Ramanathan R, Siassi B, deLemos R A
Department of Pediatrics, Hospital of The Good Samaritan, University of Southern California School of Medicine, Los Angeles, USA.
J Perinatol. 1995 May-Jun;15(3):178-82; quiz 183-4.
With advances in neonatal intensive care survival of extremely low birth weight (< 1 kg) infants has increased significantly over the past decade. Dexamethasone is used increasingly for the prevention and treatment of chronic lung disease in these infants. The impact of dexamethasone therapy on the incidence or severity of retinopathy of prematurity (ROP) remains controversial. We conducted a retrospective study to evaluate the association between short-term dexamethasone treatment and severe ROP in extremely low birth weight infants. From October 1989 to December 1992, 309 very low birth weight infants were admitted to the neonatal intensive care unit. A total of 266 infants (86%) survived until hospital discharge. Of these, 90 weighed less than 1 kg. Thirty-eight of 90 infants received short-term dexamethasone therapy for chronic lung disease and the remaining 52 infants did not. Infants treated with dexamethasone and those not treated with dexamethasone were comparable in birth weight (820 vs 828 gm), gestational age (26.5 vs 26.9 weeks), inborn (11 vs 14), and occurrence of sepsis (13/38 vs 21/52). Infants treated with dexamethasone required longer periods of mechanical ventilation (44 +/- 23 vs 26 +/- 15 days, p < 0.001), had longer duration of supplemental oxygen (57 +/- 28 vs 29 +/- 23 days, p < 0.001), had higher incidence of patent ductus arteriosus (28/38 vs 18/52, p < 0.0003), and required surfactant therapy more often for respiratory distress syndrome (17/38 vs 11/52, p < 0.01), when compared with infants who did not receive dexamethasone. Severe ROP developed in 16 infants (stage III or higher); 12 of these were in the dexamethasone-treated group (p < 0.003). Thirteen infants required cryotherapy; nine were from the dexamethasone-treated group (p < 0.13). This study demonstrates an apparent association between the incidence of severe ROP and dexamethasone therapy. Prospective, randomized, controlled studies are needed to correct for differences in severity of cardiorespiratory illness to establish whether a causal role exists for steroid therapy in ROP. Until such studies are available, careful consideration must be given to indications, dosage, time of initiation, and duration of treatment with dexamethasone in extremely low birth weight infants.
在过去十年中,随着新生儿重症监护技术的进步,极低出生体重(<1千克)婴儿的存活率显著提高。地塞米松越来越多地用于预防和治疗这些婴儿的慢性肺病。地塞米松治疗对早产儿视网膜病变(ROP)的发生率或严重程度的影响仍存在争议。我们进行了一项回顾性研究,以评估短期地塞米松治疗与极低出生体重婴儿严重ROP之间的关联。从1989年10月至1992年12月,309名极低出生体重婴儿被收治入新生儿重症监护病房。共有266名婴儿(86%)存活至出院。其中,90名婴儿体重不足1千克。90名婴儿中有38名接受了地塞米松短期治疗以治疗慢性肺病,其余52名婴儿未接受治疗。接受地塞米松治疗的婴儿与未接受地塞米松治疗的婴儿在出生体重(820克对828克)、胎龄(26.5周对26.9周)、是否为足月儿(11对14)以及败血症发生率(13/38对21/52)方面具有可比性。与未接受地塞米松治疗的婴儿相比,接受地塞米松治疗的婴儿需要更长时间的机械通气(44±23天对26±15天,p<0.001),吸氧时间更长(57±