Académique Documents
Professionnel Documents
Culture Documents
Springer-Verlag 2002
ORIGINAL ARTICLE
Introduction
It is well-recognized that inguinal hernia (IH) is a
common developmental problem in infants and children.
It is more common in low-birth-weight (LBW, < 2,500
g BW) infants than in term neonates [8, 10]. The reported incidence ranges from 5% to 30% depending on
the BW [2, 4, 15, 17]. The incidence of IH increases with
decreasing BW and is highest in extremely LBW
(ELBW) infants as reported in earlier literature [9].
Patency of the processus vaginalis is the major factor
in the development of IH [19]. By 32 weeks gestation, the
testes in males have normally entered the scrotum and
contraction of the inguinal canal around the spermatic
cord has begun [14]. Presumably, contraction of the female inguinal canal and narrowing of the canal of Nuck
occur at a similar gestational age (GA) [14]. Testicular
descent and closure of the inguinal canal are not likely to
be completed as eectively if gestation is shortened or if
growth and development of the infant are hampered.
Prematurity is the single most important predisposing
factor for the development of IH [7]. Bronchopulmonary
dysplasia (BPD) has also been associated with an
148
Results
Incidence of IH by (GA) at birth
The overall incidence of IH in infants 32 weeks GA or
less, who were still in the unit at over 28 days of life was
9.34% (65/696). Figure 1 shows the incidence of IH in
149
150
Table 1 Study parameters in
Hernia and non-hernia groups
(NS not signicant, values
mean standard deviation,
P signicant at <0.05)
Variable
Hernia group
(n = 65)
Non-hernia group
(n = 65)
P value
26.66
943.27
57
26.98
41.97
60.12
102.09
113.54
9.93
26.60
930.98
54
20.97
32.22
44.68
76.87
91.43
10.45
NS a
NS a
NS b
NS a
< 0.02 a
< 0.02 a
< 0.01 a
< 0.003 a
NS a
a
b
2.17
272.42
(81.81%)
17.40
21.11
31.98
47.15
37.47
2.90
Discussion
The incidence of IH in full-term infants ranges from 1%
to 5% [10]. The estimated incidence in preterm infants
has ranged from 8% to 30% and has been found to vary
with BW, GA, and length of follow-up [2, 4, 15, 17].
Table 2 Incidence of inguinal
hernia in infants 1,500 g BW
literature review
2.41
346.58
(87.70%)
23.29
30.79
45.86
68.51
45.61
2.09
Author
Follow-up of infants
Incidence
in males
Incidence
in females
Incidence in
all infants
20 months corrected
age
6 months of age
13 years after birth
Primary hospitalization
26%
7%
16%
14%
NA
18.56%
2%
NA
2.9%
8.72%
18.90%
11.11%
151
nursery, and does not take into account the fact that
LBW infants, particularly boys, are at risk of developing
IH not only in infancy, but also up to 8 years of age and
beyond [12].
Among the risk factors studied, increased intra-abdominal pressure (IAP) is probably the most important
factor that predisposes to the development of IH
[16, 1820]. The fact that infants are predominantly
abdominal breathers makes it more likely that in the
presence of CLD, which increases IAP, an IH is more
likely to occur. The concentration and duration of
supplemental oxygen is a very good indicator of the
severity of CLD [1]. Of the measures of CLD in our
study, by regression model analysis only total oxygen
days were signicantly increased in infants with IH. The
length of hospital stay was signicantly longer in the
hernia group, which may in part be explained by the fact
that they had more severe lung disease (more days on
supplemental oxygen) and that they had to stay additional days for surgery and post-operative recovery.
Yeo and Gray reported that infants with respiratory
distress syndrome and those requiring mechanical ventilation were signicantly predisposed to the development of IH, especially males [27]. In another study,
bronchopulmonary dysplasia was associated with a
higher incidence of IH [11]. We have shown here that
factors associated with CLD such as days on mechanical
ventilation, CPAP, and supplemental oxygen were signicantly greater in infants who developed IH. We
therefore conclude that the severity of CLD plays an
important part in the development of IH in premature
infants.
