medical problems in a patient may also be a predictor of hospital
admission.
Further studies could be conducted to (1) follow
up cases for whom positive findings were noted (symptoms, physical
findings, or laboratory results), (2) obtain additional information
on occupationally exposed cases; (3) review pulmonary function test
data (including original spirometry plots), (4) map cases for whom
locations during exposure were known (home address may not be an
adequate proxy because many were exposed outside their homes), and
(5) consider an evaluation of the population at risk. Epidemiologic
and medical evaluations of individuals who were potentially exposed
but who did not present at these hospitals could be conducted to
determine the full extent of the impact and possibly to justify
the establishment of a registry for exposure and health effects.
The emergency response to this incident should be evaluated and
coordinated among industry, community, civil defense, hospitals,
and medical personnel, and methods to improve disaster preparedness
and treatment protocols should be addressed.
* * * * *
The authors thank Drs. Ralph Morris and Ed lbert,
Ms. Sue Broussard, Ms. Toni Harris, and staff at hospitals A and
B for their cooperation and support.
Submitted for publication March 21, 1990; revised;
accepted for publication December 27, 1990.
Requests for reprints should be sent to: J. S.
Wing, M.D., Office of Surveillance and Analysis, Center for Chronic
Disease Prevention and Health Promotion, Centers for Disease Control,
1600 Clifton Road, MS K-30, Atlanta, GA 30333.
* * * * *
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To learn more about fluoride air pollution,
see www.fluoridealert.org/f-pollution.htm
|