PEDIATRICS Vol. 100 No. 2 August 1997,
p. e9
Copyright ©1997 by the American Academy of Pediatrics
ELECTRONIC ARTICLE:
Evolution in the Recognition of Infantile Hypertrophic Pyloric
Stenosis
Frieda Hulka
,
Timothy J. Campbell§,
John R. Campbell*, and
Marvin W. Harrison*
From the * Division of Pediatric Surgery, the
Department of
Surgery, School of Medicine, Oregon Health Sciences University, and
§ Emanuel Hospital, Portland, Oregon.
ABSTRACT
INTRODUCTION
PATIENTS AND METHODS
RESULTS
DISCUSSION
ABBREVIATIONS
REFERENCES
ABSTRACT
Purpose. To analyze changes in the
clinical condition at presentation and methods of establishing the
diagnosis of infantile hypertrophic pyloric stenosis (IHPS).
Methods. Retrospective review of patients who underwent
pyloromyotomy (PM) for suspected IHPS at two institutions from 1969 through 1994 was performed. For the purposes of comparison, the population was divided into five equal time periods.
Results. Over the 25-year period, 901 infants
underwent PM. Patients presented at a younger age, weighed more, and
had a shorter length of illness in the most recent time period.
Hypochloremic alkalosis was found half as frequently in the most recent
time period compared to the earliest group. A palpable pyloric tumor was present in 79% of patients in the earliest time period compared with 23% in the most recent time period. Sixty-one percent of patients
in the earliest group and 96% in the latest group underwent an imaging
study, reflecting the referring physician's evaluation before referral
to the surgeon.
Conclusions. Currently, patients with IHPS less
frequently present with the clinical hallmarks of the disease. The use
of imaging studies to establish the diagnosis has become common
practice. The result has been the diagnosis of IHPS before alkalosis
has developed, a shorter clinical course, less morbidity, and a shorter postoperative hospital stay.
Key words:
pyloric stenosis,
pyloromyotomy,
diagnosis,
hypochloremic alkalosis,
upper gastrointestinal series,
abdominal ultrasonography.
INTRODUCTION
Traditionally, the diagnosis of infantile hypertrophic
pyloric stenosis (IHPS) is based on a history of projectile, nonbilious vomiting, and palpation of a pyloric tumor.1,2 The
presence of hypochloremic alkalosis has also been associated with
IHPS.3 Infants with historical but not physical findings
consistent with IHPS undergo radiologic evaluation by either upper
gastrointestinal series (UGI) or, more recently, abdominal ultrasound
(U/S) to establish the diagnosis. The increased reliance of radiologic tests to diagnose IHPS has been ascribed to inexperienced examiners not
palpating a pyloric tumor and subsequently proceeding with further
evaluation.4 To evaluate temporal trends in the
presentation and methods of diagnosis of IHPS, we performed a review of
patients who underwent pyloromyotomy (PM) in the past 25 years.
PATIENTS AND METHODS
A retrospective chart review of patients who underwent PM for
suspected IHPS at two teaching institutions between 1969 and 1994 was
performed. All patients were examined and subsequently operated on by
one of the authors (T.J.C., J.R.C., M.W.H.). Only patients with
confirmed IHPS at the time of surgery were included in this analysis.
Data included demographic information, history of illness, physical
findings, admission laboratory values, and results of any imaging study
performed. The preoperative and total length of stay were calculated in
hours from the dates and times of admission, operation, and discharge.
For the purposes of comparison, the study population was divided into
five groups representing 5-year increments. When appropriate, values
were expressed as a mean with standard deviation. All five groups were
compared using analysis of variance. Comparison of the earliest with
the most recent group was performed with the Student's t
test for continuous variables and the
2 test for
categorical variables. A P value of less than .05 was considered statistically significant. All tests were performed using
the SPSS for Windows version 6.1 statistical program (SPSS Inc,
Chicago, IL).
