The effect of pregnancy on kidney function in renal allograft recipients

JM Davison - Kidney International, 1985 - Elsevier
JM Davison
Kidney International, 1985Elsevier
The effect of pregnancy on kidney function in renal allograft recipients. In women with renal
transplants glomerular filtration rate (GFR) increases during pregnancy but how soon the
increment occurs, its relation to pre-pregnancy GFR, and the overall pattern of change are
unknown. Twenty-four hour creatinine clearances (24-hr Ccr) were measured prospectively
in ten pregnancies in eight allograft recipients before conception, throughout pregnancy, 8 to
12 weeks postpartum, and 4 to 6 monthly thereafter. Inulin (C1) and creatinine (Cr) clear …
The effect of pregnancy on kidney function in renal allograft recipients. In women with renal transplants glomerular filtration rate (GFR) increases during pregnancy but how soon the increment occurs, its relation to pre-pregnancy GFR, and the overall pattern of change are unknown. Twenty-four hour creatinine clearances (24-hr Ccr) were measured prospectively in ten pregnancies in eight allograft recipients before conception, throughout pregnancy, 8 to 12 weeks postpartum, and 4 to 6 monthly thereafter. Inulin (C1) and creatinine (Cr) clear-ances during infusion were also determined and protein excretion was evaluated. The results were compared to those in similar studies in ten healthy women. By the tenth gestational week 24-hr Ccr was 124(SD) 15.9 ml/min in healthy women (an increase of 38%: range, 18 to 69%) and in transplant patients was 105 28.1 mi/mm (an increase of 34%: range, 10 to 60%), with the greatest increments in those whose allografts functioned best before conception, regardless of donor source and sex or the transplant-pregnancy interval. In late pregnancy mean 24-hr Cc. decreased by 19%(range, 6 to 28%) in healthy women and by 34%(range, 12 to 57%) in the transplant patients, but in most this did not represent graft deterioration nor lead to permanent impairment. At all time points C1 values were 5 to 10% greater than those for 24-hr Ccr but slightly less than infusion CCr values. Protein excretion increased throughout pregnancy and by the third trimester in healthy women averaged 200 mg in 24 hr and regularly exceeded 500 mg in 24 hr in transplant patients, which was three times non-pregnant levels and probably not clinically significant. No definite pattern was evident regarding the effect of pregnancy on longterm renal prognosis but in eight of the ten pregnancies GFR had returned to pre-pregnancy values by 8 to 12 weeks postpartum. It can be concluded that renal allografts adapt to pregnancy normally and that reduced GFR and proteinuria in the third trimester are common but usually transient. Further studies are needed to answer questions on the effects of pregnancy on renal prognosis.
L'effet de Ia grossesse sur Ia fonction rénale de receveuses d'allogreffes rénales. Chez les femmes transplantées rénales, le debit de filtration glomerulaire (GFR) augmente au cours de Ia grossesse, mais la période a taquelle cette élévation se produit, ses relations avec GFR prégravidique et l'aspect global de cc changement sont inconnus. La clearance de la créatinine des vingt-quatre heures (24-hr Car) a été mesurëe prospectivement lors de dix grossesses chez huit receveuses d'allogreffe depuis avant la conception, pendant la grossesse, 8 a 12 semaines post-partum et 4 a 6 mois plus tard. Les clearances de l'inuline (C1,,) et de Ia créatinine (Ccr) sous perfusion ont egalement été déterminées, et l'excrCtion protéique a été évaluée. Les résultats ont été compares a ceux d'études similaires chez dix femmes normales. A Ia l0ème semaine de gestation, 24-hr C. était de 124(SD) 15, 9 mi/mm
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