In a study by Powell et al. [16], the best predictor
model gave a risk of IH that was inversely related to
BW, gender (M:F 11.5:1), intravenous feeding
(Y:N 3.1:1), and absence of respiratory distress
(Y:N 2.4:1), implying that the predominant predisposing factors for IH were nutritional rather than
respiratory, which is contrary to our ndings. We
studied weight gain expressed as g/kg-BW per day and
did not nd any dierence in weight gain in infants who
did or did not develop IHs. Although other factors
including feeding intolerance, gastroesophageal reux,
necrotizing enterocolotis, sepsis, total parental nutrition,
or caloric intake were not taken into account in this
study, we could still determine that ELBW infants with
IH did no worse than infants without IH with respect to
weight gain. We speculate that poor weight gain per se
may not increase the risk of IH, but factors that
contribute to failure to thrive (e.g., CLD, sepsis) may be
associated with IH by some other mechanism.
For infants in our study, surgery was performed
within 35 days of anticipated discharge from the unit
except when it was in response to a complication of the
hernia (incarceration, which occurred in only 1 infant).
By the time of surgery, all infants were on full enteric
nutrition and most of them were breathing room air.
Even though all of them required supplemental oxygen
during surgery, their postoperative oxygen require-
References
1. Bhutani VK, Abbasi S (1992) Long-term pulmonary consequences in survivors with bronchopulmonary dysplasia. Clin
Perinatol 19: 649671
2. Boocock GR, Todd PJ (1985) Inguinal IHs are common in
preterm infants. Arch Dis Child 60: 669670
152
3. Cote CJ, Zaslavsky A, Downes JJ, Kurth CD, Welborn LG,
Warner LO, Malviya SV (1995) Postoperative apnea in former
preterm infants after inguinal herniorrhaphy. A combined
analysis. Anesthesiology 82: 809822
4. Darlow BA, Dawson KP, Mogridge N (1987) Inguinal hernia
and low birthweight. N Z Med J 100: 492494
5. Georgie MK, Amarnath UM, Mills MM (1989) Determinants
of arm muscle and fat accretion during the rst postnatal
month in preterm newborn infants. J Pediatr Gastroenterol
Nutr 9: 219224
6. Gollin G, Bell C, Dubose R, Touloukian RJ, Seashore JH,
Hughes CW, Oh TH, Fleming J, O'Connor T (1993) Predictors
of postoperative respiratory complications in premature infants
after inguinal herniorrhaphy. J Pediatr Surg 28: 244247
7. Grosfeld JL (1989) Current concepts in inguinal hernia in
infants and children. World J Surg 13: 506515
8. Grosfeld JL (1989) Groin IH in infants and children. In: Nyhus
LM, Condon RE (eds) Hernia, Lippincott, Philadelphia, pp
8196
9. Harper RG, Garcia A, Sia C (1975) Inguinal hernia: a common
problem of premature infants weighing 1,000 grams or less at
birth. Pediatrics 56: 112115
10. Holder TM, Ashcraft KW (1980) Groin hernias and hydroceles. In: Textbook of Pediatric Surgery, Saunders, Philadelphia,
pp 594608
11. Hrabovsky EE, Sigmund WR, Mullett MK (1983) Inguinal
Hernia in the stressed premature infant. Perinatol Neonatol 7:
4551
12. Kitchen WH, Doyle LW, Ford GW (1991) Inguinal hernia in
very low birthweight children: a continuing risk to age 8 years.
J Paediatr Child Health 27: 300301
13. Matsuda T, Muguruma K, Hiura Y, Okuno H, Shichiri Y,
Yoshida O (1998) Seminal tract obstruction caused by childhood inguinal herniorrhaphy: results of microsurgical reanastomosis. J Urol 159: 837840
14. Moore KL (1977) Development of the inguinal canals. In: The
developing human. Saunders, Philadelphia, pp 239240,
253254
Reproduced with permission of the copyright owner. Further reproduction prohibited without permission.