RESULTS
Over the 25-year period, 901 infants underwent PM for IHPS.
Overall, 81% of patients were male infants. The mean age was 38 days
(range 0 to 171 days) and the mean weight was 3934 g (range 2040 to 6840 g). A family history of pyloric stenosis was found in 12%
of patients. Prematurity was present in 4% of patients. Congenital
anomalies were found in 11% of patients. Only 1 infant underwent a
negative exploration.
Analysis of the five time periods demonstrated that patients presented
at a younger age, weighed more, and had a shorter length of illness in
the most recent interval (Table 1). The prevalence of
prematurity and positive family history of pyloric stenosis did not
vary over time. The frequency of palpation of a pyloric tumor by the
pediatric surgical staff decreased significantly over time
(P < .001).
|
Table 1.
Demographic and Physical Characteristics
[View Table]
|
Electrolytes including sodium, potassium, and chloride were assessed at
the time of admission in 98% of patients. Blood gas analysis was
obtained in 10% of patients. Serum bicarbonate was added to the
standard electrolyte panel in 1981 at one hospital and 1983 at the
second hospital; therefore, analysis including bicarbonate is limited
to the later half of the study. Metabolic derangements at admission
were found less frequently over time (Table 2).
Hypochloremia (defined as a serum chloride of less than 90 mEq/L) or
alkalosis (defined as a pH of greater than 7.46) decreased in frequency
in the later years (Fig 1).
Fig. 1.
The proportion of infants in each time period with hypochloremia, Cl
<90 mEq/L and alkalosis, pH >7.46.
[View Larger Version of this Image (25K GIF file)]
An imaging study, either an UGI or abdominal U/S was performed in 90%
of the entire study population. Eighty percent of these tests were
ordered by the referring physician, not by the pediatric surgeon. UGI
was used exclusively until 1983 when U/S was introduced to both
hospitals as an alternative diagnostic test in patients with suspected
IHPS. One imaging study was performed in 61% of patients in the
earliest time period compared with 96% in the most recent time period
(Fig 2). Diagnostic imaging was ordered by the referring
physician increasingly over time, ranging from 74% in the earliest
time period to 86% in the most recent time period.
Fig. 2.
The proportion of infants who had diagnostic studies in each time
period. The use of UGI declined as U/S was more commonly utilized. Both
UGI and U/S in combination have become common. Less than 10% of
infants had only physical examination as the sole diagnostic study.
[View Larger Version of this Image (27K GIF file)]
Preoperative length of stay (PLOS) varied throughout the study
(Fig 3). The PLOS was initially greater than 1 day; however, it declined to .68 days during the middle portion of the study period.
An increase in the PLOS to greater than 1 day was found again in the
most recent time frame. The total length of stay (TLOS) initially
declined then remained stable.
Fig. 3.
Length of stay for infants with IHPS has changed little since the
1975-1979 period. The preoperative length of stay increased as UGI and
U/S were used more frequently.
[View Larger Version of this Image (23K GIF file)]
DISCUSSION
The clinical hallmarks of IHPS include a male infant between 2 and
3 weeks of age with nonbilious, projectile vomiting.3 In the past, a palpable pyloric tumor was detected in 70% to 90% of
patients with IHPS.1,2,7 Persistent vomiting of gastric contents can lead to the development of dehydration and hypochloremic alkalosis. The number of infants with IHPS and marked electrolyte abnormalities requiring treatment varies from 13% to 25% in several series.11 The degree of electrolyte abnormalities has
been associated with the length of illness.12
This analysis demonstrates that the aforementioned classical features
of IHPS have decreased in frequency over time. The length of illness
before admission declined during this study. Weight loss, dehydration,
and metabolic abnormalities became less common. Physical examination
yielded positive findings in only 23% of infants in the last 5 years
of inquiry compared with 79% in the first 5 years. Presumably,
palpating a pyloric tumor in healthier, less emaciated, vigorous
infants was more difficult, decreasing the sensitivity of the physical
examination. Macdessi5 also found a significant decline in
palpable pyloric tumors over time, but an association with duration of
illness was not established.
Imaging studies were routinely used to diagnose IHPS in the last
10 years of this study. Studies published before 1975 reported between
8% and 38% of infants with IHPS undergoing radiologic evaluation
before surgical intervention.1,2,7,16 However, diagnostic imaging was utilized increasingly in more recent
series.5,6
The referring physician ordered the majority of diagnostic tests
performed before referral. Others have demonstrated a similar pattern.6,9,14 Presumably, a pyloric tumor was not palpated by the referring physician and this prompted further evaluation of
the patient's vomiting. Increased usage of imaging modalities to
diagnose IHPS has raised the concern that physical examinations by
inexperienced physicians has lead to the performance of unnecessary tests.4,19,20 During the earlier periods of this study,
72% of UGIs ordered by referring physicians subsequently had a pyloric tumor palpated by the pediatric surgeon. However, in the last 5 years
of study, only 21% of imaging studies ordered by referring physicians
were performed in infants with a palpable pyloric tumor. As palpable
pyloric tumors became less frequent, an imaging study was necessary for
diagnosis.
PLOS is an indicator of the patient's clinical status. It can also be
a measure of the uncertainty of the diagnosis. In the earlier years,
when patients presented more frequently with metabolic derangements, rehydration and electrolyte replacement were more often
necessary before surgery. PLOS decreased during the middle period of
the review. However, over the last 10 years, PLOS increased again
correlating with the more routine use of imaging studies and the time
required to perform one or more imaging studies for diagnosis. An
increase in PLOS and diagnostic studies being performed have coincided
with these changes in the presentation and diagnosis of infants with
IHPS. Nevertheless, the TLOS decreased over the study period.
One question this study raises is why the change in presentation of
IHPS over time? This study demonstrates that over time, infants were
not as ill when they presented. The most probable reason for this is
the earlier usage of imaging studies in an outpatient setting to ensure
the diagnosis of IHPS. Infants were diagnosed with IHPS before they had
significant metabolic abnormalities, weight loss, or the pathonomonic
finding of a pyloric tumor.
Is the early use of an imaging study necessary? Is it more
cost-effective to obtain an UGI or U/S in an infant who has been vomiting for a few days to rule out IHPS or risk the infant becoming dehydrated from persistent vomiting and require hospitalization for
electrolyte abnormalities? If we use PLOS as an indicator of the
patient's clinical status to determine the cost of hospitalization for
dehydration, an estimated .52 days are needed to correct metabolic abnormalities. (This calculation reflects the difference between the
PLOS during the earliest time period of this study [1.2 days] when
more patients had metabolic derangements, and the middle portion of the
study [.68 days] when fewer metabolic derangements were encountered).
The current charge of an UGI or U/S at our hospitals is less than a
half-day of hospitalization.
We recommend the following algorithm to diagnose IHPS: when an infant
presents with vomiting, attempts to palpate a pyloric tumor should be
made. If the primary physician is unable to palpate a pyloric tumor but
has a high index of suspicion, a pediatric surgeon should examine the
patient. If a pyloric tumor is palpated, the patient should undergo PM.
If no tumor is palpated or a pediatric surgeon is not available, an
imaging study should be performed.
FOOTNOTES
Received for publication Feb 5, 1997; accepted Mar 24, 1997.
Reprint requests to (J.R.C.) Division of Pediatric
Surgery
L223, Oregon Health Sciences University, 3181 SW Sam Jackson
Park Rd, Portland, OR 97201.
ABBREVIATIONS
IHPS, infantile hypertrophic pyloric stenosis.
UGI, upper gastrointestinal series.
U/S, ultrasound.
PM, pyloromyotomy.
PLOS, preoperative length of stay.
TLOS, total length of stay.
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